Revision as of 16:09, 10 May 2024

Survival data

A Package for Survival Analysis in S by Terry M. Therneau, 1999
Survival Analysis in R Emily Zabor
https://web.stanford.edu/~lutian/coursepdf/stat331.HTML and https://web.stanford.edu/~lutian/coursepdf/ (3 types of tests).
http://www.stat.columbia.edu/~madigan/W2025/notes/survival.pdf.
- How to manually compute the KM curve and by R
- Estimation of parametric survival function from joint likelihood in theory and R.
http://data.princeton.edu/wws509/notes/c7s1.html
http://data.princeton.edu/pop509/ParametricSurvival.pdf Parametric survival models with covariates (logT = alpha + sigma W) p8
- Weibull p2 where T ~ Weibull and W ~ Extreme value.
- Gamma p3 where T ~ Gamma and W ~ Generalized extreme value
- Generalized gamma p4,
- log normal p4 where T ~ lognormal and W ~ N(0,1)
- log logistic p4 where T ~ log logistic and W ~ standard logistic distribution.
http://www.math.ucsd.edu/~rxu/math284/ (good cover) Wald test
http://www.stats.ox.ac.uk/~mlunn/
https://www.openintro.org/download.php?file=survival_analysis_in_R&referrer=/stat/surv.php
https://cran.r-project.org/web/packages/survival/vignettes/timedep.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065034/
Survival Analysis with R from rviews.rstudio.com
Survival Analysis with R from bioconnector.og.

Calculating survival time in R

base R and lubridate methods. Emily C. Zabor

Convert days to years or months

sx_date for surgery date

as.numeric(difftime(last_fup_date, sx_date, units = "days")) / 365.25

To convert days to months

days / (365.25/12)
# 365.25/12 = 30.4375

Overall survival, progression-free, recurrence-free survival

Overall survival. It is common to use diagnostic date or treatment/intervention starting date as the starting point. It is usually used as an indication of how well a treatment works. How is overall survival assessed in randomised clinical trials in cancer and are subsequent treatment lines considered? A systematic review
- Event: if a patient died (any cause), T=(date of death) - (date of therapy start)
- Censored: if a patient was still alive at last follow-up, T=(date of last follow-up) - (date of therapy start)

Progression-free survival

Recurrence-free survival (RFS)
- Event: if a patient relapsed or died. T=(date of relapse or dealth, whichever comes first) - (date of therapy/treatment start)
- Censored: if a patient had not relapsed and was still alive at last follow-up. T=(date of last follow-up) - (date of therapy start)

Disease-free survival (same as RFS)

Censoring

Sample schemes of incomplete data, Censoring in Clinical Trials: Review of Survival Analysis Techniques

Type I censoring: the censoring time is fixed
Type II censoring
Random censoring
- Right censoring
- Left censoring
Interval censoring
Truncation

The most common is called right censoring and occurs when a participant does not have the event of interest during the study and thus their last observed follow-up time is less than their time to event. This can occur when a participant drops out before the study ends or when a participant is event free at the end of the observation period.

Definitions of common terms in survival analysis

Event: Death, disease occurrence, disease recurrence, recovery, or other experience of interest
Time: The time from the beginning of an observation period (such as surgery or beginning treatment) to (i) an event, or (ii) end of the study, or (iii) loss of contact or withdrawal from the study.
Censoring / Censored observation: If a subject does not have an event during the observation time, they are described as censored. The subject is censored in the sense that nothing is observed or known about that subject after the time of censoring. A censored subject may or may not have an event after the end of observation time.

In R, "status" should be called event status. status = 1 means event occurred. status = 0 means no event (censored). Sometimes the status variable has more than 2 states. We can uses "status != 0" to replace "status" in Surv() function.

status=0/1/2 for censored, transplant and dead in survival::pbc data.
status=0/1/2 for censored, relapse and dead in randomForestSRC::follic data.

How to explore survival data

https://en.wikipedia.org/wiki/Survival_analysis#Survival_analysis_in_R

Create graph of length of time that each subject was in the study

library(survival)
# sort the aml data by time
aml <- aml[order(aml$time),]
with(aml, plot(time, type="h"))

File:Aml time.svg

Create the life table survival object

summary(aml.survfit)
Call: survfit(formula = Surv(time, status == 1) ~ 1, data = aml)

 time n.risk n.event survival std.err lower 95% CI upper 95% CI
    5     23       2   0.9130  0.0588       0.8049        1.000
    8     21       2   0.8261  0.0790       0.6848        0.996
    9     19       1   0.7826  0.0860       0.6310        0.971
   12     18       1   0.7391  0.0916       0.5798        0.942
   13     17       1   0.6957  0.0959       0.5309        0.912
   18     14       1   0.6460  0.1011       0.4753        0.878
   23     13       2   0.5466  0.1073       0.3721        0.803
   27     11       1   0.4969  0.1084       0.3240        0.762
   30      9       1   0.4417  0.1095       0.2717        0.718
   31      8       1   0.3865  0.1089       0.2225        0.671
   33      7       1   0.3313  0.1064       0.1765        0.622
   34      6       1   0.2761  0.1020       0.1338        0.569
   43      5       1   0.2208  0.0954       0.0947        0.515
   45      4       1   0.1656  0.0860       0.0598        0.458
   48      2       1   0.0828  0.0727       0.0148        0.462

Kaplan-Meier curve for aml with the confidence bounds.

plot(aml.survfit, xlab = "Time", ylab="Proportion surviving")

Create aml life tables broken out by treatment (x, "Maintained" vs. "Not maintained")

surv.by.aml.rx <- survfit(Surv(time, status == 1) ~ x, data = aml)

summary(surv.by.aml.rx)
Call: survfit(formula = Surv(time, status == 1) ~ x, data = aml)

                x=Maintained 
 time n.risk n.event survival std.err lower 95% CI upper 95% CI
    9     11       1    0.909  0.0867       0.7541        1.000
   13     10       1    0.818  0.1163       0.6192        1.000
   18      8       1    0.716  0.1397       0.4884        1.000
   23      7       1    0.614  0.1526       0.3769        0.999
   31      5       1    0.491  0.1642       0.2549        0.946
   34      4       1    0.368  0.1627       0.1549        0.875
   48      2       1    0.184  0.1535       0.0359        0.944

                x=Nonmaintained 
 time n.risk n.event survival std.err lower 95% CI upper 95% CI
    5     12       2   0.8333  0.1076       0.6470        1.000
    8     10       2   0.6667  0.1361       0.4468        0.995
   12      8       1   0.5833  0.1423       0.3616        0.941
   23      6       1   0.4861  0.1481       0.2675        0.883
   27      5       1   0.3889  0.1470       0.1854        0.816
   30      4       1   0.2917  0.1387       0.1148        0.741
   33      3       1   0.1944  0.1219       0.0569        0.664
   43      2       1   0.0972  0.0919       0.0153        0.620
   45      1       1   0.0000     NaN           NA           NA

Plot KM plot broken out by treatment

plot(surv.by.aml.rx, xlab = "Time", ylab="Survival",
     col=c("black", "red"), lty = 1:2, 
     main="Kaplan-Meier Survival vs. Maintenance in AML")
legend(100, .6, c("Maintained", "Not maintained"), 
     lty = 1:2, col=c("black", "red"))

Perform the log rank test using the R function survdiff().

surv.diff.aml <- survdiff(Surv(time, status == 1) ~ x, data=aml)
surv.diff.aml

Call:
survdiff(formula = Surv(time, status == 1) ~ x, data = aml)

                 N Observed Expected (O-E)^2/E (O-E)^2/V
x=Maintained    11        7    10.69      1.27       3.4
x=Nonmaintained 12       11     7.31      1.86       3.4

 Chisq= 3.4  on 1 degrees of freedom, p= 0.07

Summary statistics

Kaplan-Meier Method and Log-Rank Test
Statistics
- Table of status vs treatment (with proportion)
- Table of treatment vs training/test
Life table
- summary(survfit(Surv(time, status) ~ 1)) or summary(survfit(Surv(time, status) ~ treatment))
- KMsurv::lifetab()
Coxph function and visualize them using the ggforest package

Some public data

package	data (sample size)
survival	pbc (418), ovarian (26), aml/leukemia (23), colon (1858), lung (228), veteran (137)
pec	GBSG2 (686), cost (518)
randomForestSRC	follic (541)
KMsurv	A LOT. tongue (80)
survivalROC	mayo (312)
survAUC	NA

Kaplan & Meier and Nelson-Aalen: survfit.formula(), Surv()

Landmarks
- Kaplan-Meier: 1958
- Nelson: 1969
- Cox and Brewlow: 1972 S(t) = exp(-Lambda(t))
- Aalen: 1978 Lambda(t)
https://en.wikipedia.org/wiki/Kaplan%E2%80%93Meier_estimator
A practical guide to understanding Kaplan-Meier curves 2010
D distinct times [math]\displaystyle{ t_1 \lt t_2 \lt \cdots \lt t_D }[/math]. At time [math]\displaystyle{ t_i }[/math] there are [math]\displaystyle{ d_i }[/math] events. Let [math]\displaystyle{ Y_i }[/math] be the number of individuals who are at risk at time [math]\displaystyle{ t_i }[/math]. The quantity [math]\displaystyle{ d_i/Y_i }[/math] provides an estimate of the conditional probability that an individual who survives to just prior to time [math]\displaystyle{ t_i }[/math] experiences the event at time [math]\displaystyle{ t_i }[/math]. The KM estimator of the survival function and the Nelson-Aalen estimator of the cumulative hazard (their relationship is given below) are define as follows ([math]\displaystyle{ t_1 \le t }[/math]):

[math]\displaystyle{ \begin{align} \hat{S}(t) &= \prod_{t_i \le t} [1 - d_i/Y_i] \\ \hat{H}(t) &= \sum_{t_i \le t} d_i/Y_i \end{align} }[/math]

str(kidney)
'data.frame':	76 obs. of  7 variables:
$ id     : num  1 1 2 2 3 3 4 4 5 5 ...
$ time   : num  8 16 23 13 22 28 447 318 30 12 ...
$ status : num  1 1 1 0 1 1 1 1 1 1 ...
$ age    : num  28 28 48 48 32 32 31 32 10 10 ...
$ sex    : num  1 1 2 2 1 1 2 2 1 1 ...
$ disease: Factor w/ 4 levels "Other","GN","AN",..: 1 1 2 2 1 1 1 1 1 1 ...
$ frail  : num  2.3 2.3 1.9 1.9 1.2 1.2 0.5 0.5 1.5 1.5 ...
kidney[order(kidney$time), c("time", "status")]
kidney[kidney$time == 13, ] # one is dead and the other is alive
length(unique(kidney$time)) # 60

sfit <- survfit(Surv(time, status) ~ 1, data = kidney)

sfit
Call: survfit(formula = Surv(time, status) ~ 1, data = kidney)

      n  events  median 0.95LCL 0.95UCL 
     76      58      78      39     152 

str(sfit)
List of 13
$ n        : int 76
$ time     : num [1:60] 2 4 5 6 7 8 9 12 13 15 ...
$ n.risk   : num [1:60] 76 75 74 72 71 69 65 64 62 60 ...
$ n.event  : num [1:60] 1 0 0 0 2 2 1 2 1 2 ...
$ n.censor : num [1:60] 0 1 2 1 0 2 0 0 1 0 ...
$ surv     : num [1:60] 0.987 0.987 0.987 0.987 0.959 ...
$ type     : chr "right"
length(unique(kidney$time))  # [1] 60
all(sapply(sfit$time, function(tt) sum(kidney$time >= tt)) == sfit$n.risk) # TRUE
all(sapply(sfit$time, function(tt) sum(kidney$status[kidney$time == tt])) == sfit$n.event) # TRUE
all(sapply(sfit$time, function(tt) sum(1-kidney$status[kidney$time == tt])) == sfit$n.censor) #  TRUE
all(cumprod(1 - sfit$n.event/sfit$n.risk) == sfit$surv) #  FALSE
range(abs(cumprod(1 - sfit$n.event/sfit$n.risk) - sfit$surv))
# [1] 0.000000e+00 1.387779e-17

summary(sfit)
time n.risk n.event survival std.err lower 95% CI upper 95% CI
    2     76       1    0.987  0.0131      0.96155        1.000
    7     71       2    0.959  0.0232      0.91469        1.000
    8     69       2    0.931  0.0297      0.87484        0.991
 ...
  511      3       1    0.042  0.0288      0.01095        0.161
  536      2       1    0.021  0.0207      0.00305        0.145
  562      1       1    0.000     NaN           NA           NA

Understanding survival analysis: Kaplan-Meier estimate
Note that the KM estimate is left-continuous step function with the intervals closed at left and open at right. For [math]\displaystyle{ t \in [t_j, t_{j+1}) }[/math] for a certain j, we have [math]\displaystyle{ \hat{S}(t) = \prod_{i=1}^j (1-d_i/n_i) }[/math] where [math]\displaystyle{ d_i }[/math] is the number people who have an event during the interval [math]\displaystyle{ [t_i, t_{i+1}) }[/math] and [math]\displaystyle{ n_i }[/math] is the number of people at risk just before the beginning of the interval [math]\displaystyle{ [t_i, t_{i+1}) }[/math].
The product-limit estimator can be constructed by using a reduced-sample approach. We can estimate the [math]\displaystyle{ P(T \gt t_i | T \ge t_i) = \frac{Y_i - d_i}{Y_i} }[/math] for [math]\displaystyle{ i=1,2,\cdots,D }[/math]. [math]\displaystyle{ S(t_i) = \frac{S(t_i)}{S(t_{i-1})} \frac{S(t_{i-1})}{S(t_{i-2})} \cdots \frac{S(t_2)}{S(t_1)} \frac{S(t_1)}{S(0)} S(0) = P(T \gt t_i | T \ge t_i) P(T \gt t_{i-1} | T \ge t_{i-1}) \cdots P(T\gt t_2|T \ge t_2) P(T\gt t_1 | T \ge t_1) }[/math] because S(0)=1 and, for a discrete distribution, [math]\displaystyle{ S(t_{i-1}) = P(T \gt t_{i-1}) = P(T \ge t_i) }[/math].
Self consistency. If we had no censored observations, the estimator of the survival function at a time t is the proportion of observations which are larger than t, that is, [math]\displaystyle{ \hat{S}(t) = \frac{1}{n}\sum I(X_i \gt t) }[/math].
Curves are plotted in the same order as they are listed by print (which gives a 1 line summary of each). For example, -1 < 1 and 'Maintenance' < 'Nonmaintained'. That means, the labels list in the legend() command should have the same order as the curves.
Kaplan and Meier is used to give an estimator of the survival function S(t)
Nelson-Aalen estimator is for the cumulative hazard H(t). Note that [math]\displaystyle{ 0 \le H(t) \lt \infty }[/math] and [math]\displaystyle{ H(t) \rightarrow \infty }[/math] as t goes to infinity. So there is a constraint on the hazard function, see Wikipedia.

Note that S(t) is related to H(t) by [math]\displaystyle{ H(t) = -ln[S(t)] }[/math] or [math]\displaystyle{ S(t) = exp[-H(t)] }[/math]. The two estimators are similar (see example 4.1A and 4.1B from Klein and Moeschberge).

The Nelson-Aalen estimator has two primary uses in analyzing data

Selecting between parametric models for the time to event
Crude estimates of the hazard rate h(t). This is related to the estimation of the survival function in Cox model. See 8.6 of Klein and Moeschberge.

The Kaplan–Meier estimator (the product limit estimator) is an estimator for estimating the survival function from lifetime data. In medical research, it is often used to measure the fraction of patients living for a certain amount of time after treatment.

Note that

The "+" sign in the KM curves means censored observations (this convention matches with the output of Surv() function) and a long vertical line (not '+') means there is a dead observation at that time.

> aml[1:5,]
  time status          x
1    9      1 Maintained
2   13      1 Maintained
3   13      0 Maintained
4   18      1 Maintained
5   23      1 Maintained
> Surv(aml$time, aml$status)[1:5,]
[1]  9  13  13+ 18  23

If the last observation (longest survival time) is dead, the survival curve will goes down to zero. Otherwise, the survival curve will remain flat from the last event time.

Usually the KM curve of treatment group is higher than that of the control group.

The Y-axis (the probability that a member from a given population will have a lifetime exceeding time) is often called

Cumulative probability
Cumulative survival
Percent survival
Probability without event
Proportion alive/surviving
Survival
Survival probability

File:KMcurve.png, File:KMannotation.png, File:KMcurve cumhaz.png

> library(survival)
> str(aml$x)
 Factor w/ 2 levels "Maintained","Nonmaintained": 1 1 1 1 1 1 1 1 1 1 ...
> plot(leukemia.surv <- survfit(Surv(time, status) ~ x, data = aml[7:17,] ) , 
      lty=2:3, mark.time = TRUE) # a (small) subset, mark.time is used to show censored obs
> aml[7:17,]
   time status             x
7    31      1    Maintained
8    34      1    Maintained
9    45      0    Maintained
10   48      1    Maintained
11  161      0    Maintained
12    5      1 Nonmaintained
13    5      1 Nonmaintained
14    8      1 Nonmaintained
15    8      1 Nonmaintained
16   12      1 Nonmaintained
17   16      0 Nonmaintained
> legend(100, .9, c("Maintenance", "No Maintenance"), lty = 2:3) # lty: 2=dashed, 3=dotted
> title("Kaplan-Meier Curves\nfor AML Maintenance Study") 

# Cumulative hazard plot
# Lambda(t) = -log(S(t)); 
# see https://en.wikipedia.org/wiki/Survival_analysis
# http://statweb.stanford.edu/~olshen/hrp262spring01/spring01Handouts/Phil_doc.pdf
plot(leukemia.surv <- survfit(Surv(time, status) ~ x, data = aml[7:17,] ) , 
      lty=2:3, mark.time = T, fun="cumhaz", ylab="Cumulative Hazard")

Kaplan-Meier estimator from the wikipedia.
Two papers this and this to describe steps to calculate the KM estimate.
Estimating a survival probability in R

# https://www.lexjansen.com/pharmasug/2011/CC/PharmaSUG-2011-CC16.pdf
mydata <- data.frame(time=c(3,6,8,12,12,21),status=c(1,1,0,1,1,1))
km <- survfit(Surv(time, status)~1, data=mydata)
plot(km, mark.time = T)
survest <- stepfun(km$time, c(1, km$surv))
plot(survest)
> str(km)
List of 13
 $ n        : int 6
 $ time     : num [1:5] 3 6 8 12 21
 $ n.risk   : num [1:5] 6 5 4 3 1
 $ n.event  : num [1:5] 1 1 0 2 1
 $ n.censor : num [1:5] 0 0 1 0 0
 $ surv     : num [1:5] 0.833 0.667 0.667 0.222 0
 $ type     : chr "right"
 $ std.err  : num [1:5] 0.183 0.289 0.289 0.866 Inf
 $ upper    : num [1:5] 1 1 1 1 NA
 $ lower    : num [1:5] 0.5827 0.3786 0.3786 0.0407 NA
 $ conf.type: chr "log"
 $ conf.int : num 0.95
> class(survest)
[1] "stepfun"  "function"
> survest
Step function
Call: stepfun(km$time, c(1, km$surv))
 x[1:5] =      3,      6,      8,     12,     21
6 plateau levels =      1, 0.83333, 0.66667,  ..., 0.22222,      0
> str(survest)
function (v)  
 - attr(*, "class")= chr [1:2] "stepfun" "function"
 - attr(*, "call")= language stepfun(km$time, c(1, km$surv))

File:Kmcurve_toy.svg

Multiple curves

Curves/groups are ordered. The first color in the palette is used to color the first level of the factor variable. This is same idea as ggsurvplot in the survminer package. This affects parameters like col and lty in plot() function. For example,

1<2
'c' < 't'
'control' < 'treatment'
'Control' < 'Treatment'
'female' < 'male'.

For legend(), the first category in legend argument will appear at the top of the legend box.

library(RColorBrewer)
library(survival)
set1 = c(brewer.pal(9,"Set1"), brewer.pal(8, "Dark2"))

fit <- survfit(Surv(futime, fustat) ~ cut(age, quantile(age, seq(0,1,l=4))), data = ovarian) 
plot(fit, col = set1[3:1])
par(xpd=TRUE)
legend(x=800, y=1.1, bty="n", "Risk", cex=0.9, text.font=2)
legend(x=800, y=1.0, bty="n", text.col = set1[3:1], c("Low","Intermediate","High"), cex=0.9)

Continuous predictor

There could be several reasons why we might want to consider Kaplan-Meier (KM) curves using a continuous covariate:

Visualizing Survival Differences: KM curves can help visualize survival differences across different levels of a continuous covariate. For example, if the covariate is age, we might be interested in how survival probabilities differ across various age groups.
Detecting Non-Proportional Hazards: KM curves can help detect non-proportional hazards, which occur when the hazard ratios between groups change over time. This can be particularly useful when dealing with continuous covariates, as the relationship between the covariate and survival may not be constant over time.
Understanding the Effect of Covariates: KM curves can provide insights into the effect of continuous covariates on survival time. This can be useful in understanding the impact of treatment dosage, biomarker levels, or other continuous measures on patient survival.
Developing Diagnostic Tools: Some researchers have proposed methods to create KM-type curves for continuous covariates as diagnostic tools. These tools can help visualize the confounder-adjusted effect of continuous variables on a time-to-event outcome.

The Kaplan-Meier estimator is a (non-parametric) univariable method, meaning it approximates the survival function using at most one variable/predictor. When you have a continuous predictor, one common approach is to convert the continuous variable into a categorical variable by creating groups. This can be done by determining cut-points, such as using the median of the predictor as the group’s cut point.

However, this approach has its limitations. The choice of cut-point can greatly influence the results, and arbitrary cut-points may lead to loss of information. Moreover, this method does not adjust for possible confounders.

Estimating x-year probability of survival

Survival Analysis in R. See the explanation there why the “naive” estimate is wrong when we ignore censoring? Correct is 41% but naive is 47%.

plot(survfit(Surv(time, status) ~ 1, data = lung))
summary(survfit(Surv(time, status) ~ 1, data = lung), times = c(200, 400, 600))

This is useful when we want to compare difference in (overall) survival probability at (5) years based on (A model) (high/low risk groups were defined by the median of scores of the training data).

xlab, ylab

Survival probability, Time since diagnosis (year)
OS probability, Time to death (months)
RFS probability, Time to relapse or death (months)

Median survival and 95% CI

median survival definition

The length of time from either the date of diagnosis or the start of treatment for a disease, such as cancer, that half of the patients in a group of patients diagnosed with the disease are still alive. In a clinical trial, measuring the median survival is one way to see how well a new treatment works. Also called median overall survival. See cancer.gov
The middle point of longevity of a population: an equal number of people live longer than the median as the number of people who die earlier than the median thefreedictionary
Median Survival or Mean Survival: Which Measure Is the Most Appropriate for Patients, Physicians, and Policymakers?
The median survival time is the time point at which the probability of survival equals 50%. See GraphPad
The average (?) survival time, which we quantify using the median. Survival times are not expected to be normally distributed so the mean is not an appropriate summary.
What happens if a survival curve doesn't reach 0.5? It means you can't compute the median.

survfit(Surv(time, status) ~ 1, data). Note the "naive" estimate is wrong (median survival time among patients who died). Correct is 310 but naive is 226.

R> survfit(Surv(time, status) ~ 1, data = lung) # correct
Call: survfit(formula = Surv(time, status) ~ 1, data = lung)

       n events median 0.95LCL 0.95UCL
[1,] 228    165    310     285     363
R> lung %>% 
     filter(status == 1) %>% 
     summarize(median_surv = median(time)) # wrong
  median_surv
1         284
R> median(lung$time) # wrong
[1] 255.5

R> survfit(Surv(time, status) ~ 1, data = aml)
Call: survfit(formula = Surv(time, status) ~ 1, data = aml)

      n events median 0.95LCL 0.95UCL
[1,] 23     18     27      18      45

R> survfit(Surv(time, status) ~ x, data = aml)
Call: survfit(formula = Surv(time, status) ~ x, data = aml)

                 n events median 0.95LCL 0.95UCL
x=Maintained    11      7     31      18      NA
x=Nonmaintained 12     11     23       8      NA

# Extract the median survival time
R> library(survMisc)
R> fit <- survfit(Surv(time, status) ~ 1, data = lung) 
R> median_survival_time <- median(fit)
 50 
310

Restricted mean survival time

Restricted mean survival time: an alternative to the hazard ratio for the design and analysis of randomized trials with a time-to-event outcome Royston 2013
The Use of Restricted Mean Survival Time (RMST) Method When Proportional Hazards Assumption is in Doubt
- To estimate treatment effect for time to event, Hazard Ratio (HR) is commonly used.
- HR is often assumed to be constant over time (i.e., proportional hazard assumption).
- Recently, we have some doubt about this assumption.
- If the PH assumption does not hold, the interpretation of HR can be difficult.
RMST is defined as the area under the survival curve up to t* (truncated time or horizon), which should be pre-specified for a randomized trial. Uno 2014

survival::print.survfit(). How to compute the mean survival time.

fit <- survfit(Surv(time, status == 1) ~ x, data = aml)
print(fit, print.rmean=TRUE) # assume the longest survival time is the horizon
#                  n events rmean* se(rmean) median 0.95LCL 0.95UCL
# x=Maintained    11      7   52.6     19.83     31      18      NA
# x=Nonmaintained 12     11   22.7      4.18     23       8      NA
#     * restricted mean with upper limit =  161 
print(fit, print.rmean=TRUE, rmean=250)
#                  n events rmean* se(rmean) median 0.95LCL 0.95UCL
# x=Maintained    11      7   27.4      3.01     31      18      NA
# x=Nonmaintained 12     11   21.2      3.53     23       8      NA
#     * restricted mean with upper limit =  36 

# To extract the RMST values
survival:::survmean(fit, rmean=36)[[1]][, "rmean"]
#    x=Maintained x=Nonmaintained 
#        27.42500        21.15278

survRM2 package

PWEALL:: rmsth()

R> library(survRM2)
R> D = rmst2.sample.data()
R> nrow(D)
[1] 312
R> head(D[,1:3])
       time status arm
1  1.095140      1   1
2 12.320329      0   1
3  2.770705      1   1
4  5.270363      1   1
5  4.117728      0   0
6  6.852841      1   0
R> time   = D$time
R> status = D$status
R> arm    = D$arm
R> rmst2(time, status, arm, tau=10)

The truncation time: tau = 10  was specified. 

Restricted Mean Survival Time (RMST) by arm 
              Est.    se lower .95 upper .95
RMST (arm=1) 7.146 0.283     6.592     7.701
RMST (arm=0) 7.283 0.295     6.704     7.863


Restricted Mean Time Lost (RMTL) by arm 
              Est.    se lower .95 upper .95
RMTL (arm=1) 2.854 0.283     2.299     3.408
RMTL (arm=0) 2.717 0.295     2.137     3.296


Between-group contrast 
                       Est. lower .95 upper .95     p
RMST (arm=1)-(arm=0) -0.137    -0.939     0.665 0.738
RMST (arm=1)/(arm=0)  0.981     0.878     1.096 0.738
RMTL (arm=1)/(arm=0)  1.050     0.787     1.402 0.738

R> library(PWEALL)
R> PWEALL::rmsth(time, status, tcut=10)
$tcut
[1] 10
$rmst
[1] 7.208579
$var
[1] 13.00232
$vadd
[1] 3.915123

R> PWEALL::rmsth(time[arm == 0], status[arm ==0], tcut=10)
$tcut
[1] 10
$rmst
[1] 7.283416
$var
[1] 13.30564
$vadd
[1] 3.73545

R> PWEALL::rmsth(time[arm == 1], status[arm ==1], tcut=10)
$tcut
[1] 10
$rmst
[1] 7.146493
$var
[1] 12.49073
$vadd
[1] 3.967705

surv2sampleComp, 生存曲線下面積RMST(Restricted mean survival time)
Clustered restricted mean survival time regression Chen, 2022

Inverse Probability of Weighting

https://en.wikipedia.org/wiki/Inverse_probability_weighting
Robust Inference Using Inverse Probability Weighting, pdf
The intuition behind inverse probability weighting in causal inference
Idea:
- Inverse Probability of Weighting (IPW) is a statistical technique used in causal inference to adjust for the bias introduced by non-random sampling or missing data. IPW is used to estimate the population average treatment effect from observational data, by weighting the contribution of each individual in the sample based on their probability of receiving the treatment or being observed.
- The basic idea behind IPW is to use the observed covariates to infer the probabilities of treatment assignment or missing data, and then use these probabilities as weights to correct for the bias in the sample. By doing so, IPW allows for estimation of treatment effects as if the sample were randomly assigned, and it provides a consistent estimate of the population average treatment effect under certain assumptions.
Example:
- Suppose we want to study the effect of a new drug on blood pressure. We collect data from a sample of patients, but some of them do not take the drug as prescribed, and others drop out of the study before it ends. We want to use this sample to estimate the average treatment effect of the drug on blood pressure.
- To do this using IPW, we first need to estimate the probability of receiving the treatment (i.e., taking the drug as prescribed) and the probability of being observed (i.e., not dropping out of the study) for each patient. We can use logistic regression or other methods to estimate these probabilities based on the patient's covariates (e.g., age, sex, baseline blood pressure, etc.).
- Once we have these probabilities, we can use them as weights to adjust for the bias introduced by non-random treatment assignment and missing data. For each patient, we multiply their outcome (blood pressure) by the inverse of their probability of receiving the treatment and being observed, and then take the weighted average over the sample. This gives us an estimate of the average treatment effect of the drug on blood pressure that corrects for the bias introduced by non-random sampling and missing data.
Numerical example
- Suppose we have a sample of 100 patients, and we observe the following: 1) 40 patients take the drug as prescribed and have a mean blood pressure reduction of 10 mmHg. 2) 30 patients do not take the drug as prescribed and have a mean blood pressure reduction of 5 mmHg. 3) 20 patients drop out of the study before it ends and have a mean blood pressure reduction of 7 mmHg. 4) 10 patients both take the drug as prescribed and complete the study, and have a mean blood pressure reduction of 12 mmHg.
- To estimate the average treatment effect of the drug on blood pressure using IPW, we first need to estimate the probability of receiving the treatment (i.e., taking the drug as prescribed) and the probability of being observed (i.e., not dropping out of the study) for each patient. For simplicity, let's assume that these probabilities are equal for all patients.
- Suppose
  1. For the 40 patients who took the drug as prescribed: Weight = 1 / 0.5 = 2, Weighted outcome = 2 * 10 = 20,
  2. For the 30 patients who did not take the drug as prescribed: Weight = 1 / 0.5 = 2, Weighted outcome = 2 * 5 = 10,
  3. For the 20 patients who dropped out of the study: Weight = 1 / 0.5 = 2, Weighted outcome = 2 * 7 = 14,
  4. For the 10 patients who both took the drug as prescribed and completed the study: Weight = 1 / 0.5 = 2. Weighted outcome = 2 * 12 = 24
- IPW estimate of average treatment effect = (20 + 10 + 14 + 24) / 100 = 9.8 mmHg. This IPW estimate of 9.8 mmHg suggests that, on average, the drug reduces blood pressure by 9.8 mmHg. This estimate corrects for the bias introduced by non-random treatment assignment and missing data.
- What is 0.5 when we calculate the weight in the above example?
  - In the numerical example I provided earlier, the value of 0.5 used in the weight calculation represents the estimated probability of receiving the treatment (i.e., taking the drug as prescribed) and the probability of being observed (i.e., not dropping out of the study) for each patient.
  - For simplicity, I assumed that these probabilities are equal for all patients and equal to 0.5 in the example. This is often not the case in real-world data, and these probabilities need to be estimated using methods such as logistic regression or propensity score.
  - The weight for each patient is then calculated as the inverse of these probabilities: Weight = 1 / probability of receiving the treatment and being observed
  - So, in the example, the weight for each patient is equal to 1 / 0.5 = 2. This weight represents the importance of each patient in the IPW estimate of the average treatment effect.
- The weights in IPW are usually obtained using one of the following methods:
  1. Logistic Regression: This is a common method for estimating the weights in IPW. We use logistic regression to estimate the probability of receiving the treatment or being observed as a function of the patient's covariates. The coefficients from the logistic regression model are then used to calculate the weights for each patient.
  2. Propensity Score: This is another common method for estimating the weights in IPW. The propensity score is defined as the probability of receiving the treatment given the patient's covariates. We can estimate the propensity score using logistic regression or other methods, and then use it to calculate the weights for each patient.
  3. Weight Truncation: This is a method to stabilize the weights in IPW, especially when some of the weights are very large. Weight truncation involves replacing the weights that are larger than a certain threshold with the threshold. This reduces the influence of outliers on the IPW estimate and helps to prevent over-fitting.
  4. Other Methods: There are also other methods for estimating the weights in IPW, such as the Bayesian Hierarchical Modeling and the Kernel Density Estimation. These methods are more complex but can provide more accurate and flexible estimates of the weights, especially when the relationship between the treatment and the covariates is non-linear.

Mathematical formula for IPW
- Let Y be the outcome of interest (e.g., a continuous or binary variable), T be the treatment indicator (e.g., 0 for control group and 1 for treatment group), X be a vector of covariates, and W be the weight for each individual i. The IPW estimate of the average treatment effect (ATE) is given by:[math]\displaystyle{ ATE = E[Y|T=1] - E[Y|T=0] }[/math]
where E[Y|T=1] and E[Y|T=0] are the expected values of Y for the treated and control groups, respectively. These expected values can be estimated using the weighted sample mean as follows
[math]\displaystyle{ \begin{align} E[Y|T=1] &= (1/N1) * Σ(W_i * Y_i) \text{ for i in treatment group} \\ E[Y|T=0] &= (1/N0) * Σ(W_i * Y_i) \text{ for i in control group} \end{align} }[/math]

where [math]\displaystyle{ N1 }[/math] and [math]\displaystyle{ N0 }[/math] are the number of individuals in the treatment and control groups, respectively, and [math]\displaystyle{ W_i }[/math] is the weight for individual [math]\displaystyle{ i }[/math].
- The weights [math]\displaystyle{ W_i }[/math] are usually estimated using one of the methods discussed earlier (e.g., logistic regression, propensity score, etc.). The IPW estimate of the ATE is unbiased if the weights are correctly estimated and if the distribution of the covariates X is well-balanced between the treatment and control groups.
- It is important to note that IPW is a complex method that requires careful estimation of the weights and assessment of the assumptions of the model. It is also sensitive to the choice of the covariates X and the model used to estimate the weights. Therefore, it is important to carefully evaluate the validity and robustness of the IPW estimate before drawing any conclusions.

Inverse Probability of Censoring Weighting (IPCW)

R packages
- kmcens() from survC1 package
- get.censoring.weights() from TreatmentSelection package (not sure)
- pec:ipcw() Estimation of censoring probabilities
- timeROC Time-dependent ROC curve estimation
- ipw: An R Package for Inverse Probability Weighting 2011
Consistent Estimation of the Expected Brier Score in General Survival Models with Right‐Censored Event Times Gerds et al 2006.
Inverse probability weighting https://www.bmj.com/content/352/bmj.i189 Examples are considered.
Correcting for Noncompliance and Dependent Censoring in an AIDS Clinical Trial with Inverse Probability of Censoring Weighted (IPCW) Log‐Rank Tests by James M. Robins, Biometrics 2000.
The Kaplan–Meier Estimator as an Inverse-Probability-of-Censoring Weighted Average by Satten 2001. IPCW.
IPCW https://www.math.leidenuniv.nl/scripties/MasterWillems.pdf#page=41
ipcwswitch: An R package for inverse probability of censoring weighting with an application to switches in clinical trials
The c-index is not proper for the evaluation of $t$-year predicted risks Blanche 2018. the IPCW c-index can be larger or smaller than IPCW AUC(t) depending on t.
Adapting machine learning techniques to censored time-to-event health record data: A general-purpose approach using inverse probability of censoring weighting Vock 2016. Referred in Kaplan-Meier IPCW.

The plots below show by flipping the status variable, we can accurately recover the survival function of the censoring variable. See the R code here for superimposing the true exponential distribution on the KM plot of the censoring variable.

require(survival)
n = 10000
beta1 = 2; beta2 = -1
lambdaT = 1 # baseline hazard
lambdaC = 2  # hazard of censoring
set.seed(1234)
x1 = rnorm(n,0)
x2 = rnorm(n,0)
# true event time
# T = rweibull(n, shape=1, scale=lambdaT*exp(-beta1*x1-beta2*x2)) # Wrong
T = Vectorize(rweibull)(n=1, shape=1, scale=lambdaT*exp(-beta1*x1-beta2*x2))

# method 1: exponential censoring variable
C <- rweibull(n, shape=1, scale=lambdaC)   
time = pmin(T,C)  
status <- 1*(T <= C) 
mean(status)
summary(T)
summary(C)
par(mfrow=c(2,1), mar = c(3,4,2,2)+.1)
status2 <- 1-status
plot(survfit(Surv(time, status2) ~ 1), 
     ylab="Survival probability",
     main = 'Exponential censoring time')

# method 2: uniform censoring variable
C <- runif(n, 0, 21)
time = pmin(T,C)  
status <- 1*(T <= C) 
status2 <- 1-status
plot(survfit(Surv(time, status2) ~ 1), 
     ylab="Survival probability",
     main = "Uniform censoring time")

File:Ipcw.svg

Numerical example
- Suppose we have a sample of 100 patients and we are interested in estimating the mean survival time. We observe the survival times for 80 of the patients and 20 are censored, meaning that the event of interest (death in this case) has not occurred at the time of data collection.
- Let's assume that we have estimated the probability of censoring for each individual using a logistic regression model. The probabilities are given by:
```
Individual 1: p_1 = 0.1
Individual 2: p_2 = 0.2
...
Individual 100: p_100 = 0.05
```
- The IPCW weights for each individual are then calculated as the inverse of the probability of censoring:
```
Individual 1: w_1 = 1 / p_1 = 1 / 0.1 = 10
Individual 2: w_2 = 1 / p_2 = 1 / 0.2 = 5
...
Individual 100: w_100 = 1 / p_100 = 1 / 0.05 = 20
```
- The IPCW estimate of the mean survival time is then calculated as the weighted average of the survival times, where the weights are the IPCW weights:
```
IPCW estimate = (w_1 * survival time of individual 1 + w_2 * survival time of individual 2 + ... + w_100 * survival time of individual 100) / (w_1 + w_2 + ... + w_100)
```
- The IPCW estimate takes into account the probability of censoring for each individual, and it gives more weight to individuals who are at higher risk of censoring, which can help to reduce the bias in the estimated mean survival time.

stepfun() and plot.stepfun()

Draw cumulative hazards using stepfun()
For KM curve case, see an example above.

GGally package (ggplot object)

ggsurv() from the GGally package. GGally has 2 times downloaded of survminer & more authors.

Advantage: return object class is c("gg", "ggplot") while survminer::ggsurvplot returns object class "ggsurvplot" "ggsurv", "list".

It seems to be better to apply order.legend = FALSE if we want the default color palette has the same order as the levels. For example

data(lung, package = "survival")
sf.sex <- survival::survfit(Surv(time, status) ~ sex, data = lung)
ggsurv(sf.sex)   # 2 = Salmon, 1 = Iris blue
                 # Colors are defined by the final survival time

ggsurv(sf.sex, order.legend = FALSE) # 1 = Salmon, 2 = Iris blue
                        # More consistent with what we expect
                        # Colors are defined by the levels

# More options
ggsurv(sf.sex, order.legend = FALSE, surv.col = scales::hue_pal()(2))

To combine multiple ggplot2 plots, use the ggpubr package. gridExtra is not developed after 2017.

library(GGally)
library(survival)
data(lung, package = "survival")
sf.lung <- survfit(Surv(time, status) ~ sex, data = lung)
p1 <- ggsurv(sf.lung, plot.cens = FALSE, lty.est = c(1, 3), size.est = 0.8, 
             xlab = "Time", ylab = "Survival", main = "Lower score")
p1 <- p1 + annotate("text", x=0, y=.25, hjust=0, label="zxcvb")
p2 <- ggsurv(sf.lung, plot.cens = FALSE, lty.est = c(1, 3), size.est = 0.8, 
             xlab = "Time", ylab = "Survival", main = "High score")
p2 <- p2 + annotate("text", x=0, y=.25, hjust=0, label="asdfg")

# gridExtra::grid.arrange(p1, p2, ncol=2, nrow =1) # no common legend option
ggpubr::ggarrange(p1, p2,  common.legend = TRUE, legend = "right")
# return object class: "gg"   "ggplot"    "ggarrange"

Survival curves with number at risk at bottom: survminer package

R function survminer::ggsurvplot()

survminer Cheatsheet by RStudio. It includes KM curves (ggsurvplot), diagnostics (ggcoxdiagnostics) and summary of Cox model (ggforest).
Survival Analysis Basics
ggsurvplot()
- ggsurvplot_facet() - if we want to create KM curves based subset of data (one plot)
- ggsurvplot_group_by() - if we want to create KM curves based subset of data (separate plots)
- ggsurvplot_list() - if we want to create a list of KM curves (practical application?)
- ggsurvplot_combine() - if we want to combine OS and PFS for example in one plot
Error: object of type 'symbol' is not subsettable. Use survminer::surv_fit() in lieu of survival::survfit()
- This is needed if we want to separate Surv() (formula) and survfit() in two statements. For instance, if we want to fit the same data with different formulas.
- surv_fit()
To save ggsurvplot(), use ggsave(FILE, res$plot) . To save arrange_ggsurvplots(), use ggsave(FILE, res)
http://www.sthda.com/english/wiki/survminer-r-package-survival-data-analysis-and-visualization
ggpubr: Publication Ready Plots
Cheatsheet
http://r-addict.com/2016/05/23/Informative-Survival-Plots.html
Add the numbers at risk table. cowplot::plot_grid() was used to combine the KM plot and risk table together.

Adjusting for covariates under non-proportional hazards. break.x.by or break.time.by to control x axis breaks.

survminer::ggsurvplot(, risk.table = TRUE, 
                      break.x.by = 6,
                      legend.title = "",
                      xlab = "Time (months)",
                      ylab = "Overall survival",
                      risk.table.fontsize = 4,
                      legend = c(0.8,0.8)))

library(survminer)
ggsurvplot(survo, risk.table = TRUE, pval=TRUE, pval.method = TRUE, 
           palette = c("#F8766D", "#00BFC4")) # (Salmon, Iris Blue)

Arrange ggsurv plots with one shared legend. Note we can add a title to a corner of an individual plot by a trick ggsurvplot()$plot + labs(title = "A") .
Arranging Multiple ggsurvplots arrange_ggsurvplots(). When I need to put two KM curves plot side by side using arrange_ggsurvplots(), some issues came out (these properties seem to inherit from arrangeGrob):
- if I try it on a terminal the function will open two graph devices and the first one is blank?
- if I try it on a terminal with print = FALSE option, it still open a blank graph window,
- if I try it in RStudio, the plot is not generated in RStudio but in a separate X window. It does not matter I am using macOS or Linux.
- if I just draw a plot from ggsurvplot(), the plot is drawn in RStudio as we want.
- ggpubr::ggarrange() is an alternative to arrange_ggsurvplots() but ggpubr::ggarrange() does not work with ggsurvplot() objects.
- survminer::ggsurvplot_combine() will put two curves in one plot.
- Solution: using the patchwork package. A single legend for multiple ggsurvplots using arrange_ggsurvplot
```
library(patchwork)
res1 <- ggsurvplot()
...
res1$plot + res2$plot + res3$plot + res4$plot + plot_layout(nrow=2, byrow = FALSE)
```

Add custom annotation to ggsurvplot. However, even I use the same x-value in ggsurvplot(pval.coord) and ggplot2::annotate(x), the texts are not aligned in x-axis.

ggsurv$plot <- ggsurv$plot+ 
              ggplot2::annotate("text", 
                                x = 100, y = 0.2, # x and y coordinates of the text
                                label = "My label", size=1)

Paper examples

High-dimensional single-cell analysis predicts response to anti-PD-1 immunotherapy

Questions:

How to remove tick mark on censored observations especially the case with a large sample size?

finalfit R package:

surv_plot() function

ggfortify

ggfortify: Data Visualization Tools for Statistical Analysis Results
Beneath and Beyond the Cox Model

ggsurvfit

ggsurvfit: Easy and Flexible Time-to-Event Figures

KMunicate

https://cran.r-project.org/web/packages/KMunicate/index.html

Life table

Re-construct survival data from KM curves

reconstructKM package

Calculation by hand

What is survival analysis? Examples by hand and in R

Compare the KM curve to the Cox model curve

Publication examples

FACT cohort patient survival analyses stratified by HRD status

Alternatives to survival function plot

https://www.rdocumentation.org/packages/survival/versions/2.43-1/topics/plot.survfit The fun argument, a transformation of the survival curve

fun = "event" or "F": f(y) = 1-y; it calculates P(T < t). This is like a t-year risk (Blanche 2018).
fun = "cumhaz": cumulative hazard function (f(y) = -log(y)); it calculates H(t). See Intuition for cumulative hazard function.

Breslow estimate

http://support.sas.com/documentation/cdl/en/statug/68162/HTML/default/viewer.htm#statug_lifetest_details03.htm
Breslow estimate is the exponentiation of the negative Nelson-Aalen estimate of the cumulative hazard function

Logrank/log-rank/log rank test

Logrank test is a hypothesis test to compare the survival distributions of two samples. The logrank test statistic compares estimates of the hazard functions of the two groups at each observed event time.
Statistics Notes - The logrank test 2004
- Calculation and an example data are provided.
- It is also possible to test for a trend in survival across ordered groups.
- The logrank test is based on the same assumptions as the Kaplan Meier survival curve - namely, that censoring is unrelated to prognosis, the survival probabilities are the same for subjects recruited early and late in the study, and the events happened at the times specified.
- The logrank test is most likely to detect a difference between groups when the risk of an event is consistently greater for one group than another. It is unlikely to detect a difference when survival curves cross, as can happen when comparing a medical with a surgical intervention.

STAT331 Course notes
Score test from the Cox regression is also labeled as logrank test. Logrank p-value for >2 groups.

?coxph
test1 <- list(time=c(4,3,1,1,2,2,3), 
              status=c(1,1,1,0,1,1,0), 
              x=c(0,2,1,1,1,0,0), 
              sex=c(0,0,0,0,1,1,1))
summary(coxph(Surv(time, status) ~ x, test1) )
# Call:
# coxph(formula = Surv(time, status) ~ x, data = test1)
#
#   n= 7, number of events= 5 
#
#     coef exp(coef) se(coef)     z Pr(>|z|)
# x 0.4608    1.5853   0.5628 0.819    0.413
#
#  exp(coef) exp(-coef) lower .95 upper .95
# x     1.585     0.6308    0.5261     4.777
#
# Concordance= 0.643  (se = 0.135 )
# Likelihood ratio test= 0.66  on 1 df,   p=0.4
# Wald test            = 0.67  on 1 df,   p=0.4
# Score (logrank) test = 0.71  on 1 df,   p=0.4

survdiff, Extract p-value from survdiff

sdf <- survdiff(Surv(time, status) ~ treatment, data=mydf)
pvalue <- 1 - pchisq(sdf$chisq, length(sdf$n) - 1)

On null hypotheses in survival analysis Stensrud 2019
Efficiency of two sample tests via the restricted mean survival time for analyzing event time observations Tian 2017
Stratified log-rank tests
survival package has a strata function that we can use in the survdiff() function.
- Differentiate group and strata
- The strata is useful when we suspect there is a confounding factor
Log-rank Test: When does it Fail and how to fix it
Survival Analysis: Logrank Test
Comparing Survival Curves
Survival analysis using a 5‐step stratified testing and amalgamation routine (5‐STAR) in randomized clinical trials by Mehrotra 2020

Logrank test vs Cox model

Logrank test vs Cox model.
- The cox model relies on the proportional hazards assumption. The logrank test does not. If your data are not consistent with the proportional hazards assumption, then the cox results may not be valid.
- the graph you show does not seem consistent with the proportional hazards assumption.
Logrank test relationship to other statistics & assumptions from wikipedia.
The logrank test statistic is equivalent to the score of a Cox regression. Is there an advantage of using a logrank test over a Cox regression? Since the log-rank test is a special case of the Cox model, it does not have fewer assumptions or more power. IMHO we no longer need to be using or teaching the log-rank test. Answered by Frank Harrell.
- The log-rank Test Assumes More Than the Cox Model. Numerical examples were given.
- I can confirm the log-rank tests and Cox regression pvalues are very close by using median as a cutoff from one data with 7288 proteins. The scatterplot shows both p-values are on a 45 degree line and the p-values distribution is like Uniform.
Kaplan-Meier Curves, Log-Rank Tests, and Cox Regression for Time-to-Event Data.
- The null hypothesis tested by the log-rank test is that the survival curves are identical over time; it thus compares the entire curves rather than the survival probability at a specific time point.
- The log-rank test assesses statistical significance but does not estimate an effect size.
- The Cox proportional hazards regression5 technique does not actually model the survival time or probability but the so-called hazard function. This function can be thought of as the instantaneous risk of experiencing the event of interest at a certain time point.
- While the HR is not the same as a relative risk, it can for all practical purposes be interpreted as such. See Survival Analysis and Interpretation of Time-to-Event Data: The Tortoise and the Hare.
The logrank test in BMJ, 2004
- The logrank test is based on the same assumptions as the Kaplan Meier survival curve—namely, that censoring is unrelated to prognosis, the survival probabilities are the same for subjects recruited early and late in the study, and the events happened at the times specified. Deviations from these assumptions matter most if they are satisfied differently in the groups being compared, for example if censoring is more likely in one group than another.
- The logrank test is most likely to detect a difference between groups when the risk of an event is consistently greater for one group than another. It is unlikely to detect a difference when survival curves cross, as can happen when comparing a medical with a surgical intervention.
- Statistics review 12: Survival analysis
- 生存分析（三）log-rank检验在什么情况下失效？ Wilcoxon test
Visualize a survival estimate according to a continuous variable.
- Smooth survival plot - quantile of survival
- What would cox regression for continuous covariate looks like? How to interpret it? You could bin the continuous variable into buckets and then look at a Kaplan Meier curve to get an idea of how various levels of the continuous variable impact survival - assuming the variable isn't time-dependent.
- Cox regression themselves does not estimate survival. Cox regression estimates Hazard Ratio.
How to access the fit of a Cox regression?
Read the comment in the section Analyzing Continuous Variables Kaplan Meier Mistakes
- Analyzing Continuous Variables. Optimal cutpoint is problematic because testing every cutpoint creates a multiple testing problem. dichotomization causes loss of statistical power; using binary variables instead of continuous variables can triple the number of samples needed to detect an effect. Dichotomization also makes poor assumptions about the distribution of risk among patients,
- Covariate Adjustment. Kaplan Meier is a univariate method. At a minimum the variable should be analyzed in a Cox model with other basic prognostic factors.
- Added Value. AUC-ROC, the Likelihood Ratio Test, and R² .
An example

R> sdf <- survdiff(Surv(futime, fustat) ~ rx, data = ovarian)
R> sdf$chisq
[1] 1.06274
R> 1 - pchisq(sdf$chisq, length(sdf$n) - 1) 
[1] 0.3025911                                 <----------
R> fit <- coxph(Surv(futime, fustat) ~ rx, data = ovarian)
R> coef(summary(fit))[, "Pr(>|z|)"]
[1] 0.3096304
R> fit$score
[1] 1.06274
R> summary(fit)
Call:
coxph(formula = Surv(futime, fustat) ~ rx, data = ovarian)

  n= 26, number of events= 12 

      coef exp(coef) se(coef)      z Pr(>|z|)
rx -0.5964    0.5508   0.5870 -1.016     0.31

   exp(coef) exp(-coef) lower .95 upper .95
rx    0.5508      1.816    0.1743      1.74

Concordance= 0.608  (se = 0.07 )
Likelihood ratio test= 1.05  on 1 df,   p=0.3
Wald test            = 1.03  on 1 df,   p=0.3
Score (logrank) test = 1.06  on 1 df,   p=0.3  <--- df = model df

Two-sided vs one-sided p-value

The p-value that R (or SAS) returns is for a two-sided test. To obtain a one-sided p-value from this, simply divide the two-sided p-value by 2. Survival Statistics with PROC LIFETEST and PROC PHREG: Pitfall-Avoiding Survival Lessons for Programmers.

> survdiff(Surv(futime, fustat) ~ rx,data=ovarian)
Call:
survdiff(formula = Surv(futime, fustat) ~ rx, data = ovarian)

      N Observed Expected (O-E)^2/E (O-E)^2/V
rx=1 13        7     5.23     0.596      1.06
rx=2 13        5     6.77     0.461      1.06

 Chisq= 1.1  on 1 degrees of freedom, p= 0.3 
> pchisq(1.1, 1, lower.tail = F)
[1] 0.2942661
> pnorm(sqrt(1.1), 0, 1, lower.tail = F)
[1] 0.1471331

Create 2 groups from a continuous variable

See case_when() or tidyverse

merged_data = merged_data %>% 
  mutate(group = case_when(
    KRAS_expression > quantile(KRAS_expression, 0.5) ~ 'KRAS_High',
    KRAS_expression < quantile(KRAS_expression, 0.5) ~ 'KRAS_Low',
    TRUE ~ NA_character_
  ))

fit = survfit(Surv(time, status) ~ group, data = merged_data)

Optimal cut-off

X-Tile: A New Bio-Informatics Tool for Biomarker Assessment and Outcome-Based Cut-Point Optimization .
- Youtube video
- Specifically, a χ2 value is calculated for every possible division of the population shown on the grid using a color code. the program can select the optimal division of the data by selecting the highest χ2 value.
- This is used by Detecting prognostic biomarkers of breast cancer by regularized Cox proportional hazards models Li 2021.
How to determine the cut-point of continuous predictor in survival analysis, optimal or median cut-point?
- ...usually the variable itself or some continuous transformation of it will be more useful in an outcome model.
- Are the costs of placing a low-risk case into the high-risk category really the same as the opposite type of error?

Survival curve with confidence interval

http://www.sthda.com/english/wiki/survminer-r-package-survival-data-analysis-and-visualization

Parametric models and survival function for censored data

Assume the CDF of survival time T is [math]\displaystyle{ F(\cdot) }[/math] and the CDF of the censoring time C is [math]\displaystyle{ G(\cdot) }[/math],

[math]\displaystyle{ \begin{align} P(T\gt t, \delta=1) &= \int_t^\infty (1-G(s))dF(s), \\ P(T\gt t, \delta=0) &= \int_t^\infty (1-F(s))dG(s) \end{align} }[/math]

http://www.stat.columbia.edu/~madigan/W2025/notes/survival.pdf#page=23
http://www.ms.uky.edu/~mai/sta635/LikelihoodCensor635.pdf#page=2 survival function of [math]\displaystyle{ f(T, \delta) }[/math]
https://web.stanford.edu/~lutian/coursepdf/unit2.pdf#page=3 joint density of [math]\displaystyle{ f(T, \delta) }[/math]
http://data.princeton.edu/wws509/notes/c7.pdf#page=6
Special case: T follows Log normal distribution and C follows [math]\displaystyle{ U(0, \xi) }[/math].

R

flexsurv package.
Parametric survival modeling which uses the flexsurv package.
Used in simsurv package

Parametric models and likelihood function for uncensored data

plot.survfit()

Exponential. [math]\displaystyle{ T \sim Exp(\lambda) }[/math]. [math]\displaystyle{ H(t) = \lambda t. }[/math] and [math]\displaystyle{ ln(S(t)) = -H(t) = -\lambda t. }[/math]
Weibull. [math]\displaystyle{ T \sim W(\lambda,p). }[/math] [math]\displaystyle{ H(t) = \lambda^p t^p. }[/math] and [math]\displaystyle{ ln(-ln(S(t))) = ln(\lambda^p t^p)=const + p ln(t) }[/math].

http://www.math.ucsd.edu/~rxu/math284/slect4.pdf

See also accelerated life models where a set of covariates were used to model survival time.

log-normal model
- Comparing of Cox model and parametric models in analysis of effective factors on event time of neuropathy in patients with type 2 diabetes. According to AIC, log-normal model with the lowest Akaike's was the best-fitted model among Cox and parametric models.
- Generating/plotting a log-normal survival function
- Log Normal Distribution in R (4 Examples) | dlnorm, plnorm, qlnorm & rlnorm Functions
- Parametric survival modeling

Survival modeling

Accelerated life models - a direct extension of the classical linear model

http://data.princeton.edu/wws509/notes/c7.pdf and also Kalbfleish and Prentice (1980).

[math]\displaystyle{ log T_i = x_i' \beta + \epsilon_i }[/math] Therefore

[math]\displaystyle{ T_i = exp(x_i' \beta) T_{0i} }[/math]. So if there are two groups (x=1 and x=0), and [math]\displaystyle{ exp(\beta) = 2 }[/math], it means one group live twice as long as people in another group.
[math]\displaystyle{ S_1(t) = S_0(t/ exp(x' \beta)) }[/math]. This explains the meaning of accelerated failure-time. Depending on the sign of [math]\displaystyle{ \beta' x }[/math], the time is either accelerated by a constant factor or degraded by a constant factor. If [math]\displaystyle{ exp(\beta)=2 }[/math], the probability that a member in group one (eg treatment) will be alive at age t is exactly the same as the probability that a member in group zero (eg control group) will be alive at age t/2.
The hazard function [math]\displaystyle{ \lambda_1(t) = \lambda_0(t/exp(x'\beta))/ exp(x'\beta) }[/math]. So if [math]\displaystyle{ exp(\beta)=2 }[/math], at any given age people in group one would be exposed to half the risk of people in group zero half their age.

In applications,

If the errors are normally distributed, then we obtain a log-normal model for the T. Estimation of this model for censored data by maximum likelihood is known in the econometric literature as a Tobit model.
If the errors have an extreme value distribution, then T has an exponential distribution. The hazard [math]\displaystyle{ \lambda }[/math] satisfies the log linear model [math]\displaystyle{ \log \lambda_i = x_i' \beta }[/math].

Proportional hazard models

Note PH models is a type of multiplicative hazard rate models [math]\displaystyle{ h(x|Z) = h_0(x)c(\beta' Z) }[/math] where [math]\displaystyle{ c(\beta' Z) = \exp(\beta ' Z) }[/math].

Assumption: Survival curves for two strata (determined by the particular choices of values for covariates) must have hazard functions that are proportional over time (i.e. constant relative hazard over time). Proportional hazards assumption meaning. The ratio of the hazard rates from two individuals with covariate value [math]\displaystyle{ Z }[/math] and [math]\displaystyle{ Z^* }[/math] is a constant function time.

[math]\displaystyle{ \begin{align} \frac{h(t|Z)}{h(t|Z^*)} = \frac{h_0(t)\exp(\beta 'Z)}{h_0(t)\exp(\beta ' Z^*)} = \exp(\beta' (Z-Z^*)) \mbox{ independent of time} \end{align} }[/math]

Test the assumption; see here.

Weibull and Exponential model to Cox model

https://socserv.socsci.mcmaster.ca/jfox/Books/Companion/appendix/Appendix-Cox-Regression.pdf. It also includes model diagnostic and all stuff is illustrated in R.
http://stat.ethz.ch/education/semesters/ss2011/seminar/contents/handout_9.pdf

In summary:

Weibull distribution (Klein) [math]\displaystyle{ h(t) = p \lambda (\lambda t)^{p-1} }[/math] and [math]\displaystyle{ S(t) = exp(-\lambda t^p) }[/math]. If p >1, then the risk increases over time. If p<1, then the risk decreases over time.
- Note that Weibull distribution has a different parametrization. See http://data.princeton.edu/pop509/ParametricSurvival.pdf#page=2. [math]\displaystyle{ h(t) = \lambda^p p t^{p-1} }[/math] and [math]\displaystyle{ S(t) = exp(-(\lambda t)^p) }[/math]. R and wikipedia also follows this parametrization except that [math]\displaystyle{ h(t) = p t^{p-1}/\lambda^p }[/math] and [math]\displaystyle{ S(t) = exp(-(t/\lambda)^p) }[/math].
Exponential distribution [math]\displaystyle{ h(t) }[/math] = constant (independent of t). This is a special case of Weibull distribution (p=1).
Weibull (and also exponential) ~~distribution~~ regression model is the only case which belongs to both the proportional hazards and the accelerated life families.

[math]\displaystyle{ \begin{align} \frac{h(x|Z_1)}{h(x|Z_2)} = \frac{h_0(x\exp(-\gamma' Z_1)) \exp(-\gamma ' Z_1)}{h_0(x\exp(-\gamma' Z_2)) \exp(-\gamma ' Z_2)} = \frac{(a/b)\left(\frac{x \exp(-\gamma ' Z_1)}{b}\right)^{a-1}\exp(-\gamma ' Z_1)}{(a/b)\left(\frac{x \exp(-\gamma ' Z_2)}{b}\right)^{a-1}\exp(-\gamma ' Z_2)} \quad \mbox{which is independent of time x} \end{align} }[/math]

Using the Weibull baseline hazard is the only circumstance under which the model satisfies both the proportional hazards, and accelerated failure time models
If X is exponential distribution with mean [math]\displaystyle{ b }[/math], then X^(1/a) follows Weibull(a, b). See Exponential distribution and Weibull distribution.
Derivation of mean and variance of Weibull distribution.

	f(t)=h(t)*S(t)	h(t)	S(t)	Mean
Exponential (Klein p37)	[math]\displaystyle{ \lambda \exp(-\lambda t) }[/math]	[math]\displaystyle{ \lambda }[/math]	[math]\displaystyle{ \exp(-\lambda t) }[/math]	[math]\displaystyle{ 1/\lambda }[/math]
Weibull (Klein, Bender, wikipedia)	[math]\displaystyle{ p\lambda t^{p-1}\exp(-\lambda t^p) }[/math]	[math]\displaystyle{ p\lambda t^{p-1} }[/math]	[math]\displaystyle{ exp(-\lambda t^p) }[/math]	[math]\displaystyle{ \frac{\Gamma(1+1/p)}{\lambda^{1/p}} }[/math]
Exponential (R)	[math]\displaystyle{ \lambda \exp(-\lambda t) }[/math], [math]\displaystyle{ \lambda }[/math] is rate	[math]\displaystyle{ \lambda }[/math]	[math]\displaystyle{ \exp(-\lambda t) }[/math]	[math]\displaystyle{ 1/\lambda }[/math]
Weibull (R, wikipedia)	[math]\displaystyle{ \frac{a}{b}\left(\frac{t}{b}\right)^{a-1} \exp(-(\frac{t}{b})^a) }[/math], [math]\displaystyle{ a }[/math] is shape, and [math]\displaystyle{ b }[/math] is scale	[math]\displaystyle{ \frac{a}{b}\left(\frac{t}{b}\right)^{a-1} }[/math]	[math]\displaystyle{ \exp(-(\frac{t}{b})^a) }[/math]	[math]\displaystyle{ b\Gamma(1+1/a) }[/math]

Accelerated failure-time model. Let [math]\displaystyle{ Y=\log(T)=\mu + \gamma'Z + \sigma W }[/math]. Then the survival function of [math]\displaystyle{ T }[/math] at the covariate Z,

[math]\displaystyle{ \begin{align} S_T(t|Z) &= P(T \gt t |Z) \\ &= P(Y \gt \ln t|Z) \\ &= P(\mu + \sigma W \gt \ln t-\gamma' Z | Z) \\ &= P(e^{\mu + \sigma W} \gt t\exp(-\gamma'Z) | Z) \\ &= S_0(t \exp(-\gamma'Z)). \end{align} }[/math]

where [math]\displaystyle{ S_0(t) }[/math] denote the survival function T when Z=0. Since [math]\displaystyle{ h(t) = -\partial \ln (S(t)) }[/math], the hazard function of T with a covariate value Z is related to a baseline hazard rate [math]\displaystyle{ h_0 }[/math] by (p56 Klein)

[math]\displaystyle{ \begin{align} h(t|Z) = h_0(t\exp(-\gamma' Z)) \exp(-\gamma ' Z) \end{align} }[/math]

> mean(rexp(1000)^(1/2))
[1] 0.8902948
> mean(rweibull(1000, 2, 1))
[1] 0.8856265

> mean((rweibull(1000, 2, scale=4)/4)^2)
[1] 1.008923

Graphical way to check Weibull, AFT, PH

http://stat.ethz.ch/education/semesters/ss2011/seminar/contents/handout_9.pdf#page=40

Weibull is related to Extreme value distribution

Log(Weibull) = Extreme value
Extreme Value Distributions from mathwave.com
Generalized extreme value distribution from wikipedia
Density, distribution function, quantile function, and random generation for the (largest) extreme value distribution from EnvStats R package
Lesson 60 – Extreme value distributions in R

Weibull distribution and bathtub

Weibull distribution and reliability

Survival Analysis – Fitting Weibull Models for Improving Device Reliability in R (simulation)

Optimisation of a Weibull survival model using Optimx()

Optimisation of a Weibull survival model using Optimx() in R

CDF follows Unif(0,1)

https://stats.stackexchange.com/questions/161635/why-is-the-cdf-of-a-sample-uniformly-distributed

Take the Exponential distribution for example

stem(pexp(rexp(1000)))
stem(pexp(rexp(10000)))

Another example is from simulating survival time. Note that this is exactly Bender et al 2005 approach. See also the simsurv (newer) and survsim (older) packages.

set.seed(100) 

#Define the following parameters outlined in the step: 
n = 1000 
beta_0 = 0.5
beta_1 = -1
beta_2 = 1 

b = 1.6 #This will be changed later as mentioned in Step 5 of documentation 

#Step 1
x_1<-rbinom(n, 1, 0.25)
x_2<-rbinom(n, 1, 0.7)

#Step 2 
U<-runif(n, 0,1)
T<-(-log(U)*exp(-(beta_0+beta_1*x_1+beta_2*x_2))) #Eqn (5) 

Fn <- ecdf(T) # https://stat.ethz.ch/R-manual/R-devel/library/stats/html/ecdf.html
# verify F(T) or 1-F(T) ~ U(0, 1)
hist(Fn(T))
# look at the plot of survival probability vs time
plot(T, 1 - Fn(T))

Simulate survival data

Note that status = 1 means an event (e.g. death) happened; Ti <= Ci. That is, the status variable used in R/Splus means the death indicator.

http://www.bioconductor.org/packages/release/bioc/manuals/genefilter/man/genefilter.pdf#page=4
```
y <- rexp(10)
cen <- runif(10)
status <- ifelse(cen < .7, 1, 0)
```
Inference on Selected Subgroups in Clinical Trials [math]\displaystyle{ \lambda(t) = \lambda_0(t) e^{\beta_i D} }[/math] for subgroup i=1,2, respectively where D is the treatment indicator and [math]\displaystyle{ \lambda_0(t) }[/math] is the baseline hazard function of Weibull(1,1). The subjects fall into one of the two subgroups with probability 0.5, and the treatment assignment is also random with equal probability. The response generated from the above model is then censored randomly from the right by a censoring variable C, where log(C) follows the uniform distribution on (-1.25, 1.00). The censoring rate is about 40% across different choices of [math]\displaystyle{ \beta_i }[/math] considered in this study.

How much power/accuracy is lost by using the Cox model instead of Weibull model when both model are correct? [math]\displaystyle{ h(t|x)=\lambda=e^{3x+1} = h_0(t)e^{\beta x} }[/math] where [math]\displaystyle{ h_0(t)=e^1, \beta=3 }[/math].

Note that for the exponential distribution, larger rate/[math]\displaystyle{ \lambda }[/math] corresponds to a smaller mean. This relation matches with the Cox regression where a large covariate corresponds to a smaller survival time. So the coefficient 3 in myrates in the below example has the same sign as the coefficient (2.457466 for censored data) in the output of the Cox model fitting.

n <- 30
x <- scale(1:n, TRUE, TRUE) # create covariates (standardized)
                            # the original example does not work on large 'n'
myrates <- exp(3*x+1)
set.seed(1234)
y <- rexp(n, rate = myrates) # generates the r.v.
cen <- rexp(n, rate = 0.5 )  #  E(cen)=1/rate
ycen <- pmin(y, cen)
di <- as.numeric(y <= cen)
survreg(Surv(ycen, di)~x, dist="weibull")$coef[2]  # -3.080125
# library(flexsurvreg); flexsurvreg(Surv(ycen, di)~x, dist="weibull")
coxph(Surv(ycen, di)~x)$coef  # 2.457466 

# no censor
survreg(Surv(y,rep(1, n))~x,dist="weibull")$coef[2]  # -3.137603
survreg(Surv(y,rep(1, n))~x,dist="exponential")$coef[2]  # -3.143095
coxph(Surv(y,rep(1, n))~x)$coef  # 2.717794 

# See the pdf note for the rest of code

Intercept in survreg for the exponential distribution. http://www.stat.columbia.edu/~madigan/W2025/notes/survival.pdf#page=25.
[math]\displaystyle{ \begin{align} \lambda = exp(-intercept) \end{align} }[/math]
```
> futime <- rexp(1000, 5)
> survreg(Surv(futime,rep(1,1000))~1,dist="exponential")$coef
(Intercept) 
  -1.618263 
> exp(1.618263)
[1] 5.044321
```

Intercept and scale in survreg for a Weibull distribution. http://www.stat.columbia.edu/~madigan/W2025/notes/survival.pdf#page=28.

[math]\displaystyle{ \begin{align} \gamma &= 1/scale \\ \alpha &= exp(-(Intercept)*\gamma) \end{align} }[/math]

> survreg(Surv(futime,rep(1,1000))~1,dist="weibull")
Call:
survreg(formula = Surv(futime, rep(1, 1000)) ~ 1, dist = "weibull")

Coefficients:
(Intercept) 
  -1.639469 

Scale= 1.048049 

Loglik(model)= 620.1   Loglik(intercept only)= 620.1
n= 1000

rsurv() function from the ipred package
Use Weibull distribution to model survival data. We assume the shape is constant across subjects. We then allow the scale to vary across subjects. For subject [math]\displaystyle{ i }[/math] with covariate [math]\displaystyle{ X_i }[/math], [math]\displaystyle{ \log(scale_i) }[/math] = [math]\displaystyle{ \beta ' X_i }[/math]. Note that if we want to make the [math]\displaystyle{ \beta }[/math] sign to be consistent with the Cox model, we want to use [math]\displaystyle{ \log(scale_i) }[/math] = [math]\displaystyle{ -\beta ' X_i }[/math] instead.

http://sas-and-r.blogspot.com/2010/03/example-730-simulate-censored-survival.html. Assuming shape=1 in the Weibull distribution, then the hazard function can be expressed as a proportional hazard model

[math]\displaystyle{ h(t|x) = 1/scale = \frac{1}{\lambda/e^{\beta 'x}} = \frac{e^{\beta ' x}}{\lambda} = h_0(t) \exp(\beta' x) }[/math]

n = 10000
beta1 = 2; beta2 = -1
lambdaT = .002 # baseline hazard
lambdaC = .004  # hazard of censoring
set.seed(1234)
x1 = rnorm(n,0)
x2 = rnorm(n,0)
# true event time
T = Vectorize(rweibull)(n=1, shape=1, scale=lambdaT*exp(-beta1*x1-beta2*x2)) 
# No censoring
event2 <- rep(1, length(T))
coxph(Surv(T, event2)~ x1 + x2)
#        coef exp(coef) se(coef)      z      p
# x1  1.99825   7.37613  0.01884 106.07 <2e-16
# x2 -1.00200   0.36715  0.01267 -79.08 <2e-16
#
# Likelihood ratio test=15556  on 2 df, p=< 2.2e-16
# n= 10000, number of events= 10000 

# Censoring
C = rweibull(n, shape=1, scale=lambdaC)   #censoring time
time = pmin(T,C)  #observed time is min of censored and true
event = time==T   # set to 1 if event is observed
coxph(Surv(time, event)~ x1 + x2)
#        coef exp(coef) se(coef)      z      p
# x1  2.01039   7.46622  0.02250  89.33 <2e-16
# x2 -0.99210   0.37080  0.01552 -63.95 <2e-16
#
# Likelihood ratio test=11321  on 2 df, p=< 2.2e-16
# n= 10000, number of events= 6002
mean(event)
# [1] 0.6002

https://stats.stackexchange.com/a/135129 (Bender's inverse probability method). Let [math]\displaystyle{ h_0(t)=\lambda \rho t^{\rho - 1} }[/math] where shape 𝜌>0 and scale 𝜆>0. Following the inverse probability method, a realisation of 𝑇∼𝑆(⋅|𝐱) is obtained by computing [math]\displaystyle{ t = \left( - \frac{\log(v)}{\lambda \exp(x' \beta)} \right) ^ {1/\rho} }[/math] with 𝑣 a uniform variate on (0,1). Using results on transformations of random variables, one may notice that 𝑇 has a conditional Weibull distribution (given 𝐱) with shape 𝜌 and scale 𝜆exp(𝐱′𝛽).

# N = sample size    
# lambda = scale parameter in h0()
# rho = shape parameter in h0()
# beta = fixed effect parameter
# rateC = rate parameter of the exponential distribution of censoring variable C

simulWeib <- function(N, lambda, rho, beta, rateC)
{
  # covariate --> N Bernoulli trials
  x <- sample(x=c(0, 1), size=N, replace=TRUE, prob=c(0.5, 0.5))

  # Weibull latent event times
  v <- runif(n=N)
  Tlat <- (- log(v) / (lambda * exp(x * beta)))^(1 / rho)

  # censoring times
  C <- rexp(n=N, rate=rateC)

  # follow-up times and event indicators
  time <- pmin(Tlat, C)
  status <- as.numeric(Tlat <= C)

  # data set
  data.frame(id=1:N,
             time=time,
             status=status,
             x=x)
}
# Test
set.seed(1234)
betaHat <- rate <- rep(NA, 1e3)
for(k in 1:1e3)
{
  dat <- simulWeib(N=100, lambda=0.01, rho=1, beta=-0.6, rateC=0.001)
  fit <- coxph(Surv(time, status) ~ x, data=dat)
  rate[k] <- mean(dat$status == 0)
  betaHat[k] <- fit$coef
}
mean(rate)
# [1] 0.12287
mean(betaHat)
# [1] -0.6085473

Generating survival times to simulate Cox proportional hazards models Bender et al 2005 [math]\displaystyle{ T=H_0^{-1}[-\log(U) \exp(\beta' x)] }[/math] Bender2005.png, Bender2005table2.png
- survsim package and the paper on JSS. See this post. Biologically Plausible Fake Survival Data
- simsurv package (new, 2 vignettes).
- Get a desired percentage of censored observations in a simulation of Cox PH Model. The answer is based on Bender et al 2005. Generating survival times to simulate Cox proportional hazards models. Statistics in Medicine 24: 1713–1723. The censoring time is fixed and the distribution of the censoring indicator is following the binomial. In fact, when we simulate survival data with a predefined censoring rate, we can pretend the survival time is already censored and only care about the censoring/status variable to make sure the censoring rate is controlled.
- (Search github) Using inverse CDF [math]\displaystyle{ \lambda = exp(\beta' x), \; S(t)= \exp(-\lambda t) = \exp(-t e^{\beta' x}) \sim Unif(0,1) }[/math]
- Prediction Accuracy Measures for a Nonlinear Model and for Right-Censored Time-to-Event Data Li and Wang

Simple example from glmnet

set.seed(10101)
N = 1000
p = 30
nzc = p/3
x = matrix(rnorm(N * p), N, p)
beta = rnorm(nzc)
fx = x[, seq(nzc)] %*% beta/3
hx = exp(fx)
ty = rexp(N, hx)
tcens = rbinom(n = N, prob = 0.3, size = 1)  # censoring indicator
y = cbind(time = ty, status = 1 - tcens)  # y=Surv(ty,1-tcens) with library(survival)
fit = glmnet(x, y, family = "cox")
pred = predict(fit, newx = x)
Cindex(pred, y)

A non-standard baseline hazard function [math]\displaystyle{ \lambda_0(t)=(t - .5)^2 }[/math] from the paper: A new nonparametric screening method for ultrahigh-dimensional survival data Liu 2018. The censoring time [math]\displaystyle{ C = \widetilde{C} \wedge \tau }[/math], where [math]\displaystyle{ \widetilde{C} }[/math] was generated from Unif (0, [math]\displaystyle{ \tau + 2 }[/math]) where [math]\displaystyle{ \tau }[/math] was chosen to yield the desirable censoring rates of 20% and 40%, respectively.
Regularization paths for Cox's proportional hazards model via coordinate descent. J Stat Software Simon et al 2011. Gsslasso Cox: a Bayesian hierarchical model for predicting survival and detecting associated genes by incorporating pathway information by Tang 2019. See also Tian 2014 JASA p1525. X ~ standard Gaussian. True survival time exp(beta X + k · Z). Z ~ N(0,1), and k is chosen so that the signal-to-noise ratio is 3.0 or to induce a certain censoring rate. Censoring time C = exp (k · Z). The observed survival time T = min{Y, C}.
survParamSim: Parametric Survival Simulation with Parameter Uncertainty
vivaGen – a survival data set generator for software testing BMC Bioinformatics 2020
Simulating survival outcomes: setting the parameters for the desired distribution. simstudy, Follow-up: simstudy function for generating parameters for survival distribution package was used.

Warning on multiple rates

Search Vectorize() function in this page.

mean(rexp(1000, rate=2) )
# [1] 0.5258078
mean(rexp(1000, rate=1) )
# [1] 0.9712124

z = rexp(1000, rate=c(1, 2))
mean(z[seq(1, 1000, by=2)])
# [1] 1.041969
mean(z[seq(2, 1000, by=2)])
# [1] 0.5079594

Markov model

Fake Survival Data for the Disease Progression Model

Non-proportional hazards

Simulating time-to-event outcomes with non-proportional hazards

Standardize covariates

coxph() does not have an option to standardize covariates but glmnet() does.

library(glmnet)
library(survival)

N=1000;p=30
nzc=p/3
beta <- c(rep(1, 5), rep(-1, 5))

set.seed(1234)
  x=matrix(rnorm(N*p),N,p)
  x[, 1:5] <- x[, 1:5]*2
  x[, 6:10] <- x[, 6:10] + 2

  fx=x[,seq(nzc)] %*% beta
  hx=exp(fx)
  ty=rexp(N,hx)
  tcens <- rep(0,N)
  y=cbind(time=ty,status=1-tcens) # y=Surv(ty,1-tcens) with library(survival)

coxph(Surv(ty, 1-tcens) ~ x) %>% coef %>% head(10)
#         x1         x2         x3         x4         x5         x6         x7
#  0.6076146  0.6359927  0.6346022  0.6469274  0.6152082 -0.6614930 -0.5946101
#         x8         x9        x10
# -0.6726081 -0.6275205 -0.7073704

xscale <- scale(x, TRUE, TRUE) # halve the covariate values
coxph(Surv(ty, 1-tcens) ~ xscale) %>% coef %>% head(10) # double the coef
#    xscale1    xscale2    xscale3    xscale4    xscale5    xscale6    xscale7
#  1.2119940  1.2480628  1.2848646  1.2857796  1.1959619 -0.6431946 -0.5941309
#    xscale8    xscale9   xscale10
# -0.6723137 -0.6188384 -0.6793313

  set.seed(1)
  fit=cv.glmnet(x,y,family="cox", nfolds=10, standardize = TRUE)
  as.vector(coef(fit, s = "lambda.min"))[seq(nzc)]
# [1]  0.9351341  0.9394696  0.9187242  0.9418540  0.9111623 -0.9303783
# [7] -0.9271438 -0.9597583 -0.9493759 -0.9386065

  set.seed(1)
  fit=cv.glmnet(x,y,family="cox", nfolds=10, standardize = FALSE)
  as.vector(coef(fit, s = "lambda.min"))[seq(nzc)]
# [1]  0.9357171  0.9396877  0.9200247  0.9420215  0.9118803 -0.9257406
# [7] -0.9232813 -0.9554017 -0.9448827 -0.9356009  

  set.seed(1)
  fit=cv.glmnet(xscale,y,family="cox", nfolds=10, standardize = TRUE)
  as.vector(coef(fit, s = "lambda.min"))[seq(nzc)]
# [1]  1.8652889  1.8436015  1.8601198  1.8719515  1.7712951 -0.9046420
# [7] -0.9263966 -0.9593383 -0.9362407 -0.9014015

  set.seed(1)
  fit=cv.glmnet(xscale,y,family="cox", nfolds=10, standardize = FALSE)
  as.vector(coef(fit, s = "lambda.min"))[seq(nzc)]
# [1]  1.8652889  1.8436015  1.8601198  1.8719515  1.7712951 -0.9046420
# [7] -0.9263966 -0.9593383 -0.9362407 -0.9014015

Predefined censoring rates

Simulating survival data with predefined censoring rates for proportional hazards models

Cross validation

Cross validation in survival analysis by Verweij & van Houwelingen, Stat in medicine 1993.
Cross- Validated Cox Regression on Microarray Gene Expression Data van Houwelingen HC, Bruinsma T, Hart AAM, van’t Veer LJ, Wessels LFA (2006). Statistics in Medicine, 25, 3201–3216
Using cross-validation to evaluate predictive accuracy of survival risk classifiers based on high-dimensional data. Simon et al, Brief Bioinform. 2011
- Testing the additional predictive value of high-dimensional molecular data. the cross-validated probabilities are not independent from each other.
- A study of pre-validation. Annals of Applied Statistics. 2008

CVPL (cross-validated partial likelihood)
- https://www.rdocumentation.org/packages/survcomp/versions/1.22.0/topics/cvpl (lower is better)
- https://rdrr.io/cran/dynpred/man/CVPL.html. source code. 1. it does LOOCV so no need to set a random seed. 2. it seems the function does not include lasso/glmnet 3. the formula on pages 173-174 of the book Dynamic Prediction in Clinical Survival Analysis says the partial log likelihood should include the penalty term. 4. concordance measures like Harrell’s C-index are not appropriate because they only measure the discrimination and not the calibration. PS: I downloaded and looked at the chapter source code. It uses optL1() function from the penalized package to obtain cross validated log partial likelihood.
```
R> library(dynpred)
R> data(ova)
R> CVPL(Surv(tyears, d) ~ 1, data = ova)
[1] NA
R> CVPL(Surv(tyears, d) ~ Karn + Broders + FIGO + Ascites + Diam,
   data = ova)
[1] -1652.169
R> coxph(Surv(tyears, d) ~ Karn + Broders + FIGO + Ascites + Diam, data = ova)$loglik[2] # No CV
[1] -1374.717
```
- optL1() from the penalized package. It seems the penalized package has its own sequence of lambdas and these lambdas are totally different from glmnet() has created though the CV plot from each package shows a convex shape.
- Gsslasso paper. CVPL does not include the penalty term.
- https://web.stanford.edu/~hastie/Papers/v39i05.pdf#page=10 (larger is better)

Competing risk and cumulative incidence

https://www.mailman.columbia.edu/research/population-health-methods/competing-risk-analysis. Subjects can potentially experience more than one type of a certain event. For instance, if mortality is of research interest, then our observations – senior patients at an oncology department, could possibly die from heart attack or breast cancer, or even traffic accident. When only one of these different types of event can occur, we refer to these events as “competing events”, in a sense that they compete with each other to deliver the event of interest, and the occurrence of one type of event will prevent the occurrence of the others.
Page 61 of Klein and Moeschberger "Survival Analysis"
Survival Analysis in R Emily Zabor
10.9 Competing risks regression from the ebook R for Health Data Science.
Competing risk analysis using R: an easy guide for clinicians 2007
Regression modeling of competing risk using R: an in depth guide for clinicians 2010

Survival rate terminology

How is the overall survival measured?
- The length of time from either the date of diagnosis or the start of treatment for a disease, such as cancer, that patients diagnosed with the disease are still alive. In a clinical trial, measuring the overall survival is one way to see how well a new treatment works. NCI Dictionary of Cancer Terms
- Overall survival, or OS, or sometimes just “survival” is the percentage of people in a group who are alive after a length of time—usually a number of years.
How is progression-free survival measured?
- The length of time during and after the treatment of a disease, such as cancer, that a patient lives with the disease but it does not get worse. In a clinical trial, measuring the progression-free survival is one way to see how well a new treatment works. NCI Dictionary of Cancer Terms
- Progression-free survival (PFS) was measured as the interval between the initiation of treatment until either disease recurrence or last documented follow-up of the patient if he/she remains disease-free.
OS vs PFS
- Understanding the endpoints in oncology: overall survival, progression free survival, hazard ratio, censored value
- Relationship between Progression-free Survival and Overall Survival in Randomized Clinical Trials of Targeted and Biologic Agents in Oncology

Progression-free survival (PFS), overall survival (OS).
- PFS is the length of time during and after the treatment of a disease, such as cancer, that a patient lives with the disease but it does not get worse. See an use at NCI-MATCH trial.

Disease-free survival (DFS): the period after curative treatment [disease eliminated] when no disease can be detected
- DFS stands for disease-free survival, which measures the length of time that a patient survives without any signs or symptoms of the disease or cancer recurrence. It is calculated from the date of treatment initiation to the date of disease recurrence or death from any cause. DFS is often used as a secondary endpoint in clinical trials, especially in early-stage cancers where the primary goal of treatment is to achieve long-term remission.
- What Is The Difference Between PFS And DFS? Disease-free survival (DFS), also known as relapse-free survival (RFS), is often used as the primary endpoint in phase III trials of adjuvant therapy. Progression-free survival (PFS) is commonly used as the primary endpoint in phase III trials evaluating the treatment of metastatic cancer.
- The main difference between PFS and DFS is that PFS measures the time until the cancer progresses, whereas DFS measures the time until the cancer recurs or returns after treatment. PFS is generally considered a more sensitive measure of treatment efficacy than DFS because it accounts for any disease progression, not just a recurrence. However, DFS may be more appropriate for patients with early-stage cancer who are at lower risk of disease progression but have a higher risk of disease recurrence.

Time to progression: The length of time from the date of diagnosis or the start of treatment for a disease until the disease starts to get worse or spread to other parts of the body. In a clinical trial, measuring the time to progression is one way to see how well a new treatment works. Also called TTP.
Metastasis-free survival (MFS) time: the period until metastasis is detected
Event free survival (EFS)
Understanding Statistics Used to Guide Prognosis and Evaluate Treatment (DFS & PFS rate)
Distant recurrence means the cancer has come back in another part of the body, Three types of recurrence?, NCI dictionaries
Are the disease-free survival (DFS) and recurrence-free survival (RFS) the same definitions in oncology studies?. Yes.
What is the difference between overall survival (OS), recurrence-free survival (RFS) and time-to-recurrence?
Recurrence-free survival (RFS) vs progression-free survival (PFS)
- Recurrence-Free: This term is used when cancer has been eliminated or reduced to an undetectable level, and then returns after a period of time. Typically starts at a specific point such as the date of diagnosis or the end of treatment. The end time is usually the date of disease recurrence or the end of the follow-up period.
- Progression-Free: This term is used to describe the period of time during and after treatment when the disease does not get worse. It’s often used in situations where a tumor is present, as demonstrated by laboratory testing, radiologic testing, or clinically. Start Time is usually the time point when a patient starts their treatment. It could also be the date of diagnosis or randomization. End Time is the time point when disease progression is detected or death occurs. If neither of these events occur, then the end time might be the last follow-up visit or contact with the patient.
redictors of Recurrence, and Progression-Free and Overall Survival following Open versus Robotic Radical Cystectomy: Analysis from the RAZOR Trial with a 3-Year Followup

Time-dependent covariates

Using Time Dependent Covariates and Time Dependent Coefficients in the Cox Mode
Building an Elastic-Net Cox Model with Time-Dependent covariates
Survival Analysis in R Emily Zabor
Difference of Time-dependent covariate and time-independent covariate: The difference between time-dependent and time-independent covariates in the context of a Cox model is indeed in how the Surv() function is used.
```
# Time-independent covariate 
Surv(time, status)

# Time-dependent covariate 
Surv(start, stop, status)
```
Here, start and stop define an interval of time during which the covariates are assumed to be constant. This allows the covariates to change over time, as each subject can have multiple rows in the data corresponding to different time intervals.
Example: Let’s say we’re studying the effect of a treatment on survival time in patients with a certain disease. We have a covariate that changes over time: the dosage of the treatment, which can be increased or decreased at different times for each patient. Our data might look something like this:

Patient ID Start Time Stop Time Status Dosage

1 0 3 0 10

1 3 6 1 20

2 0 2 0 10

2 2 5 0 15

2 5 8 1 15

Here, each row represents a time interval for a patient. The Start Time and Stop Time columns represent the beginning and end of the interval. The Status column indicates whether the event of interest (e.g., death) occurred at the end of the interval (1 if the event occurred, 0 otherwise). The Dosage column is our time-dependent covariate.
A time-dependent covariate in a Cox model becomes a time-independent covariate under the special case where the covariate does not change over the duration of the study for any subject. In other words, if the value of the covariate is constant for each individual across all time points, it can be treated as a time-independent covariate. For example, consider a study investigating the effect of gender (a binary variable: male or female) on survival time. Since an individual’s gender does not change over time, it is a time-independent covariate. On the other hand, a variable like blood pressure, which can change at different time points for the same individual, would typically be considered a time-dependent covariate.

Books

Survival Analysis, A Self-Learning Text by Kleinbaum, David G., Klein, Mitchel
Applied Survival Analysis Using R by Moore, Dirk F.
Regression Modeling Strategies by Harrell, Frank
Regression Methods in Biostatistics by Vittinghoff, E., Glidden, D.V., Shiboski, S.C., McCulloch, C.E.
https://tbrieder.org/epidata/course_reading/e_tableman.pdf
Survival Analysis: Models and Applications by Xian Liu
(online) Survival Analysis in R Michael Foley. survminer ::ggsurvplot(). Landmark analysis. Time-Dependent Covariates.

Class notes

Cox proportional hazards model and the partial log-likelihood function

Let Y_i denote the observed time (either censoring time or event time) for subject i, and let C_i be the indicator that the time corresponds to an event (i.e. if C_i = 1 the event occurred and if C_i = 0 the time is a censoring time). The hazard function for the Cox proportional hazard model has the form

[math]\displaystyle{ \lambda(t|X) = \lambda_0(t)\exp(\beta_1X_1 + \cdots + \beta_pX_p) = \lambda_0(t)\exp(X \beta^\prime). }[/math]

This expression gives the hazard at time t for an individual with covariate vector (explanatory variables) X. Based on this hazard function, a partial likelihood (defined on hazard function) can be constructed from the datasets as

[math]\displaystyle{ L(\beta) = \prod\limits_{i:C_i=1}\frac{\theta_i}{\sum_{j:Y_j\ge Y_i}\theta_j}, }[/math]

where θ_j = exp(X_jβ^′) and X₁, ..., X_n are the covariate vectors for the n independently sampled individuals in the dataset (treated here as column vectors). This pdf or this note give a toy example

The corresponding log partial likelihood is

[math]\displaystyle{ \ell(\beta) = \sum_{i:C_i=1} \left(X_i \beta^\prime - \log \sum_{j:Y_j\ge Y_i}\theta_j\right). }[/math]

This function can be maximized over β to produce maximum partial likelihood estimates of the model parameters.

The partial score function is [math]\displaystyle{ \ell^\prime(\beta) = \sum_{i:C_i=1} \left(X_i - \frac{\sum_{j:Y_j\ge Y_i}\theta_jX_j}{\sum_{j:Y_j\ge Y_i}\theta_j}\right), }[/math]

and the Hessian matrix of the partial log likelihood is

[math]\displaystyle{ \ell^{\prime\prime}(\beta) = -\sum_{i:C_i=1} \left(\frac{\sum_{j:Y_j\ge Y_i}\theta_jX_jX_j^\prime}{\sum_{j:Y_j\ge Y_i}\theta_j} - \frac{\sum_{j:Y_j\ge Y_i}\theta_jX_j\times \sum_{j:Y_j\ge Y_i}\theta_jX_j^\prime}{[\sum_{j:Y_j\ge Y_i}\theta_j]^2}\right). }[/math]

Using this score function and Hessian matrix, the partial likelihood can be maximized using the Newton-Raphson algorithm. The inverse of the Hessian matrix, evaluated at the estimate of β, can be used as an approximate variance-covariance matrix for the estimate, and used to produce approximate standard errors for the regression coefficients.

If X is age, then the coefficient is likely >0. If X is some treatment, then the coefficient is likely <0.

Get the partial likelihood of a Cox PH Model with new data

offset was used. See https://stackoverflow.com/questions/26721551/is-there-a-way-to-get-the-partial-likelihood-of-a-cox-ph-model-with-new-data-and

How to compute partial log-likelihood function in Cox proportional hazards model?

set.seed(1)
n <- 1000
t <- rexp(100)
c <- rbinom(100, 1, .2) ## censoring indicator (independent process)
x <- rbinom(100, 1, exp(-t)) ## some arbitrary relationship btn x and t
betamax <- coxph(Surv(t, c) ~ x)
beta1 <- coxph(Surv(t, c) ~ x, init = c(1), control=coxph.control(iter.max=0))

betamax$loglik[2]  # [1]=initial, [2]=final
# [1] -52.81476
beta1$loglik[2]
# [1] -52.85067

Implementing the Cox model

Implementing the Cox model in R

Optimization

Optimisation of a Cox proportional hazard model using Optimx()

Compare the partial likelihood to the full likelihood

http://math.ucsd.edu/~rxu/math284/slect5.pdf#page=10

z-column (Wald statistic) from R's coxph()

https://socialsciences.mcmaster.ca/jfox/Books/Companion/appendix/Appendix-Cox-Regression.pdf#page=6 The ratio of each regression coefficient to its standard error, a Wald statistic which is asymptotically standard normal under the hypothesis that the corresponding β is 0.
http://dni-institute.in/blogs/cox-regression-interpret-result-and-predict/

How exactly can the Cox-model ignore exact times?

The Cox model does not depend on the times itself, instead it only needs an ordering of the events.

library(survival)
survfit(Surv(time, status) ~ x, data = aml) 
fit <- coxph(Surv(time, status) ~ x, data = aml)
coef(fit) # 0.9155326
min(diff(sort(unique(aml$time)))) # 1

# Shift survival time for some obs but keeps the same order
# make sure we choose obs (n=20 not works but n=21 works) with twins
rbind(order(aml$time), sort(aml$time), aml$time[order(aml$time)])
# [,1] [,2] [,3] [,4] [,5] [,6] [,7] [,8] [,9] [,10] [,11] [,12] [,13] [,14] [,15] [,16]
# [1,]   12   13   14   15    1   16    2    3   17     4     5    18    19     6    20     7
# [2,]    5    5    8    8    9   12   13   13   16    18    23    23    27    28    30    31
# [3,]    5    5    8    8    9   12   13   13   16    18    23    23    27    28    30    31
# [,17] [,18] [,19] [,20] [,21] [,22] [,23]
# [1,]    21     8    22     9    23    10    11
# [2,]    33    34    43    45    45    48   161
# [3,]    33    34    43    45    45    48   161

aml$time2 <- aml$time
aml$time2[order(aml$time)[1:21]] <- aml$time[order(aml$time)[1:21]] - .9
fit2 <- coxph(Surv(time2, status) ~ x, data = aml); fit2
coef(fit2) #      0.9155326
coef(fit) == coef(fit2) # TRUE

aml$time3 <- aml$time 
aml$time3[order(aml$time)[1:20]] <- aml$time[order(aml$time)[1:20]] - .9
fit3 <- coxph(Surv(time3, status) ~ x, data = aml); fit3
coef(fit3) #      0.8891567
coef(fit) == coef(fit3) # FALSE

Partial likelihood when there are ties; hypothesis testing: Likelihood Ratio Test, Wald Test & Score Test

http://math.ucsd.edu/~rxu/math284/slect5.pdf#page=29

In R's coxph(): Nearly all Cox regression programs use the Breslow method by default, but not this one. The Efron approximation is used as the default here, it is more accurate when dealing with tied death times, and is as efficient computationally.

http://sfb649.wiwi.hu-berlin.de/fedc_homepage/xplore/tutorials/xaghtmlnode28.html (include the case when there is a partition of parameters). The formulas for 3 tests are also available on Appendix B of Klein book.

The following code does not test for models. But since there is only one coefficient, the results are the same. If there is more than one variable, we can use anova(model1, model2) to run LRT.

library(KMsurv)
# No ties. Section 8.2
data(btrial)
str(btrial)
# 'data.frame':	45 obs. of  3 variables:
# $ time : int  19 25 30 34 37 46 47 51 56 57 ...
# $ death: int  1 1 1 1 1 1 1 1 1 1 ...
# $ im   : int  1 1 1 1 1 1 1 1 1 1 ...
table(subset(btrial, death == 1)$time)
# death time is unique
coxph(Surv(time, death) ~ im, data = btrial)
#     coef exp(coef) se(coef)    z     p
# im 0.980     2.665    0.435 2.25 0.024
# Likelihood ratio test=4.45  on 1 df, p=0.03
# n= 45, number of events= 24 

# Ties, Section 8.3
data(kidney)
str(kidney)
# 'data.frame':	119 obs. of  3 variables:
# $ time : num  1.5 3.5 4.5 4.5 5.5 8.5 8.5 9.5 10.5 11.5 ...
# $ delta: int  1 1 1 1 1 1 1 1 1 1 ...
# $ type : int  1 1 1 1 1 1 1 1 1 1 ...
table(subset(kidney, delta == 1)$time)
# 0.5  1.5  2.5  3.5  4.5  5.5  6.5  8.5  9.5 10.5 11.5 15.5 16.5 18.5 23.5 26.5 
# 6    1    2    2    2    1    1    2    1    1    1    2    1    1    1    1 

# Default: Efron method
coxph(Surv(time, delta) ~ type, data = kidney)
# coef exp(coef) se(coef)     z    p
# type -0.613     0.542    0.398 -1.54 0.12
# Likelihood ratio test=2.41  on 1 df, p=0.1
# n= 119, number of events= 26 
summary(coxph(Surv(time, delta) ~ type, data = kidney))
# n= 119, number of events= 26 
# coef exp(coef) se(coef)      z Pr(>|z|)
# type -0.6126    0.5420   0.3979 -1.539    0.124
#
# exp(coef) exp(-coef) lower .95 upper .95
# type     0.542      1.845    0.2485     1.182
#
# Concordance= 0.497  (se = 0.056 )
# Rsquare= 0.02   (max possible= 0.827 )
# Likelihood ratio test= 2.41  on 1 df,   p=0.1
# Wald test            = 2.37  on 1 df,   p=0.1
# Score (logrank) test = 2.44  on 1 df,   p=0.1

# Breslow method
summary(coxph(Surv(time, delta) ~ type, data = kidney, ties = "breslow"))
# n= 119, number of events= 26 
#         coef exp(coef) se(coef)      z Pr(>|z|)
# type -0.6182    0.5389   0.3981 -1.553     0.12
#
#       exp(coef) exp(-coef) lower .95 upper .95
# type    0.5389      1.856     0.247     1.176
#
# Concordance= 0.497  (se = 0.056 )
# Rsquare= 0.02   (max possible= 0.827 )
# Likelihood ratio test= 2.45  on 1 df,   p=0.1
# Wald test            = 2.41  on 1 df,   p=0.1
# Score (logrank) test = 2.49  on 1 df,   p=0.1

# Discrete/exact method
summary(coxph(Surv(time, delta) ~ type, data = kidney, ties = "exact"))
#         coef exp(coef) se(coef)      z Pr(>|z|)
# type -0.6294    0.5329   0.4019 -1.566    0.117
#
#      exp(coef) exp(-coef) lower .95 upper .95
# type    0.5329      1.877    0.2424     1.171
#
# Rsquare= 0.021   (max possible= 0.795 )
# Likelihood ratio test= 2.49  on 1 df,   p=0.1
# Wald test            = 2.45  on 1 df,   p=0.1
# Score (logrank) test = 2.53  on 1 df,   p=0.1

Hazard (function) and survival function

A hazard is the rate at which events happen, so that the probability of an event happening in a short time interval is the length of time multiplied by the hazard.

[math]\displaystyle{ h(t) = \lim_{\Delta t \to 0} \frac{P(t \leq T \lt t+\Delta t|T \geq t)}{\Delta t} = \frac{f(t)}{S(t)} = -\partial{ln[S(t)]} }[/math]

Therefore

[math]\displaystyle{ H(x) = \int_0^x h(u) d(u) = -ln[S(x)]. }[/math]

or

[math]\displaystyle{ S(x) = e^{-H(x)} }[/math]

Hazards (or probability of hazards) may vary with time, while the assumption in proportional hazard models for survival is that the hazard is a constant proportion.

Examples:

If h(t)=c, S(t) is exponential. f(t) = c exp(-ct). The mean is 1/c.
If [math]\displaystyle{ \log h(t) = c + \rho t }[/math], S(t) is Gompertz distribution.
If [math]\displaystyle{ \log h(t)=c + \rho \log (t) }[/math], S(t) is Weibull distribution.
For Cox regression, the survival function can be shown to be [math]\displaystyle{ S(t|X) = S_0(t) ^ {\exp(X\beta)} }[/math].

[math]\displaystyle{ \begin{align} S(t|X) &= e^{-H(t)} = e^{-\int_0^t h(u|X)du} \\ &= e^{-\int_0^t h_0(u) exp(X\beta) du} \\ &= e^{-\int_0^t h_0(u) du \cdot exp(X \beta)} \\ &= S_0(t)^{exp(X \beta)} \end{align} }[/math]

Alternatively,

[math]\displaystyle{ \begin{align} S(t|X) &= e^{-H(t)} = e^{-\int_0^t h(u|X)du} \\ &= e^{-\int_0^t h_0(u) exp(X\beta) du} \\ &= e^{-H_0(t) \cdot exp(X \beta)} \end{align} }[/math]

where the cumulative baseline hazard at time t, [math]\displaystyle{ H_0(t) }[/math], is commonly estimated through the non-parametric Breslow estimator.

How to assess Cox model fit

Survival Analysis in R for Public Health from Coursera
Evaluating goodness-of-fit in comparison to a null model
A Graphical Method for Assessing Goodness of Fit in Cox's Proportional Hazards Model Arjas JASA 1988
Evaluation of Goodness-of-fit Tests for the Cox Proportional Hazards Model with Time-Varying Covariates
Assessment of the fitness of Cox and parametric regression models of survival distribution for Iranian breast cancer patients' data

Check the proportional hazard (constant HR over time) assumption by cox.zph() - Schoenfeld Residuals

It seems to be predictor specific.
Survival Analysis Tutorial by Jacob Lindell and Joe Berry.
Log-log Kaplan-Meier curves and other methods.
https://stats.idre.ucla.edu/other/examples/asa2/testing-the-proportional-hazard-assumption-in-cox-models/. If the predictor satisfy the proportional hazard assumption then the graph of the survival function versus the survival time should results in a graph with parallel curves, similarly the graph of the log(-log(survival)) versus log of survival time graph should result in parallel lines if the predictor is proportional. This method does not work well for continuous predictor or categorical predictors that have many levels because the graph becomes to “cluttered”.

Methods to evaluate the validity of the Cox model assumptions, Assessing proportional hazards

library(survival)
res.cox <- coxph(Surv(time, status) ~ age + sex + wt.loss, data =  lung)

# A hypothesis test of whether the effect of each covariate differs according to time,
# and a global test of all covariates at once.
cz <- cox.zph(res.cox); cz
plot(cz) # it will draw 3 plots; one for each variable
         # y-axis is beta(t), x = time
plot(cz[3]]) # 3rd variable

Complementary log-log survival curve . ?plot(survfit(formula), fun). For example fun="cloglog" will create a complimentary log-log survival plot (log(-log(S(t))) along with log(t) in the x-axis).
- If we don't like the log scale for the x-axis, we can write our own function; see R survival package; plotting log(-log(survival)) against log(time)
- 3.6 How to evaluate the PH assumption? from "A short course on Survival Analysis applied to the Financial Industry"
- Use strata() in coxph() to stratify on one covariate and plot the two baseline hazards.
Schoenfeld residuals - Plain English explanation, please! If the plot is reasonably flat over time, the PH assumption holds.
- The Schoenfeld Residuals Test is analogous to testing whether the slope of scaled residuals on time is zero or not. If the plot of Schoenfeld residuals against time shows a non-random pattern, the PH assumption has been violated. See Schoenfeld Residuals Test - Meaning & Definition

survival package
- cox.zph()
- residuals()
timereg package. Flexible Regression Models for Survival Data.
- timereg::cum.residuals()
Draw a hazard rate plot. [math]\displaystyle{ \begin{align} \log(−\log(𝑆(𝑡))) = \log(−\log(S_0(𝑡))) + \beta X \end{align} }[/math]
- How to calculate predicted hazard rates from a Cox PH model?. The hazard ratio should be constant; h(t|Z) / h(t|Z*) is independent of t.
- See an example of non-proportional hazards where the KM curves cross.
- More graphical examples where log-log survival curves are not parallel. A short course on Survival Analysis applied to the Financial Industry.
- Two plots where one shows the assumption is violated. Proportionality assumption in Cox Regression Model
- log cumulative hazard plot. An example where PH is not satisfied.
Looking at the Kaplan-Meier curves (Survival probability vs time). If the (discrete) predictor satisfy the proportional hazard assumption then the graph of the survival function versus the survival time should results in a graph with parallel curves, similarly the graph of the log(-log(survival)) versus log of survival time graph should result in parallel lines if the predictor is proportional. UCLA.
An online updating approach for testing the proportional hazards assumption with streams of survival data Xue 2019
https://www.rdocumentation.org/packages/gof/versions/0.9.1/topics/cumres.coxph
http://rstudio-pubs-static.s3.amazonaws.com/5043_145684af0d364175bf5e5e6bb792ca28.html
Residuals and model diagnostics from the lecture notes of Patrick Breheny
Assessing the Fit of the Cox Model from the lecture notes of Ronghui Xu
Cumulative martingale residuals (Lin et al Biometrika 1993)
Violations of proportional hazard assumption in Cox regression model of transcriptomic data in TCGA pan-cancer cohorts 2022
Assumption-Lean Cox Regression JASA 2022

Strata, Stratification

Stratification in the Cox model Patrick Breheny
stratification in cox model. In a Cox model, stratification allows for as many different hazard functions as there are strata. Beta coefficients (hazard ratios) optimized for all strata are then fitted.
Stratification example

bladder1 <- bladder[bladder$enum < 5, ] 
o <- coxph(Surv(stop, event) ~ rx + size + number + strata(enum) , bladder1)
# the strata will not be a term in covariate in the model fitting
anova(o)

Sample size calculators

Calculate Sample Size Needed to Test Time-To-Event Data: Cox PH, Equivalence including a reference
http://www.sample-size.net/sample-size-survival-analysis/ including a reference
Evolution of survival sample size methods demonstrated by nQuery software. Sample size refers the number of events; status=1 (not the number of observations)
http://www.icssc.org/Documents/AdvBiosGoa/Tab%2026.00_SurvSS.pdf no reference
powerSurvEpi R package
NPHMC R package (based on the Proportional Hazards Mixture Cure Model) and the paper
Hmisc::cpower() function.

How many events are required to fit the Cox regression reliably?

The recommended number of events to fit a Cox regression model for survival data is typically guided by a rule of thumb. This rule suggests having at least 10-20 events per predictor in the model; see Survival analysis with rare events.

If we have only 1 covariate and the covariate is continuous, we need at least 2 events (one for the baseline hazard and one for beta).

If the covariate is discrete, we need at least one event from (each of) two groups in order to fit the Cox regression reliably. For example, if status=(0,0,0,1,0,1) and x=(0,0,1,1,2,2) works fine.

library(survival)
head(ovarian)
#   futime fustat     age resid.ds rx ecog.ps
# 1     59      1 72.3315        2  1       1
# 2    115      1 74.4932        2  1       1
# 3    156      1 66.4658        2  1       2
# 4    421      0 53.3644        2  2       1
# 5    431      1 50.3397        2  1       1
# 6    448      0 56.4301        1  1       2

ova <- ovarian # n=26
ova$time <- ova$futime
ova$status <- 0
ova$status[1:4] <- 1
coxph(Surv(time, status) ~ rx, data = ova) # OK
summary(survfit(Surv(time, status) ~ rx, data =ova))
#                 rx=1 
#  time n.risk n.event survival std.err lower 95% CI upper 95% CI
#    59     13       1    0.923  0.0739        0.789            1
#   115     12       1    0.846  0.1001        0.671            1
#   156     11       1    0.769  0.1169        0.571            1
#                 rx=2 
#     time  n.risk  n.event  survival  std.err lower 95% CI upper 95% CI 
# 421.0000 10.0000   1.0000    0.9000   0.0949       0.7320       1.0000 

# Suspicious Cox regression result due to 0 sample size in one group
ova$status <- 0
ova$status[1:3] <- 1
coxph(Surv(time, status) ~ rx, data = ova)
#         coef exp(coef)  se(coef) z p
# rx -2.13e+01  5.67e-10  2.32e+04 0 1
#
# Likelihood ratio test=4.41  on 1 df, p=0.04
# n= 26, number of events= 3 
# Warning message:
# In fitter(X, Y, strats, offset, init, control, weights = weights,  :
#   Loglik converged before variable  1 ; beta may be infinite. 

summary(survfit(Surv(time, status) ~ rx, data = ova))
#                rx=1 
# time n.risk n.event survival std.err lower 95% CI upper 95% CI
#   59     13       1    0.923  0.0739        0.789            1
#  115     12       1    0.846  0.1001        0.671            1
#  156     11       1    0.769  0.1169        0.571            1
#                rx=2 
# time n.risk n.event survival std.err lower 95% CI upper 95% CI

Extract p-values

fit <- coxph(Surv(futime, fustat) ~ age, data = ovarian)

# method 1:
beta <- coef(fit)
se <- sqrt(diag(vcov(fit)))
1 - pchisq((beta/se)^2, 1)

# method 2: https://www.biostars.org/p/65315/
coef(summary(fit))[, "Pr(>|z|)"]

More statistics including the HR confidence intervals.

Expectation of life & expected future lifetime

The average lifetime is the same as the area under the survival curve.

[math]\displaystyle{ \begin{align} \mu &= \int_0^\infty t f(t) dt \\ &= \int_0^\infty S(t) dt \end{align} }[/math]

by integrating by parts making use of the fact that -f(t) is the derivative of S(t), which has limits S(0)=1 and [math]\displaystyle{ S(\infty)=0 }[/math]. The average lifetime may not be bounded if you have censored data, there's censored observations that last beyond your last recorded death.

The expected future lifetime at a given time [math]\displaystyle{ t_0 }[/math]

[math]\displaystyle{ \frac{1}{S(t_0)} \int_0^{\infty} t\,f(t_0+t)\,dt = \frac{1}{S(t_0)} \int_{t_0}^{\infty} S(t)\,dt, }[/math]

Hazard Ratio (exp^beta) vs Relative Risk

https://en.wikipedia.org/wiki/Hazard_ratio
Hazard represents the instantaneous event rate, which means the probability that an individual would experience an event (e.g. death/relapse) at a particular given point in time after the intervention, assuming that this individual has survived to that particular point of time without experiencing any event. See an example here.
Hazard ratio is a measure of an effect of an intervention of an outcome of interest over time. The hazard ratio is not computed at any one time point. See an example here.
Since there is only one hazard ratio reported, it can can only be interpreted if you assume that the population hazard ratio is consistent over time, and that any differences are due to random sampling. If two survival curves cross, the hazard ratios are certainly not consistent. See Hazard ratio from survival analysis including how the hazard ratio is computed.
Hazard ratio = hazard in the intervention group / Hazard in the control group
A hazard ratio is often reported as a “reduction in risk of death or progression” – This risk reduction is calculated as 1 minus the Hazard Ratio (exp^beta), e.g., HR of 0.84 is equal to a 16% reduction in risk. See this video Interpreting Hazard Ratios and stackexchange.com.
If the hazard ratio for overall survival (OS) from initiation of therapy for patients with BRCAm vs BRCAwt is 0.812, this means that, at any given time point, the hazard of death (or event of interest) for patients with BRCAm is 0.81 times the hazard of death for patients with BRCAwt. In other words, patients with BRCAm have a 19% lower risk of death at any time point compared to patients with BRCAwt. Prevalence and prognosis of BRCAm, homologous recombination repair mutation (HRRm) or HR deficiency positive (HRD+) across tumor types.
- BRCA-tested patients had a lower risk of death versus untested (HR 0.35, 95 % CI 0.17, 0.68, p = 0.001). “BRCA-tested patients” does not necessarily mean these patients have a BRCA mutation. It simply means these patients have undergone testing BRCA mutations.
Hazard ratio and its confidence can be obtained in R by using the summary() method; e.g. fit <- coxph(Surv(time, status) ~ x); summary(fit)$conf.int; confint(fit)
The coefficient beta represents the expected change in log hazard if X changes by one unit and all other variables are held constant in Cox models. See Variable selection – A review and recommendations for the practicing statistician by Heinze et al 2018.
Understanding the endpoints in oncology: overall survival, progression free survival, hazard ratio, censored value

Another example (John Fox, Cox Proportional-Hazards Regression for Survival Data) is assuming Y ~ age + prio + others.

If exp(beta_age) = 0.944. It means an additional year of age reduces the hazard by a factor of .944 on average, or (1-.944)*100 = 5.6 percent.
If exp(beta_prio) = 1.096, it means each prior conviction increases the hazard by a factor of 1.096, or 9.6 percent.

How do you explain the difference between hazard ratio and relative risk to a layman? from Quora.

See Using R for Biomedical Statistics for relative risk, odds ratio, et al.

Odds Ratio, Hazard Ratio and Relative Risk by Janez Stare

For two groups that differ only in treatment condition, the ratio of the hazard functions is given by [math]\displaystyle{ e^\beta }[/math], where [math]\displaystyle{ \beta }[/math] is the estimate of treatment effect derived from the regression model. See here.

Compute ratio ratios from coxph() in R (Hint: exp(beta)).

Prognostic index is defined on http://www.math.ucsd.edu/~rxu/math284/slect6.pdf#page=2.

Basics of the Cox proportional hazards model. Good prognostic factor (b<0 or HR<1) and bad prognostic factor (b>0 or HR>1).

Variable selection: variables were retained in the prediction models if they had a hazard ratio of <0.85 or >1.15 (for binary variables) and were statistically significant at the 0.01 level. see Development and validation of risk prediction equations to estimate survival in patients with colorectal cancer: cohort study.

library(KMsurv)
# No ties. Section 8.2
data(btrial)
coxph(Surv(time, death) ~ im, data = btrial)
summary(coxph(Surv(time, death) ~ im, data = btrial))$conf.int
#     exp(coef) exp(-coef) lower .95 upper .95
# im  2.664988  0.3752362  1.136362  6.249912

So the hazard ratio and its 95% ci can be obtained from the 1st, 3rd and 4th element in conf.int.

Hazard Ratio, confidence interval, Table 1

Google image: survival data cox model hazard ratio table 1

To get the 95% CI, use the summary() function

> mod = coxph(Surv(time,status) ~ x, data = aml)
> summary(mod)
  n= 23, number of events= 18 

                 coef exp(coef) se(coef)     z Pr(>|z|)  
xNonmaintained 0.9155    2.4981   0.5119 1.788   0.0737 .
---
Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1

               exp(coef) exp(-coef) lower .95 upper .95
xNonmaintained     2.498     0.4003    0.9159     6.813

Concordance= 0.619  (se = 0.063 )
Likelihood ratio test= 3.38  on 1 df,   p=0.07
Wald test            = 3.2  on 1 df,   p=0.07
Score (logrank) test = 3.42  on 1 df,   p=0.06

Naive method (wrong) to calculate the hazard ratio

> with(aml, table(x, status))
               status
x                0  1
  Maintained     4  7
  Nonmaintained  1 11
> (11/12) / (7/11)  # hazard from the 2nd group / hazard from the 1st group
[1] 1.440476

To report the HR in table 1 for multiple variables, one must use Univariate Cox regression; for example this one uses lapply().

Hazard Ratio and death probability

https://en.wikipedia.org/wiki/Hazard_ratio#The_hazard_ratio_and_survival

Suppose S₀(t)=.2 (20% survived at time t) and the hazard ratio (hr) is 2 (a group has twice the chance of dying than a comparison group), then (Cox model is assumed)

S₁(t)=S₀(t)^hr = .2² = .04 (4% survived at t)
The corresponding death probabilities are 0.8 and 0.96.
If a subject is exposed to twice the risk of a reference subject at every age, then the probability that the subject will be alive at any given age is the square of the probability that the reference subject (covariates = 0) would be alive at the same age. See p10 of this lecture notes.
exp(x*beta) is the relative risk associated with covariate value x.

Hazard Ratio Forest Plot

The forest plot quickly summarizes the hazard ratio data across multiple variables –If the line crosses the 1.0 value, the hazard ratio is not significant and there is no clear advantage for either arm.

See also ggplot2 forest plot. survminer::ggforest(), survivalAnalysis::forest_plot() and forestmodel::forest_model().

library(survival)
library(survivalAnalysis)
library(survminer)
data(cancer, package = 'survival') # load colon among others
colon$sex <- factor(colon$sex)

tmp1 <- survival::colon %>%
   analyse_multivariate(vars(time, status),
      vars(rx, sex, age, obstruct, perfor, nodes, differ, extent)) 
tmp1 %>% forest_plot()

tmp2 <- coxph(Surv(time, status) ~ rx + sex + age + obstruct + 
     perfor + nodes + differ + extent, data=colon)
survminer::ggforest(tmp2, data = colon)

# Note that the above is not quite right since it is not based on 
# the univariate model
coxph(Surv(time, status) ~ sex, data  = colon)

# Even if all are continuous, fitting univariate and multivariate models
# returns different results
coxph(Surv(time, status) ~ obstruct, data  = colon)
coxph(Surv(time, status) ~ obstruct + perfor + age, data  = colon)

So the problem with survminer::ggforest() is it cannot run univariate Cox model for multiple variables. survivalAnalysis package can do that but I need to make sure the data looks correct (e.g. change 'unknown' to data that should be a continuous value). See the section "Multiple Univariate Analyses" in the Multivariate Survival Analysis vignette.

df <- survival::lung %>% 
  mutate(sex=rename_factor(sex, `1` = "male", `2` = "female"))

map(vars(age, sex, ph.ecog, wt.loss), function(by)
{
  analyse_multivariate(df,
                       vars(time, status),
                       covariates = list(by), # covariates expects a list
                       covariate_name_dict = covariate_names)
}) %>%
  forest_plot(factor_labeller = covariate_names,
              endpoint_labeller = c(time="OS"),
              orderer = ~order(HR),
              labels_displayed = c("endpoint", "factor", "n"),
              ggtheme = ggplot2::theme_bw(base_size = 10))

Other examples:

Forest Plot for a Meta-analysis of Several Different Randomised Control Trials. See Using R for Biomedical Statistics
Predictors for efficacy in BRCA1/2 wild-type participants

Multivariate model

Variables order does not change the hazard ratios or the p-value

R> data(cancer, package = 'survival') # load colon among others
R> colon$sex <- factor(colon$sex)
R> tmp2 <- coxph(Surv(time, status) ~ rx + sex + age + obstruct + 
                 perfor + nodes + differ + extent, data=colon)
R> tmp2
Call:
coxph(formula = Surv(time, status) ~ rx + sex + age + obstruct +
    perfor + nodes + differ + extent, data = colon)

               coef exp(coef)  se(coef)      z        p
rxLev     -0.072841  0.929749  0.079231 -0.919   0.3579
rxLev+5FU -0.450133  0.637543  0.085975 -5.236 1.64e-07
sex1      -0.090141  0.913803  0.068075 -1.324   0.1855
age        0.002164  1.002166  0.002874  0.753   0.4516
obstruct   0.202638  1.224629  0.084372  2.402   0.0163
perfor     0.149875  1.161689  0.182766  0.820   0.4122
nodes      0.081185  1.084571  0.006698 12.120  < 2e-16
differ     0.146674  1.157977  0.070095  2.093   0.0364
extent     0.467536  1.596057  0.081726  5.721 1.06e-08

Likelihood ratio test=212.6  on 9 df, p=< 2.2e-16
n= 1776, number of events= 876
   (82 observations deleted due to missingness)

# Move 'nodes' to the last term
R> tmp3 <- coxph(Surv(time, status) ~ rx + sex + age + obstruct +
                 perfor + differ + extent + nodes, data=colon)
R> tmp3
Call:
coxph(formula = Surv(time, status) ~ rx + sex + age + obstruct +
    perfor + differ + extent + nodes, data = colon)

               coef exp(coef)  se(coef)      z        p
rxLev     -0.072841  0.929749  0.079231 -0.919   0.3579
rxLev+5FU -0.450133  0.637543  0.085975 -5.236 1.64e-07
sex1      -0.090141  0.913803  0.068075 -1.324   0.1855
age        0.002164  1.002166  0.002874  0.753   0.4516
obstruct   0.202638  1.224629  0.084372  2.402   0.0163
perfor     0.149875  1.161689  0.182766  0.820   0.4122
differ     0.146674  1.157977  0.070095  2.093   0.0364
extent     0.467536  1.596057  0.081726  5.721 1.06e-08
nodes      0.081185  1.084571  0.006698 12.120  < 2e-16

Likelihood ratio test=212.6  on 9 df, p=< 2.2e-16
n= 1776, number of events= 876
   (82 observations deleted due to missingness)

Univariate model and multivariate model result diff

R> coxph(Surv(time, status) ~ perfor, data = colon)
Call:
coxph(formula = Surv(time, status) ~ perfor, data = colon)

         coef exp(coef) se(coef)     z     p
perfor 0.2644    1.3026   0.1800 1.469 0.142

Likelihood ratio test=1.99  on 1 df, p=0.1583
n= 1858, number of events= 920
R> coxph(Surv(time, status) ~ age + perfor, data = colon)
Call:
coxph(formula = Surv(time, status) ~ age + perfor, data = colon)

            coef exp(coef)  se(coef)      z     p
age    -0.002325  0.997678  0.002797 -0.831 0.406
perfor  0.259370  1.296113  0.180067  1.440 0.150

Likelihood ratio test=2.68  on 2 df, p=0.2621
n= 1858, number of events= 920

Infinity HR

Monotone likelihood and coxphf package.

Piece-wise constant baseline hazard model, Poisson model and Breslow estimate

https://en.wikipedia.org/wiki/Proportional_hazards_model#Relationship_to_Poisson_models
Poisson regression
http://data.princeton.edu/wws509/notes/c7s4.html
It has been implemented in the biospear package (poissonize.R) with the 'grplasso' package for group-lasso method. We implemented a Poisson model over two-month intervals, corresponding to a piecewise constant hazard model which approximates rather well the Breslow estimator in the Cox model.
http://r.789695.n4.nabble.com/exponential-proportional-hazard-model-td805536.html
https://www.demogr.mpg.de/papers/technicalreports/tr-2010-003.pdf
Does Cox Regression have an underlying Poisson distribution?
- Calculate incidence rates using poisson model: relation to hazard ratio from Cox PH model R code verification is included.
Glm family functions in glmnet 4.0 also mentions Cox model (and multinomial regression, and multi-response Gaussian) is a special case of the Poisson GLM.
https://rdrr.io/cran/JM/man/piecewiseExp.ph.html
https://rdrr.io/cran/pch/man/pchreg.html
Survival Analysis via Hazard Based Modeling and Generalized Linear Models
https://www.rdocumentation.org/packages/mgcv/versions/1.8-23/topics/cox.pht
Optimisation of a Poisson survival model using Optimx in R

Estimate baseline hazard [math]\displaystyle{ h_0(t) }[/math], Breslow cumulative baseline hazard [math]\displaystyle{ H_0(t) }[/math], baseline survival function [math]\displaystyle{ S_0(t) }[/math] and the survival function [math]\displaystyle{ S(t) }[/math]

Google: how to estimate baseline hazard rate

survfit.object has print(), plot(), lines(), and points() methods. It returns a list with components
- n
- time
- n.risk
- n.event
- n.censor
- surv [S_0(t)]
- cumhaz [ same as -log(surv)]
- upper
- lower
- n.all
Terry Therneau: The baseline survival, which is the survival for a hypothetical subject with all covariates=0, may be useful mathematical shorthand when writing a book but I cannot think of a single case where the resulting curve would be of any practical interest in medical data.
http://www.math.ucsd.edu/~rxu/math284/slect6.pdf#page=4 Breslow Estimator for cumulative baseline hazard at a time t and Kalbfleisch/Prentice Estimator
When there are no covariates, the Breslow’s estimate reduces to the Fleming-Harrington (Nelson-Aalen) estimate, and K/P reduces to KM.
stackexchange.com and cumulative and non-cumulative baseline hazard
(newbie) Cox Baseline Hazard There are two methods of calculating the baseline survival, the default one gives the baseline hazard estimator you want. It is attributed to Aalen, Breslow, or Peto (see the next item). An example: https://stats.idre.ucla.edu/r/examples/asa/r-applied-survival-analysis-ch-2/.
survfit.coxph(formula, newdata, type, ...)
- newdata: Default is the mean of the covariates used in the coxph fit
- type = "aalen", "efron", or "kalbfleisch-prentice". The default is to match the computation used in the Cox model. The Nelson-Aalen-Breslow estimate for ties='breslow', the Efron estimate for ties='efron' and the Kalbfleisch-Prentice estimate for a discrete time model ties='exact'. Variance estimates are the Aalen-Link-Tsiatis, Efron, and Greenwood. The default will be the Efron estimate for ties='efron' and the Aalen estimate otherwise.

Nelson-Aalen estimator in R. The easiest way to get the Nelson-Aalen estimator is
```
basehaz(coxph(Surv(time,status)~1,data=aml)) 
```
because the (Breslow) hazard estimator for a Cox model reduces to the Nelson-Aalen estimator when there are no covariates. You can also compute it from information returned by survfit().
```
fit <- survfit(Surv(time, status) ~ 1, data = aml)
cumsum(fit$n.event/fit$n.risk) # the Nelson-Aalen estimator for the times given by fit$times
-log(fit$surv)   # cumulative hazard
```

Manually compute

Breslow estimator of the baseline cumulative hazard rate reduces to the Nelson-Aalen estimator [math]\displaystyle{ \sum_{t_i \le t} \frac{d_i}{Y_i} }[/math] ([math]\displaystyle{ Y_i }[/math] is the number at risk at time [math]\displaystyle{ t_i }[/math]) when there are no covariates present; see p283 of Klein 2003.

[math]\displaystyle{ \begin{align} \hat{H}_0(t) &= \sum_{t_i \le t} \frac{d_i}{W(t_i;b)}, \\ W(t_i;b) &= \sum_{j \in R(t_i)} \exp(b' z_j) \end{align} }[/math]

where [math]\displaystyle{ t_1 \lt t_2 \lt \cdots \lt t_D }[/math] denotes the distinct death times and [math]\displaystyle{ d_i }[/math] be the number of deaths at time [math]\displaystyle{ t_i }[/math]. The estimator of the baseline survival function [math]\displaystyle{ S_0(t) = \exp [-H_0(t)] }[/math] is given by [math]\displaystyle{ \hat{S}_0(t) = \exp [-\hat{H}_0(t)] }[/math].

Below we use the formula to compute the cumulative hazard (and survival function) and compare them with the result obtained using R's built-in functions. The following code is a modification of the snippet from the post Breslow cumulative hazard and basehaz().

bhaz <- function(beta, time, status, x) {
  # time can be duplicated
  # x (covariate) must be continuous
  data <- data.frame(time,status,x)
  data <- data[order(data$time), ]
  dt   <- unique(data$time)
  k    <- length(dt)
  risk <- exp(data.matrix(data[,-c(1:2)]) %*% beta)
  h    <- rep(0,k)
  
  for(i in 1:k) {
    h[i] <- sum(data$status[data$time==dt[i]]) / sum(risk[data$time>=dt[i]])          
  }
  
  return(data.frame(h, dt))
}

# Example 1 'ovarian' which has unique survival time
all(table(ovarian$futime) == 1) # TRUE

fit <- coxph(Surv(futime, fustat) ~ age, data = ovarian)
# 1. compute the cumulative baseline hazard 
# 1.1 manually using Breslow estimator at the observed time
h0 <- bhaz(fit$coef, ovarian$futime, ovarian$fustat, ovarian$age)
H0 <- cumsum(h0$h)
# 1.2 use basehaz (always compute at the observed time)
# since we consider the baseline, we need to use centered=FALSE
H0.bh <- basehaz(fit, centered = FALSE)
cbind(H0, h0$dt, H0.bh)
range(abs(H0 - H0.bh$hazard)) # [1] 6.352747e-22 5.421011e-20

# 2. compute the estimation of the survival function
# 2.1 manually using Breslow estimator at t = observed time (one dim, sorted) 
#     and observed age (another dim):
# S(t) = S0(t) ^ exp(bx) = exp(-H0(t)) ^ exp(bx)
S1 <- outer(exp(-H0),  exp(coef(fit) * ovarian$age), "^")
dim(S1) # row = times, col = age
# 2.2 How about considering times not at observed (e.g. h0$dt - 10)?
# Let's look at the hazard rate
newtime <- h0$dt - 10
H0 <- sapply(newtime, function(tt) sum(h0$h[h0$dt <= tt]))
S2 <- outer(exp(-H0),  exp(coef(fit) * ovarian$age), "^")
dim(S2) # row = newtime, col = age

# 2.3 use summary() and survfit() to obtain the estimation of the survival
S3 <- summary(survfit(fit, data.frame(age = ovarian$age)), times = h0$dt)$surv
dim(S3)  # row = times, col = age
range(abs(S1 - S3)) # [1] 2.117244e-17 6.544321e-12
# 2.4 How about considering times not at observed (e.g. h0$dt - 10)?
# Note that we cannot put times larger than the observed
S4 <- summary(survfit(fit, data.frame(age = ovarian$age)), times = newtime)$surv
range(abs(S2 - S4)) # [1] 0.000000e+00 6.544321e-12

# Example 2 'kidney' which has duplicated time
fit <- coxph(Surv(time, status) ~ age, data = kidney)
# manually compute the breslow cumulative baseline hazard
#   at the observed time
h0 <- with(kidney, bhaz(fit$coef, time, status, age))
H0 <- cumsum(h0$h)
# use basehaz (always compute at the observed time)
# since we consider the baseline, we need to use centered=FALSE
H0.bh <- basehaz(fit, centered = FALSE)
head(cbind(H0, h0$dt, H0.bh))
range(abs(H0 - H0.bh$hazard)) # [1] 0.000000000 0.005775414

# manually compute the estimation of the survival function
# at t = observed time (one dim, sorted) and observed age (another dim):
# S(t) = S0(t) ^ exp(bx) = exp(-H0(t)) ^ exp(bx)
S1 <- outer(exp(-H0),  exp(coef(fit) * kidney$age), "^")
dim(S1) # row = times, col = age
# How about considering times not at observed (h0$dt - 1)?
# Let's look at the hazard rate
newtime <- h0$dt - 1
H0 <- sapply(newtime, function(tt) sum(h0$h[h0$dt <= tt]))
S2 <- outer(exp(-H0),  exp(coef(fit) * kidney$age), "^")
dim(S2) # row = newtime, col = age

# use summary() and survfit() to obtain the estimation of the survival
S3 <- summary(survfit(fit, data.frame(age = kidney$age)), times = h0$dt)$surv
dim(S3)  # row = times, col = age
range(abs(S1 - S3)) # [1] 0.000000000 0.002783715
# How about considering times not at observed (h0$dt - 1)?
# We cannot put times larger than the observed
S4 <- summary(survfit(fit, data.frame(age = kidney$age)), times = newtime)$surv
range(abs(S2 - S4)) # [1] 0.000000000 0.002783715

basehaz() (an alias for survfit) from stackexchange.com and here. basehaz() has a parameter centered which by default is TRUE. Actually basehaz() gives cumulative hazard H(t). See here. That is, exp(-basehaz(fit)$hazard) is the same as summary(survfit(fit))$surv. basehaz() function is not useful.

fit <- coxph(Surv(futime, fustat) ~ age, data = ovarian) 
> fit
Call:
coxph(formula = Surv(futime, fustat) ~ age, data = ovarian)

      coef exp(coef) se(coef)    z      p
age 0.1616    1.1754   0.0497 3.25 0.0012

Likelihood ratio test=14.3  on 1 df, p=0.000156
n= 26, number of events= 12 

# Note the default 'centered = TRUE' for basehaz() 
> exp(-basehaz(fit)$hazard) # exp(-cumulative hazard)
 [1] 0.9880206 0.9738738 0.9545899 0.9334790 0.8973620 0.8624781 0.8243117
 [8] 0.8243117 0.8243117 0.7750981 0.7750981 0.7244924 0.6734146 0.6734146
[15] 0.5962187 0.5204807 0.5204807 0.5204807 0.5204807 0.5204807 0.5204807
[22] 0.5204807 0.5204807 0.5204807 0.5204807 0.5204807
> dim(ovarian)
[1] 26  6
> exp(-basehaz(fit)$hazard)[ovarian$fustat == 1]
 [1] 0.9880206 0.9738738 0.9545899 0.8973620 0.8243117 0.8243117 0.7750981
 [8] 0.7750981 0.5204807 0.5204807 0.5204807 0.5204807
> summary(survfit(fit))$surv 
 [1] 0.9880206 0.9738738 0.9545899 0.9334790 0.8973620 0.8624781 0.8243117
 [8] 0.7750981 0.7244924 0.6734146 0.5962187 0.5204807
> summary(survfit(fit, data.frame(age=mean(ovarian$age))), 
          time=ovarian$futime[ovarian$fustat == 1])$surv
# Same result as above
> summary(survfit(fit, data.frame(age=mean(ovarian$age))), 
                    time=ovarian$futime)$surv
 [1] 0.9880206 0.9738738 0.9545899 0.9334790 0.8973620 0.8624781 0.8243117
 [8] 0.8243117 0.8243117 0.7750981 0.7750981 0.7244924 0.6734146 0.6734146
[15] 0.5962187 0.5204807 0.5204807 0.5204807 0.5204807 0.5204807 0.5204807
[22] 0.5204807 0.5204807 0.5204807 0.5204807 0.5204807

Calculating survival probability per person at time (t) from Cox PH

Predicted survival probability in Cox model: survfit.coxph(), plot.survfit() & summary.survfit( , times)

For theory, see section 8.6 Estimation of the survival function in Klein & Moeschberger. See the formula in Prediction in Cox regression.

For R, see Extract survival probabilities in Survfit by groups

plot.survfit(). fun="log" to plot log survival curve, fun="event" plot cumulative events, fun="cumhaz" plots cumulative hazard (f(y) = -log(y)).

The plot function below will draw 4 curves: [math]\displaystyle{ S_0(t)^{\exp(\hat{\beta}_{age}*60)} }[/math], [math]\displaystyle{ S_0(t)^{\exp(\hat{\beta}_{age}*60+\hat{\beta}_{stageII})} }[/math], [math]\displaystyle{ S_0(t)^{\exp(\hat{\beta}_{age}*60+\hat{\beta}_{stageIII})} }[/math], [math]\displaystyle{ S_0(t)^{\exp(\hat{\beta}_{age}*60+\hat{\beta}_{stageIV})} }[/math].

library(KMsurv) # Data package for Klein & Moeschberge
data(larynx)
larynx$stage <- factor(larynx$stage)
coxobj <- coxph(Surv(time, delta) ~ age + stage, data = larynx)

# Figure 8.3 from Section 8.6
plot(survfit(coxobj, newdata = data.frame(age=rep(60, 4), stage=factor(1:4))), lty = 1:4)

# Estimated probability for a 60-year old for different stage patients
out <- summary(survfit(coxobj, data.frame(age = rep(60, 4), stage=factor(1:4))), times = 5)
out$surv
#  time n.risk n.event survival1 survival2 survival3 survival4
#    5     34      40     0.702     0.665      0.51     0.142
sum(larynx$time >=5) # n.risk
# [1] 34
sum(larynx$delta[larynx$time <=5]) # n.event
# [1] 40
sum(larynx$time >5) # Wrong
# [1] 31
sum(larynx$delta[larynx$time <5]) # Wrong
# [1] 39

# 95% confidence interval
out$lower
# 0.8629482 0.9102532 0.7352413 0.548579
out$upper
# 0.5707952 0.4864903 0.3539527 0.03691768

We need to pay attention when the number of covariates is large (and we don't want to specify each covariates in the formula). The key is to create a data frame and use dot (.) in the formula. This is to fix a warning message: 'newdata' had XXX rows but variables found have YYY rows from running survfit(, newdata).

Another way is to use as.formula() if we don't want to create a new object.

xsub <- data.frame(xtrain)
colnames(xsub) <- paste0("x", 1:ncol(xsub))

coxobj <- coxph(Surv(ytrain[, "time"], ytrain[, "status"]) ~ ., data = xsub)

newdata <- data.frame(xtest)
colnames(newdata) <- paste0("x", 1:ncol(newdata))

survprob <- summary(survfit(coxobj, newdata=newdata), 
                    times = 5)$surv[1, ]  
# since there is only 1 time point, we select the first row in surv (surv is a matrix with one row).

The predictSurvProb() function from the pec package can also be used to extract survival probability predictions from various modeling approaches.

Visualizing the estimated distribution of survival times

survminer::ggsurvplot(); see here.

Predicted survival probabilities from glmnet: c060/peperr, biospear packages and manual computation

## S3 method for class 'glmnet'
predictProb(object, response, x, times, complexity, ...)

set.seed(1234)
junk <- biospear::simdata(n=500, p=500, q.main = 10, q.inter = 0, 
                  prob.tt = .5, m0=1, alpha.tt=0, 
                  beta.main= -.5, b.corr = .7, b.corr.by=25, 
                  wei.shape = 1, recr=3, fu=2, timefactor=1)
summary(junk$time)
library(glmnet)
library(c060) # Error: object 'predictProb' not found
library(peperr)

y <- cbind(time=junk$time, status=junk$status)
x <- cbind(1, junk[, "treat", drop = FALSE])
names(x) <- c("inter", "treat")
x <- as.matrix(x)
cvfit <- cv.glmnet(x, y, family = "cox")
obj <- glmnet(x, y, family = "cox")
xnew <- matrix(c(0,0), nr=1)
predictProb(obj, y, xnew, times=1, complexity = cvfit$lambda.min)
# Error in exp(lp[response[, 1] >= t.unique[i]]) : 
#   non-numeric argument to mathematical function
# In addition: Warning message:
# In is.na(x) : is.na() applied to non-(list or vector) of type 'NULL'

https://www.rdocumentation.org/packages/biospear/versions/1.0.1/topics/expSurv and manual computation (search bhaz)

expSurv(res, traindata, method, ci.level = .95, boot = FALSE, nboot, smooth = TRUE,
  pct.group = 4, time, trace = TRUE, ncores = 1)
# S3 method for resexpSurv
predict(object, newdata, ...)

# continue the example
# BMsel() takes a little while
resBM <- biospear::BMsel(
    data = junk, 
    method = "lasso", 
    inter = FALSE, 
    folds = 5)
  
# Note: if we specify time =5 in expsurv(), we will get an error message
# 'time' is out of the range of the observed survival time.
# Note: if we try to specify more than 1 time point, we will get the following msg
# 'time' must be an unique value; no two values are allowed.
esurv <- biospear::expSurv(
    res = resBM,
    traindata = junk,
    boot = FALSE,
    time = median(junk$time),
    trace = TRUE)
# debug(biospear:::plot.resexpSurv)
plot(esurv, method = "lasso")
# This is equivalent to doing the following
xx <- attributes(esurv)$m.score[, "lasso"]
wc <- order(xx); wgr <- 1:nrow(esurv$surv)
p1 <- plot(x = xx[wc], y = esurv$surv[wgr, "lasso"][wc], 
           xlab='prognostic score', ylab='survival prob')
# prognostic score beta*x in this cases.
# ignore treatment effect and interactions
xxmy <- as.vector(as.matrix(junk[, names(resBM$lasso)]) %*% resBM$lasso)
# See page4 of the paper. Scaled scores were used in the plot
range(abs(xx - (xxmy-quantile(xxmy, .025)) / (quantile(xxmy, .975) -  quantile(xxmy, .025))))
# [1] 1.500431e-09 1.465241e-06

h0 <- bhaz(resBM$lasso, junk$time, junk$status, junk[, names(resBM$lasso)])
newtime <- median(junk$time)
H0 <- sapply(newtime, function(tt) sum(h0$h[h0$dt <= tt]))
# newx <- junk[ , names(resBM$lasso)]
# Compute the estimate of the survival probability at training x and time = median(junk$time)
# using Breslow method
S2 <- outer(exp(-H0),  exp(xxmy), "^") # row = newtime, col = newx
range(abs(esurv$surv[wgr, "lasso"] - S2))
# [1] 6.455479e-18 2.459136e-06
# My implementation of the prognostic plot
#   Note that the x-axis on the plot is based on prognostic scores beta*x, 
#   not on treatment modifying scores gamma*x as described in the paper.
#   Maybe it is because inter = FALSE in BMsel() we have used.
p2 <- plot(xxmy[wc], S2[wc], xlab='prognostic score', ylab='survival prob')  # cf p1

> names(esurv)
[1] "surv"  "lower" "upper"
> str(esurv$surv)
 num [1:500, 1:2] 0.772 0.886 0.961 0.731 0.749 ...
 - attr(*, "dimnames")=List of 2
  ..$ : NULL
  ..$ : chr [1:2] "lasso" "oracle"

esurv2 <- predict(esurv, newdata = junk)
esurv2$surv       # All zeros?

Bug from the sample data (interaction was considered here; inter = TRUE) ?

set.seed(123456)
resBM <-  BMsel(
  data = Breast,
  x = 4:ncol(Breast),
  y = 2:1,
  tt = 3,
  inter = TRUE,
  std.x = TRUE,
  folds = 5,
  method = c("lasso", "lasso-pcvl"))

esurv <- expSurv(
  res = resBM,
  traindata = Breast,
  boot = FALSE,
  smooth = TRUE,
  time = 4,
  trace = TRUE
)
Computation of the expected survival
Computation of analytical confidence intervals
Computation of smoothed B-splines
Error in cobs(x = x, y = y, print.mesg = F, print.warn = F, method = "uniform",  : 
  There is at least one pair of adjacent knots that contains no observation.

Plot predictor vs HR

https://github.com/tjbencomo/survival-talk-pntlab/blob/master/survival_talk.pdf
https://www.imsbio.co.jp/RGM/R_rdfile?f=Greg/man/plotHR.Rd&d=R_CC which uses Greg::plotHR() function.
ggplot(Predict(modA_cph, age)) log relative hazard vs predictor

Loglikelihood

fit$loglik is a vector of length 2 (initial model, fitted model). So deviance can be calculated by -2*fit$loglik[2]; see here for an example from BhGLM package.
Use survival::anova() command to do a likelihood ratio test. Note this function does not work on glmnet object.
residuals.coxph Calculates martingale, deviance, score or Schoenfeld residuals for a Cox proportional hazards model.
No deviance() on coxph object!
logLik() function will return fit$loglik[2]
Gradient descent for the elastic net Cox-PH model

glmnet

It seems AIC does not require the assumption of nested models.
https://en.wikipedia.org/wiki/Akaike_information_criterion, (akaike pronunciation in Japanese)

[math]\displaystyle{ \begin{align} \mathrm{AIC} &= 2k - 2\ln(\hat L) \\ \mathrm{AICc} &= \mathrm{AIC} + \frac{2k^2 + 2k}{n - k - 1} \end{align} }[/math]

Is it possible to calculate AIC and BIC for lasso regression models?. See the references about the degrees of freedom in Lasso regressions.

fit <- glmnet(x, y, family = "multinomial") 

tLL <- fit$nulldev - deviance(fit) # ln(L)
k <- fit$df
n <- fit$nobs
AICc <- -tLL+2*k+2*k*(k+1)/(n-k-1)
AICc

https://github.com/nyiuab/BhGLM/blob/master/R/bmlasso.r#L143

f <- glmnet(x = x, y = y, family = family)
f$aic <- deviance(f) + 2 * f$df

For glmnet object, see ?deviance.glmnet, ?coxnet.deviance and R: Getting AIC/BIC/Likelihood from GLMNet. An example with all continuous variables

set.seed(10101)
N=1000;p=6
nzc=p/3
x=matrix(rnorm(N*p),N,p)
beta=rnorm(nzc)
fx=x[,seq(nzc)]%*%beta/3
hx=exp(fx)
ty=rexp(N,hx)
tcens=rbinom(n=N,prob=.3,size=1)# censoring indicator
y=cbind(time=ty,status=1-tcens) # y=Surv(ty,1-tcens) with library(survival)
coxobj <- coxph(Surv(ty, 1-tcens) ~ x)
coxobj_small <- coxph(Surv(ty, 1-tcens) ~1)
anova(coxobj, coxobj_small)
# Analysis of Deviance Table
# Cox model: response is  Surv(ty, 1 - tcens)
# Model 1: ~ x
# Model 2: ~ 1
# loglik  Chisq Df P(>|Chi|)  
# 1 -4095.2                      
# 2 -4102.7 15.151  6   0.01911 *

fit2 <- glmnet(x,y,family="cox", lambda=0) # ridge regression
deviance(fit2)                             # 2*(loglike_sat - loglike)
# [1] 8190.313
coxnet.deviance(x=x, y=y, beta=coef(fit2)) # 2*(loglike_sat - loglike)
# [1] 8190.313   
# https://github.com/cran/glmnet/blob/master/R/coxnet.deviance.R#L79

assess.glmnet(fit2, x=x, y=y)      # returns deviance and c-index
fit2$df
# [1] 6
fit2$nulldev - deviance(fit2) # Log-Likelihood ratio statistic
# [1] 15.15097
1-pchisq(fit2$nulldev - deviance(fit2), fit2$df)
# [1] 0.01911446

Here is another example including a factor covariate:

library(KMsurv) # Data package for Klein & Moeschberge
data(larynx)
larynx$stage <- factor(larynx$stage)
coxobj <- coxph(Surv(time, delta) ~ age + stage, data = larynx)
coef(coxobj)
# age    stage2    stage3    stage4 
# 0.0190311 0.1400402 0.6423817 1.7059796
coxobj_small <- coxph(Surv(time, delta)~age, data = larynx)
anova(coxobj, coxobj_small)
# Analysis of Deviance Table
# Cox model: response is  Surv(time, delta)
# Model 1: ~ age + stage
# Model 2: ~ age
# loglik  Chisq Df P(>|Chi|)   
# 1 -187.71                       
# 2 -195.55 15.681  3  0.001318 **
#   ---
#   Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1

# Now let's look at the glmnet() function.
# It seems glmnet does not recognize factor covariates.
coxobj2 <- with(larynx, glmnet(cbind(age, stage), Surv(time, delta), family = "cox", lambda=0))
coxobj2$nulldev - deviance(coxobj2)  # Log-Likelihood ratio statistic
# [1] 15.72596
coxobj1 <- with(larynx, glmnet(cbind(1, age), Surv(time, delta), family = "cox", lambda=0))
deviance(coxobj1) - deviance(coxobj2) 
# [1] 13.08457
1-pchisq(deviance(coxobj1) - deviance(coxobj2) , coxobj2$df-coxobj1$df)
# [1] 0.0002977376

High dimensional data

glmnet + Cox models

Robust estimation of the expected survival probabilities from high-dimensional Cox models with biomarker-by-treatment interactions in randomized clinical trials by Nils Ternès, Federico Rotolo and Stefan Michiels, BMC Medical Research Methodology, 2017 (open review available). The corresponding software biospear on cran and rdocumentation.org.
Accounting for grouped predictor variables or pathways in high-dimensional penalized Cox regression models Belhechmi 2020
Cancer prognosis prediction using somatic point mutation and copy number variation data: a comparison of gene-level and pathway-based models Zheng 2020
Expected time of survival in glmnet for cox family

Error in glmnet: x should be a matrix with 2 or more columns

https://stackoverflow.com/questions/29231123/why-cant-pass-only-1-coulmn-to-glmnet-when-it-is-possible-in-glm-function-in-r

Error in coxnet: (list) object cannot be coerced to type 'double'

Fix: do not use data.frame in X. Use cbind() instead.

Prediction

Prognostic factor, prognosis

"Prognostic" refers to the ability to predict the likely outcome or course of a disease. In the context of medicine, prognosis is the prediction of the future course of a disease and the chances of recovery or survival. A prognosis can be based on a variety of factors, including the stage and grade of the disease, the patient's overall health, and the response to treatment.
Prognostic factors are the characteristics of a patient or a disease that can be used to predict the outcome or course of the disease. These factors can include demographic information (such as age and gender), clinical information (such as the stage and grade of the disease), and laboratory test results.
Prognostic factors are used to stratify patients into different prognostic groups, which can help guide treatment decisions and identify patients who may be at high risk for poor outcomes. For example, in cancer treatment, the stage of the cancer, the location of the cancer, and the patient's overall health are important prognostic factors that are used to determine the best course of treatment.
It's worth noting that prognosis is not always certain, and unexpected events can happen that can change the course of the disease. Additionally, the effectiveness of treatment can change the prognosis for a patient. Prognosis is an estimation and it can change over time.
Prognosis. Grade I carcinomas tend to have be less aggressive and have a better prognosis than higher grade carcinomas. They are also more often ER positive, which is another feature associated with a more favorable prognosis. STAGING & GRADE breast cancer.

Prognostic index/risk scores

International Prognostic Index
In R,
- coxph() defines risk score as exp(linear predictor).
- survC1 package defines risk score as coxph's linear predictor; see his paper on Stat in Med 2011. Some medical papers (such as this one) also defines it in this way.
Low scores correspond to the lowest predicted risk and high scores correspond to the greatest predicted risk.
The test data were first segregated into high-risk and low-risk groups by the median of training risk scores. Assessment of performance of survival prediction models for cancer prognosis
On the paper "The C-index is not proper for the evaluation of t-year predicted risk" Blanche et al 2018 defined the true t-year predicted risk by [math]\displaystyle{ P(T \le t | Z) = 1 - Survival }[/math]

linear.predictors component in coxph object

The $linear.predictors component is not [math]\displaystyle{ \beta' x }[/math]. It is [math]\displaystyle{ \beta' (x-\mu_x) }[/math]. See this post.

predict.coxph, prognostic index & risk score

predict.coxph() Compute fitted values and regression terms for a model fitted by coxph. The Cox model is a relative risk model; predictions of type "linear predictor", "risk", and "terms" are all relative to the sample from which they came. By default, the reference value for each of these is the mean covariate within strata. The primary underlying reason is statistical: a Cox model only predicts relative risks between pairs of subjects within the same strata, and hence the addition of a constant to any covariate, either overall or only within a particular stratum, has no effect on the fitted results. Returned value: a vector or matrix of predictions, or a list containing the predictions (element "fit") and their standard errors (element "se.fit") if the se.fit option is TRUE.

predict(object, newdata,
    type=c("lp", "risk", "expected", "terms", "survival"),
    se.fit=FALSE, na.action=na.pass, terms=names(object$assign), collapse,
    reference=c("strata", "sample"),  ...)

type:

- "lp": linear predictor
- "risk": risk score exp(lp)
- "expected": the expected number of events given the covariates and follow-up time. The survival probability for a subject is equal to exp(-expected).
- "terms": the terms of the linear predictor.
http://stats.stackexchange.com/questions/44896/how-to-interpret-the-output-of-predict-coxph. The $linear.predictors component represents [math]\displaystyle{ \beta (x - \bar{x}) }[/math]. The risk score (type='risk') corresponds to [math]\displaystyle{ \exp(\beta (x-\bar{x})) }[/math]. Factors are converted to dummy predictors as usual; see model.matrix.
http://www.togaware.com/datamining/survivor/Lung1.html

library(coxph)
fit <- coxph(Surv(time, status) ~ age , lung)
fit
#  Call:
#  coxph(formula = Surv(time, status) ~ age, data = lung)
#       coef exp(coef) se(coef)    z     p
# age 0.0187      1.02   0.0092 2.03 0.042
#
# Likelihood ratio test=4.24  on 1 df, p=0.0395  n= 228, number of events= 165 
fit$means
#      age 
# 62.44737 

# type = "lr" (Linear predictor)
as.numeric(predict(fit,type="lp"))[1:10]   
# [1]  0.21626733  0.10394626 -0.12069589 -0.10197571 -0.04581518  0.21626733
# [7]  0.10394626  0.16010680 -0.17685643 -0.02709500
0.0187 * (lung$age[1:10] - fit$means)
# [1]  0.21603421  0.10383421 -0.12056579 -0.10186579 -0.04576579  0.21603421
# [7]  0.10383421  0.15993421 -0.17666579 -0.02706579
fit$linear.predictors[1:10]
# [1]  0.21626733  0.10394626 -0.12069589 -0.10197571 -0.04581518
# [6]  0.21626733  0.10394626  0.16010680 -0.17685643 -0.02709500

# type = "risk" (Risk score)
> as.numeric(predict(fit,type="risk"))[1:10]
 [1] 1.2414342 1.1095408 0.8863035 0.9030515 0.9552185 1.2414342 1.1095408
 [8] 1.1736362 0.8379001 0.9732688
> exp((lung$age-mean(lung$age)) * 0.0187)[1:10]
 [1] 1.2411448 1.1094165 0.8864188 0.9031508 0.9552657 1.2411448
 [7] 1.1094165 1.1734337 0.8380598 0.9732972
> exp(fit$linear.predictors)[1:10]
 [1] 1.2414342 1.1095408 0.8863035 0.9030515 0.9552185 1.2414342
 [7] 1.1095408 1.1736362 0.8379001 0.9732688

threshold/cutoff

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882539/ An optimal threshold on the score to separate patients into low- and high-risk groups was determined using the MaxStat package to select the cutoff value producing the maximal log-rank score in the training cohort.
maxstat: Maximally Selected Rank Statistics (cf the matrixStats: Functions that Apply to Rows and Columns of Matrices (and to Vectors) package).

Survival risk prediction

Using cross-validation to evaluate predictive accuracy of survival risk classifiers based on high-dimensional data Simon 2011. The authors have noted the CV has been used for optimization of tuning parameters but the data available are too limited for effective into training & test sets.
- The CV Kaplan-Meier curves are essentially unbiased and the separation between the curves gives a fair representation of the value of the expression profiles for predicting survival risk.
- The log-rank statistic does not have the usual chi-squared distribution under the null hypothesis. This is because the data was used to create the risk groups.
- Survival ROC curve can be used as a measure of predictive accuracy for the survival risk group model at a certain landmark time.
- The ROC curve can be misleading. For example if re-substitution is used, the AUC can be very large.
- The p-value for the significance of the test that AUC=.5 for the cross-validated survival ROC curve can be computed by permutations.
- Cross-validated estimates of survival risk discrimination can be pessimistically biased if the number of folds K is too small for the number of events, and the variance of the cross-validated risk group survival curves or time-dependent ROC curves will be large, particularly when K is large and the number of events is small. For example, for the null simulations of Figure 3, there are several cases in which the cross-validated Kaplan–Meier curve for the low-risk group is below that for the high-risk group.
- (class data) For small sample sizes of fewer than 50 cases, they recommended use of leave-one-out cross-validation to minimize mean squared error of the estimate of prediction error.
- (survival data) Subramanian and Simon (Stat Med) recommended use of 5- or 10-fold cross-validation for a wide range of conditions.
- Fig 1: KM substitution. 10 null data.
- Fig 2: KM test data. 10 null data.
- Fig 3: KM 10-fold CV. One null data.
- Fig 4A: KM Shedden data resubstitution.
- Fig 4B: KM Shedden data. CV
- Fig 5A: Resubstitution time-dep ROC. Shedden.
- Fig 5B: CV time-dep ROC. Shedden.
- Fig 6A: KM clinical covariates only
- Fig 6B: KM combined
- Fig 7. Time-dep ROC from covariates only and combined.
Some cites: Automated identification of stratifying signatures incellular subpopulations Tibshirani 2014.
Measure of assessment for prognostic prediction

	0/1	Survival
Sensitivity	[math]\displaystyle{ P(Pred=1\|True=1) }[/math]	[math]\displaystyle{ P(\beta' X \gt c \| T \lt t) }[/math]
Specificity	[math]\displaystyle{ P(Pred=0\|True=0) }[/math]	[math]\displaystyle{ P(\beta' X \le c \| T \ge t) }[/math]

An evaluation of resampling methods for assessment of survival risk prediction in high-dimensional settings Subramanian, et al 2010.
- The conditional probabilities can be estimated by Heagerty et al 2000 (R package survivalROC). The AUC(t) can be used for comparing and assessing prognostic models (a measure of accuracy) for future samples. In the absence of an independent large dataset, an estimate for AUC(t) is obtained through resampling from the original sample [math]\displaystyle{ S_n }[/math].
- Resubstitution estimate of AUC(t) (i.e. all observations were used for feature selection, model building as well as the estimation of accuracy) is too optimistic. So k-fold CV method is considered.
- There are two ways to compute k-fold CV estimate of AUC(t): the pooling strategy (used in the paper) and average strategy (AUC(t)s are first computed for each test set and are then averaged). In the pooling strategy, all the test set risk-score predictions are first collected and AUC(t) is calculated on this combined set.
- Conclusions: sample splitting and LOOCV have a higher mean square error than other methods. 5-fold or 10-fold CV provide a good balance between bias and variability for a wide range of data settings.
*Gene Expression–Based Prognostic Signatures in Lung Cancer: Ready for Clinical Use? Subramanian, et al 2010.
Assessment of survival prediction models based on microarray data Martin Schumacher, et al. 2007
Semi-Supervised Methods to Predict Patient Survival from Gene Expression Data Eric Bair , Robert Tibshirani, 2004
Time dependent ROC curves for censored survival data and a diagnostic marker. Heagerty et al, Biometrics 2000
- An introduction to survivalROC by Saha, Heagerty. If the AUCs are computed at several time points, we can plot the AUCs vs time for different models (eg different covariates) and compare them to see which model performs better.
- The survivalROC package does not draw an ROC curve. It outputs FP (x-axis) and TP (y-axis). We can use basic R or ggplot to draw the curve.
- survivalROC() calculates AUC at specified time by using NNE method (default). We can use the prognostic index as marker when there are more than one markers is used. Note that survAUC::AUC.uno() uses Uno (2007) to calculate FP and TP.
- Assessment of Discrimination in Survival Analysis (C-statistics, etc)
- plotROC package by Sachs for showing ROC curves from multiple time points on the same plot.
- Time-dependent ROC for Survival Prediction Models in R. It shows the effect of the number of events and the selection of predict time. It also emphasized the survivalROC package implements the cumulative case/dynamic control ROC and the risksetROC package implements the incident case/dynamic control ROC.
- survivalROC怎么看最佳cut-off值？/ HOW to use the survivalROC to get optimal cut-off values? 最优的点应该就是斜率等于1的地方.
Survival prediction from clinico-genomic models - a comparative study Hege M Bøvelstad, 2009
Assessment and comparison of prognostic classification schemes for survival data. E. Graf, C. Schmoor, W. Sauerbrei, et al. 1999
What do we mean by validating a prognostic model? Douglas G. Altman, Patrick Royston, 2000
On the prognostic value of survival models with application to gene expression signatures T. Hielscher, M. Zucknick, W. Werft, A. Benner, 2000
Accuracy of point predictions in survival analysis, Henderson et al, Statist Med, 2001.
Assessment of performance of survival prediction models for cancer prognosis Hung-Chia Chen et al 2012
Accuracy of predictive ability measures for survival models Flandre, Detsch and O'Quigley, 2017.
Association between expression of random gene sets and survival is evident in multiple cancer types and may be explained by sub-classification Yishai Shimoni, PLOS 2018
Development and validation of risk prediction equations to estimate survival in patients with colorectal cancer: cohort study
Cox-nnet: An artificial neural network method for prognosis prediction of high-throughput omics data Ching et al 2018.
A scoping methodological review of simulation studies comparing statistical and machine learning approaches to risk prediction for time-to-event data Smith, 2022

Survival time prediction

Survival time prediction by integrating cox proportional hazards network and distribution function network Baek 2021

Assessing the performance of prediction models

Investigating the prediction ability of survival models based on both clinical and omics data: two case studies by Riccardo De Bin, Statistics in Medicine 2014. (not useful)
Assessment of performance of survival prediction models for cancer prognosis Chen et al , BMC Medical Research Methodology 2012
A simulation study of predictive ability measures in a survival model I: Explained variation measures Choodari‐Oskooei et al, Stat in Medicine 2011
Assessing the performance of prediction models: a framework for some traditional and novel measures by Ewout W. Steyerberg, Andrew J. Vickers, [...], and Michael W. Kattan, 2010.
survcomp: an R/Bioconductor package for performance assessment and comparison of survival models paper in 2011 and Introduction to R and Bioconductor Survival analysis where the survcomp package can be used. The summary here is based on this paper.
- concordance.index(). Pencina, M. J. and D'Agostino, R. B. (2004) "Overall C as a measure of discrimination in survival analysis: model specific population value and confidence interval estimation", Statistics in Medicine, 23, pages 2109–2123, 2004.
How to compare predictive power of survival models?
How to compare Harrell C-index from different models in survival analysis? and Frank Harrell's comment: Doing model comparison with LR statistics is more powerful than using methods that depend on an asymptotic distribution of the C-index.
Assessing performance and clinical usefulness in prediction models with survival outcomes: practical guidance for Cox proportional hazards models 2022. Source code.

Hazard ratio

hazard.ratio()

hazard.ratio(x, surv.time, surv.event, weights, strat, alpha = 0.05, 
             method.test = c("logrank", "likelihood.ratio", "wald"), na.rm = FALSE, ...)

Odds ratio 優勢比/比值比/發生比

RR值、OR值、HR值：临床研究中的3个“R”你都分清了吗?. 相对危险度RR（relative risk）、风险比HR（hazard ratio）、比值比OR（odds ratio）
医学统计学中RR、OR和HR三个关于比值的概念
發生比 Odds, https://en.wikipedia.org/wiki/Odds_ratio has relative risk and odds ratio.
Limitations of the Odds Ratio in Gauging the Performance of a Diagnostic, Prognostic, or Screening Marker Pepe 2004. C statistic measures discrimination ability better than relative risk does; see this paper.

D index

D.index()

D.index(x, surv.time, surv.event, weights, strat, alpha = 0.05, 
        method.test = c("logrank", "likelihood.ratio", "wald"), na.rm = FALSE, ...)

AUC

See ROC curve.

Comparison:

	Definition	Interpretation
Two class	[math]\displaystyle{ P(Z_{case} \gt Z_{control}) }[/math]	the probability that a randomly selected case will have a higher test result (marker value) than a randomly selected control. It represents a measure of concordance between the marker and the disease status. ROC curves are particularly useful for comparing the discriminatory capacity of different potential biomarkers. (Heagerty & Zheng 2005)
Survival data	[math]\displaystyle{ P(\beta' Z_1 \gt \beta' Z_2\|T_1 \lt T_2) }[/math]	(Roughly speaking) the probability of concordance between predicted and observed responses. The probability that the predictions for a random pair of subjects are concordant with their outcomes. (Heagerty & Zheng 2005). (Precisely) fraction of pairs in your data, where the observation with the higher survival time has the higher probability of survival predicted by your model.

p95 of Heagerty and Zheng (2005) gave a relationship of C-statistic:

[math]\displaystyle{ C = P(M_j \gt M_k | T_j \lt T_k) = \int_t \mbox{AUC(t) w(t)} \; dt }[/math]

where M is the marker value and [math]\displaystyle{ w(t) = 2 \cdot f(t) \cdot S(t) }[/math]. When the interest is in the accuracy of a regression model we will use [math]\displaystyle{ M_i = Z_i^T \beta }[/math].

The time-dependent AUC is also related to time-dependent C-index. [math]\displaystyle{ C_\tau = P(M_j \gt M_k | T_j \lt T_k, T_j \lt \tau) = \int_t \mbox{AUC(t)} \mbox{w}_{\tau}(t) \; dt }[/math] where [math]\displaystyle{ w_\tau(t) = 2 \cdot f(t) \cdot S(t)/(1-S^2(\tau)) }[/math].

Integrated brier score (≈ "mean squared error" of prediction for survival data)

Assessment and comparison of prognostic classification schemes for survival data Graf et al Stat. Med. 1999 2529-45, Consistent Estimation of the Expected Brier Score in General Survival Models with Right‐Censored Event Times Gerds et al 2006.

Because the point predictions of event-free times will almost inevitably given inaccurate and unsatisfactory result, the mean square error of prediction [math]\displaystyle{ \frac{1}{n}\sum_1^n (T_i - \hat{T}(X_i))^2 }[/math] method will not be considered. See Parkes 1972 or Henderson 2001.
Another approach is to predict the survival or event status [math]\displaystyle{ Y=I(T \gt \tau) }[/math] at a fixed time point [math]\displaystyle{ \tau }[/math] for a patient with X=x. This leads to the expected Brier score [math]\displaystyle{ E[(Y - \hat{S}(\tau|X))^2] }[/math] where [math]\displaystyle{ \hat{S}(\tau|X) }[/math] is the estimated event-free probabilities (survival probability) at time [math]\displaystyle{ \tau }[/math] for subject with predictor variable [math]\displaystyle{ X }[/math].
The time-dependent Brier score (without censoring)

[math]\displaystyle{ \begin{align} \mbox{Brier}(\tau) &= \frac{1}{n}\sum_1^n (I(T_i\gt \tau) - \hat{S}(\tau|X_i))^2 \end{align} }[/math]

The time-dependent Brier score (with censoring, C is the censoring variable)

[math]\displaystyle{ \begin{align} \mbox{Brier}(\tau) = \frac{1}{n}\sum_i^n\bigg[\frac{(\hat{S}_C(t_i))^2I(t_i \leq \tau, \delta_i=1)}{\hat{S}_C(t_i)} + \frac{(1 - \hat{S}_C(t_i))^2 I(t_i \gt \tau)}{\hat{S}_C(\tau)}\bigg] \end{align} }[/math]

where [math]\displaystyle{ \hat{S}_C(t_i) = P(C \gt t_i) }[/math], the Kaplan-Meier estimate of the censoring distribution with [math]\displaystyle{ t_i }[/math] the survival time of patient i. The integration of the Brier score can be done by over time [math]\displaystyle{ t \in [0, \tau] }[/math] with respect to some weight function W(t) for which a natual choice is [math]\displaystyle{ (1 - \hat{S}(t))/(1-\hat{S}(\tau)) }[/math]. The lower the iBrier score, the larger the prediction accuracy is.

Useful benchmark values for the Brier score are 33%, which corresponds to predicting the risk by a random number drawn from U[0, 1], and 25% which corresponds to predicting 50% risk for everyone. See Evaluating Random Forests for Survival Analysis using Prediction Error Curves by Mogensen et al J. Stat Software 2012 (pec package). The paper has a good summary of different R package implementing Brier scores.

R function

pec by Thomas A. Gerds. The plot.pec() can plot prediction error curves (defined by Brier score). See an example from this paper. The .632+ bootstrap prediction error curves is from the paper Boosting for high-dimensional time-to-event data with competing risks 2009
peperr package. The package peperr is an early branch of pec.
survcomp::sbrier.score2proba().
ipred::sbrier()

Papers on high dimensional covariates

Assessment of survival prediction models based on microarray data, Bioinformatics , 2007, vol. 23 (pg. 1768-74)
Allowing for mandatory covariates in boosting estimation of sparse high-dimensional survival models, BMC Bioinformatics , 2008, vol. 9 pg. 14

Kendall's tau, Goodman-Kruskal's gamma, Somers' d

https://en.wikipedia.org/wiki/Kendall_rank_correlation_coefficient
https://en.wikipedia.org/wiki/Goodman_and_Kruskal%27s_gamma
https://en.wikipedia.org/wiki/Somers%27_D
Survival package has a good summary. Especially concordance = (d+1)/2.

Concordance index/C-index/C-statistic interpretation and R packages

Pitfalls of the concordance index for survival outcomes Hartman 2023
The area under ROC curve (plot of sensitivity of 1-specificity) is also called C-statistic. It is a measure of discrimination generalized for survival data (Harrell 1982 & 2001). The ROC are functions of the sensitivity and specificity for each value of the measure of model. (Nancy Cook, 2007)
- The sensitivity of a test is the probability of a positive test result, or of a value above a threshold, among those with disease (cases).
- The specificity of a test is the probability of a negative test result, or of a value below a threshold, among those without disease (noncases).
- Perfect discrimination corresponds to a c-statistic of 1 & is achieved if the scores for all the cases are higher than those for all the non-cases.
- The c-statistic is the probability that the measure or predicted risk/risk score is higher for a case than for a noncase.
- The c-statistic is not the probability that individuals are classified correctly or that a person with a high test score will eventually become a case.
- C-statistic is a rank-based measure. The c-statistic describes how well models can rank order cases and noncases, but not a function of the actual predicted probabilities.
How to interpret the output for calculating concordance index (c-index)? [math]\displaystyle{ P(\beta' Z_1 \gt \beta' Z_2|T_1 \lt T_2) }[/math] where T is the survival time and Z is the covariates.
- It is the fraction of pairs in your data, where the observation with the higher survival time has the higher probability of survival predicted by your model.
- High values mean that your model predicts higher probabilities of survival for higher observed survival times.
- The c index estimates the probability of concordance between predicted and observed responses. A value of 0.5 indicates no predictive discrimination and a value of 1.0 indicates perfect separation of patients with different outcomes. (p371 Harrell 1996)
Drawback of C-statistics:
- Even though rank indexes such as c are widely applicable and easily interpretable, they are not sensitive for detecting small differences in discrimination ability between two models. This is due to the fact that a rank method considers the (prediction, outcome) pairs (0.01,0), (0.9, 1) as no more concordant than the pairs (0.05,0), (0.8, 1). A more sensitive likelihood-ratio Chi-square-based statistic that reduces to R2 in the linear regression case may be substituted. (p371 Harrell 1996)
- If the model is correct, the likelihood based measures may be more sensitive in detecting differences in prediction ability, compared to rank-based measures such as C-indexes. (Uno 2011 p 1113)
What is Harrell’s C-index? C = #concordant pairs / (# concordant pairs + # discordant pairs)
http://dmkd.cs.vt.edu/TUTORIAL/Survival/Slides.pdf
Concordance vignette from the survival package. It has a good summary of different ways (such as Kendall's tau and Somers' d) to calculate the concordance statistic. The concordance function in the survival package can be used with various types of models including logistic and linear regression.
Assessment of Discrimination in Survival Analysis (C-statistics, etc) webpage
5 Ways to Estimate Concordance Index for Cox Models in R, Why Results Aren't Identical?, 计算的5种不同方法及比较. The 5 functions are rcorrcens() from Hmisc, summary()$concordance from survival, survConcordance() from survival, concordance.index() from survcomp and cph() from rms.
- The timewt option in survival::concordance() function is only applicable to censored data. In this case the default corresponds to Harrell's C statistic, which is closely related to the Gehan-Wilcoxon test; timewt="S" corrsponds to the Peto-Wilcoxon, timewt="S/G" is suggested by Schemper, and timewt="n/G2" corresponds to Uno's C.
- Uno’s C-statistic, which is implemented in the UnoC() function in the survAUC package in R, is a censoring-adjusted concordance statistic. It is based on inverse-probability-of-censoring weights. The inverse-probability-of-censoring weights adjust for the fact that censored observations contribute less information to the concordance statistic than uncensored observations. This adjustment helps to reduce bias in the concordance statistic due to censoring. How these weights are applied: 1. For each observation in the dataset, calculate the probability of being censored at each time point (The probability of being censored at each time point can then be estimated as one minus the survival function at that time point). 2. Take the inverse of these probabilities to get the weights. 3. Apply these weights when calculating the concordance statistic.

Summary of R packages to compute C-statistic

Package	Function	New data?	Comparison
survival	summary(coxph(formula, data))$concordance["C"], Cindex()	no, yes	no
survC1	Est.Cval()	no	Inf.Cval.Delta(, , , tau)
survAUC	UnoC()	yes	no
survivalROC	survivalROC()	no	no
timeROC	?	?	compare()
compareC	?	?	compareC()
survcomp	concordance.index()	?	cindex.comp()
Hmisc	rcorr.cens()	no	no
pec	cindex()	yes	see ?cindex doc with splitMethod parameter Note it requires time t See the warning C-stat eval at t is not proper

C-statistics

For two groups data (one with event, one without), C-statistic has an intuitive interpretation: if two individuals are selected at random, one with the event and one without, then the C-statistic is the probability that the model predicts a higher risk for the individual with the event. Analysis of Biomarker Data: logs, odds ratios and ROC curves by Grund 2010
C-statistics is the probability of concordance between predicted and observed survival.
Comparing two correlated C indices with right‐censored survival outcome: a one‐shot nonparametric approach Kang et al, Stat in Med, 2014. compareC package for comparing two correlated C-indices with right censored outcomes. Harrell’s Concordance. The s.e. of the Harrell's C-statistics can be estimated by the delta method. [math]\displaystyle{ \begin{align} C_H = \frac{\sum_{i,j}I(t_i \lt t_{j}) I(\hat{\beta} Z_i \gt \hat{\beta} Z_j) \delta_i}{\sum_{i,j} I(t_i \lt t_j) \delta_i} \end{align} }[/math] converges to a censoring-dependent quantity [math]\displaystyle{ P(\beta'Z_1 \gt \beta' Z_2|T_1 \lt T_2, T_1 \lt \text{min}(D_1,D_2)). }[/math] Here D is the censoring variable.
On the C-statistics for Evaluating Overall Adequacy of Risk Prediction Procedures with Censored Survival Data by Uno et al 2011. Let [math]\displaystyle{ \tau }[/math] be a specified time point within the support of the censoring variable. [math]\displaystyle{ \begin{align} C(\tau) = \text{UnoC}(\hat{\pi}, \tau) = \frac{\sum_{i,i'}(\hat{S}_C(t_i))^{-2}I(t_i \lt t_{i'}, t_i \lt \tau) I(\hat{\beta}'Z_i \gt \hat{\beta}'Z_{i'}) \delta_i}{\sum_{i,i'}(\hat{S}_C(t_i))^{-2}I(t_i \lt t_{i'}, t_i \lt \tau) \delta_i} \end{align} }[/math], a measure of the concordance between [math]\displaystyle{ \hat{\beta} Z_i }[/math] (the linear predictor) and the survival time. [math]\displaystyle{ \hat{S}_C(t) }[/math] is the Kaplan-Meier estimator for the censoring distribution/variable/time (cf event time); flipping the definition of [math]\displaystyle{ \delta_i }[/math]/considering failure events as "censored" observations and censored observations as "failures" and computing the KM as usual; see p207 of Satten 2001 and the source code from the kmcens() in survC1. Note that [math]\displaystyle{ C_\tau }[/math] converges to [math]\displaystyle{ P(\beta'Z_1 \gt \beta' Z_2|T_1 \lt T_2, T_1 \lt \tau). }[/math]
- Uno's estimator does not require the fitted model to be correct . See also table V in the simulation study where the true model is log-normal regression.
- Uno's estimator is consistent for a population concordance measure that is free of censoring. See the coverage result in table IV and V from his simulation study. Other forms of C-statistic estimate population parameters that may depend on the current study-specific censoring distribution.
- To accommodate discrete risk scores, in survC1::Est.Cval(), it is using the formula [math]\displaystyle{ . \begin{align} \frac{\sum_{i,i'}[ (\hat{S}_C(t_i))^{-2}I(t_i \lt t_{i'}, t_i \lt \tau) I(\hat{\beta}'Z_i \gt \hat{\beta}'Z_{i'}) \delta_i + 0.5 * (\hat{S}_C(t_i))^{-2}I(t_i \lt t_{i'}, t_i \lt \tau) I(\hat{\beta}'Z_i = \hat{\beta}'Z_{i'}) \delta_i ]}{\sum_{i,i'}(\hat{S}_C(t_i))^{-2}I(t_i \lt t_{i'}, t_i \lt \tau) \delta_i} \end{align} }[/math]. Note that pec::cindex() is using the same formula but survAUC::UnoC() does not.
- If the specified [math]\displaystyle{ \tau }[/math] (tau) is 'too' large such that very few events were observed or very few subjects were followed beyond this time point, the standard error estimate for [math]\displaystyle{ \hat{C}_\tau }[/math] can be quite large.
- Uno mentioned from (page 95) Heagerty and Zheng 2005 that when T is right censoring, one would typically consider [math]\displaystyle{ C_\tau }[/math] with a fixed, prespecified follow-up period [math]\displaystyle{ (0, \tau) }[/math].
- Uno also mentioned that when the data is right censored, the censoring variable D is usually shorter than that of the failure time T, the tail part of the estimated survival function of T is rather unstable. Thus we consider a truncated version of C.
- Heagerty and Zheng (2005) p95 said [math]\displaystyle{ C_\tau }[/math] is the probability that the predictions for a random pair of subjects are concordant with their outcomes, given that the smaller event time occurs in [math]\displaystyle{ (0, \tau) }[/math].
- real data 1: fit a Cox model. Get risk scores [math]\displaystyle{ \hat{\beta}'Z }[/math]. Compute the point and confidence interval estimates (M=500 indep. random samples with the same sample size as the observation data) of [math]\displaystyle{ C_\tau }[/math] for different [math]\displaystyle{ \tau }[/math]. Compare them with the conventional C-index procedure (Korn).
- real data 1: compute [math]\displaystyle{ C_\tau }[/math] for a full model and a reduce model. Compute the difference of them ([math]\displaystyle{ C_\tau^{(A)} - C_\tau^{(B)} = .01 }[/math]) and the 95% confidence interval (-0.00, .02) of the difference for testing the importance of some variable (HDL in this case). Though HDL is quite significant (p=0) with respect to the risk of CV disease but its incremental value evaluated via C-statistics is quite modest.
- real data 2: goal - evaluate the prognostic value of a new gene signature in predicting the time to death or metastasis for breast cancer patients. Two models were fitted; one with age+ER and the other is gene+age+ER. For each model we can calculate the point and interval estimates of [math]\displaystyle{ C_\tau }[/math] for different [math]\displaystyle{ \tau }[/math]s.
- simulation: T is from Weibull regression for case 1 and log-normal regression for case 2. Covariates = (age, ER, gene). 3 kinds of censoring were considered. Sample size is 100, 150, 200 and 300. 1000 iterations. Compute coverage probabilities and average length of 95% confidence intervals, bias and root mean square error for [math]\displaystyle{ \tau }[/math] equals to 10 and 15. Compared with the conventional approach, the new method has higher coverage probabilities and less bias in 6 scenarios.
Statistical methods for the assessment of prognostic biomarkers (Part I): Discrimination by Tripep et al 2010

Gonen and Heller 2005 concordance index for Cox models

[math]\displaystyle{ P(T_2\gt T_1|g(Z_1)\gt g(Z_2)) }[/math]. Gonen and Heller's c statistic which is independent of censoring.
GHCI() from survAUC package. Strangely only one parameter is needed. survAUC allows for testing data but CPE package does not have an option for testing data.

TR <- ovarian[1:16,]
TE <- ovarian[17:26,]
train.fit  <- coxph(Surv(futime, fustat) ~ age,
                    x=TRUE, y=TRUE, method="breslow", data=TR)
lpnew <- predict(train.fit, newdata=TE)      
survAUC::GHCI(lpnew) # .8515

lpnew2 <- predict(train.fit, newdata = TR)
survAUC::GHCI(lpnew2) # 0.8079495

CPE::phcpe(train.fit, CPE.SE = TRUE) 
# $CPE
# [1] 0.8079495
# $CPE.SE
# [1] 0.0670646

Hmisc::rcorr.cens(-TR$age, Surv(TR$futime, TR$fustat))["C Index"]
# 0.7654321 
Hmisc::rcorr.cens(TR$age, Surv(TR$futime, TR$fustat))["C Index"]
# 0.2345679

Used by simulatorZ package

Uno's C-statistics (2011) and some examples using different packages

C-statistic may or may not be a decreasing function of tau. However, AUC(t) may not be decreasing; see Fig 1 of Blanche et al 2018.

library(survAUC); library(pec)
set.seed(1234)
dat <- simulWeib(N=100, lambda=0.01, rho=1, beta=-0.6, rateC=0.001) # simulWebib was defined above
#     coef exp(coef) se(coef)     z      p
# x -0.744     0.475    0.269 -2.76 0.0057
TR <- dat[1:80,]
TE <- dat[81:100,]
train.fit  <- coxph(Surv(time, status) ~ x, data=TR)
plot(survfit(Surv(time, status) ~ 1, data =TR))

lpnew <- predict(train.fit, newdata=TE)
Surv.rsp <- Surv(TR$time, TR$status)
Surv.rsp.new <- Surv(TE$time, TE$status)              
sapply(c(.25, .5, .75),
       function(qtl) UnoC(Surv.rsp, Surv.rsp.new, lpnew, time=quantile(TR$time, qtl)))
# [1] 0.2580193 0.2735142 0.2658271
sapply(c(.25, .5, .75), 
       function(qtl) cindex( list(matrix( -lpnew, nrow = nrow(TE))), 
        formula = Surv(time, status) ~ x,
        data = TE, 
        eval.times = quantile(TR$time, qtl))$AppC$matrix)
# [1] 0.5041490 0.5186850 0.5106746

Four elements are needed for computing truncated C-statistic using survAUC::UnoC. But it seems pec::cindex does not need the training data.
- training data including covariates,
- testing data including covariates,
- predictor from new data,
- truncation time/evaluation time/prediction horizon.
(From ?UnoC) Uno's estimator is based on inverse-probability-of-censoring weights and does not assume a specific working model for deriving the predictor lpnew. It is assumed, however, that there is a one-to-one relationship between the predictor and the expected survival times conditional on the predictor. Note that the estimator implemented in UnoC is restricted to situations where the random censoring assumption holds.
survAUC::UnoC(). The tau parameter: Truncation time. The resulting C tells how well the given prediction model works in predicting events that occur in the time range from 0 to tau. [math]\displaystyle{ P(\beta'Z_1 \gt \beta' Z_2|T_1 \lt T_2, T_1 \lt \tau). }[/math] Con: no confidence interval estimate for [math]\displaystyle{ C_\tau }[/math] nor [math]\displaystyle{ C_\tau^{(A)} - C_\tau^{(B)} }[/math]
pec::cindex(). At each timepoint of eval.times the c-index is computed using only those pairs where one of the event times is known to be earlier than this timepoint. If eval.times is missing or Inf then the largest uncensored event time is used. See a more general example from here

Est.Cval() from the survC1 package (the only package gives confidence intervals of C-statistic or deltaC, authored by H. Uno). It doesn't take new data nor the vector of predictors obtained from the test data. Pro: Inf.Cval() can compute the confidence interval (perturbation-resampling based) of [math]\displaystyle{ C_\tau }[/math] & Inf.Cval.Delta() for the difference [math]\displaystyle{ C_\tau^{(A)} - C_\tau^{(B)} }[/math].

library(survAUC)
# require training and predict sets
TR <- ovarian[1:16,]
TE <- ovarian[17:26,]
train.fit  <- coxph(Surv(futime, fustat) ~ age, data=TR)

lpnew <- predict(train.fit, newdata=TE)
Surv.rsp <- Surv(TR$futime, TR$fustat)
Surv.rsp.new <- Surv(TE$futime, TE$fustat)              

UnoC(Surv.rsp, Surv.rsp, train.fit$linear.predictors, time=365.25*1) 
# [1] 0.9761905
UnoC(Surv.rsp, Surv.rsp, train.fit$linear.predictors, time=365.25*2) 
# [1] 0.7308979
UnoC(Surv.rsp, Surv.rsp, train.fit$linear.predictors, time=365.25*3) 
# [1] 0.7308979
UnoC(Surv.rsp, Surv.rsp, train.fit$linear.predictors, time=365.25*4) 
# [1] 0.7308979
UnoC(Surv.rsp, Surv.rsp, train.fit$linear.predictors, time=365.25*5) 
# [1] 0.7308979
UnoC(Surv.rsp, Surv.rsp, train.fit$linear.predictors)
# [1] 0.7308979
# So the function UnoC() can obtain the exact result as Est.Cval().
# Now try on a new data set. Question: why do we need Surv.rsp?
UnoC(Surv.rsp, Surv.rsp.new, lpnew)
# [1] 0.7333333
UnoC(Surv.rsp, Surv.rsp.new, lpnew, time=365.25*2)
# [1] 0.7333333

library(pec)
cindex( list(matrix( -lpnew, nrow = nrow(TE))), 
        formula = Surv(futime, fustat) ~ age,
        data = TE, eval.times = 365.25*2)$AppC
# $matrix
# [1] 0.7333333

library(survC1)
Est.Cval(cbind(TE, lpnew), tau = 365.25*2, nofit = TRUE)$Dhat
# [1] 0.7333333

# tau is mandatory (>0), no need to have training and predict sets
Est.Cval(ovarian[1:16, c(1,2, 3)], tau=365.25*1)$Dhat
# [1] 0.9761905
Est.Cval(ovarian[1:16, c(1,2, 3)], tau=365.25*2)$Dhat
# [1] 0.7308979
Est.Cval(ovarian[1:16, c(1,2, 3)], tau=365.25*3)$Dhat
# [1] 0.7308979
Est.Cval(ovarian[1:16, c(1,2, 3)], tau=365.25*4)$Dhat
# [1] 0.7308979
Est.Cval(ovarian[1:16, c(1,2, 3)], tau=365.25*5)$Dhat
# [1] 0.7308979

svg("~/Downloads/c_stat_scatter.svg", width=8, height=5)
par(mfrow=c(1,2))
plot(TR$futime, train.fit$linear.predictors, main="training data", 
     xlab="time", ylab="predictor")
mtext("C=.731 at t=2", 3)
plot(TE$futime, lpnew, main="testing data", xlab="time", ylab="predictor")
mtext("C=.733 at t=2", 3)
dev.off()

File:C stat scatter.svg

Assessing the prediction accuracy of a cure model for censored survival data with long-term survivors: Application to breast cancer data
The use of ROC for defining the validity of the prognostic index in censored data
Use and Misuse of the Receiver Operating Characteristic Curve in Risk Prediction Cook 2007
Evaluating Discrimination of Risk Prediction Models: The C Statistic by Pencina et al, JAMA 2015
Blanche et al(2018) The c-index is not proper for the evaluation of t-year predicted risks
- There is a bug on script line 154.
- With a fixed prediction horizon, the concordance index can be higher for a misspecified model than for a correctly specified model. The time-dependent AUC does not have this problem.
- (page 8) We now show that when a misspecified prediction model satisfies the ranking condition but the true distribution does not, then it is possible that the misspecified model achieves a misleadingly high c-index.
- The traditional C‐statistic used for the survival models is not guaranteed to identify the “best” model for estimating the risk of t-year survival. In contrast, measures of predicted error do not suffer from these limitations. See this paper The relationship between the C‐statistic and the accuracy of program‐specific evaluations by Wey et al 2018
- Unfortunately, a drawback of Harrell’s c-index for the time to event and competing risk settings is that the measure does not provide a value specific to the time horizon of prediction (e.g., a 3-year risk). See this paper The index of prediction accuracy: an intuitive measure useful for evaluating risk prediction models by Kattan and Gerds 2018.
- In Fig 1 Y-axis is concordance (AUC/C) and X-axis is time, the caption said The ability of (some variable) to discriminate patients who will either die or be transplanted within the next t-years from those who will be event-free at time t.
- The [math]\displaystyle{ \tau }[/math] considered here is the maximal end of follow-up time
- AUC (riskRegression::Score()), Uno-C (pec::cindex()), Harrell's C (Hmisc::rcorr.cens() for censored and summary(fit)$concordance for uncensored) are considered.
- The C_IPCW(t) or C_Harrell(t) is obtained by artificially censoring the outcome at time t. So C_IPCW(t) is different from Uno's version.

C-statistic limitations

See the discussion section of The relationship between the C‐statistic and the accuracy of program‐specific evaluations by Wey 2018

Correctly specified models can have low or high C‐statistics. Thus, the C‐statistic cannot identify a correctly specified model.
the traditional C‐statistic used for the survival models is not guaranteed to identify the “best” model for estimating the risk of, for example, 1‐year survival

Importantly, there exists no measure of risk discrimination or predicted error that can identify a correctly specified model, because they all depend on unknown characteristics of the data. For example, the C‐statistic depends on the variability in recipient‐level risk, while measures of squared error such as the Brier Score depend on residual variability.

Analysis of Biomarker Data: logs, odds ratios and ROC curves. This paper does not consider the survival time data. It has some summary about C-statistic (interpretation, warnings).

The C-statistic is relatively insensitive to the added contribution of a new marker when the two models, with and without biomarker, estimate risk on a continuous scale. In fact, many new biomarkers provide only minimal increase in the C-statistic when added to the Framingham model for CHD risk.
The classical C-statistic assumes that high sensitivity and high specificity are equally desirable. This is not always the case – for example, when screening the general population for a low-prevalence outcome requiring invasive follow-up, high specificity is important, while cancer screening in a high-risk group would emphasize high sensitivity.
To achieve a noticeable increase in the C-statistic, a biomarker must have a very strong independent association with the event risk (say ORs of 10 or higher per 1 SD increase).

C-statistic applications

Semiparametric Regression Analysis of Multiple Right- and Interval-Censored Events by Gao et al, JASA 2018
A c statistic of 0.7–0.8 is considered good, while >0.8 is considered excellent. See this paper. 2018
The C statistic, also termed concordance statistic or c-index, is analogous to the area under the curve and is a global measure of model discrimination. Discrimination refers to the ability of a risk prediction model to separate patients who develop a health outcome from patients who do not develop a health outcome. Effectively, the C statistic is the probability that a model will result in a higher-risk score for a patient who develops the outcomes of interest compared with a patient who does not develop the outcomes of interest. See the paper JAMA 2018

C-statistic vs LRT comparing nested models

1. Binary data

# https://stats.stackexchange.com/questions/46523/how-to-simulate-artificial-data-for-logistic-regression
set.seed(666)
x1 = rnorm(1000)           # some continuous variables 
x2 = rnorm(1000)
z = 1 + 2*x1 + 3*x2        # linear combination with a bias
pr = 1/(1+exp(-z))         # pass through an inv-logit function
y = rbinom(1000,1,pr)      # bernoulli response variable
df = data.frame(y=y,x1=x1,x2=x2)
fit <- glm( y~x1+x2,data=df,family="binomial")
summary(fit) 
# Estimate Std. Error z value Pr(>|z|)    
# (Intercept)   0.9915     0.1185   8.367   <2e-16 ***
#   x1            2.2731     0.1789  12.709   <2e-16 ***
#   x2            3.1853     0.2157  14.768   <2e-16 ***
#   ---
#   Signif. codes:  0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1
# 
# (Dispersion parameter for binomial family taken to be 1)
# 
# Null deviance: 1355.16  on 999  degrees of freedom
# Residual deviance:  582.93  on 997  degrees of freedom
# AIC: 588.93
confint.default(fit)
#                 2.5 %   97.5 %
# (Intercept) 0.7592637 1.223790
# x1          1.9225261 2.623659
# x2          2.7625861 3.608069

# LRT - likelihood ratio test
fit2 <- glm( y~x1,data=df,family="binomial")
anova.res <- anova(fit2, fit)
# Analysis of Deviance Table
# 
# Model 1: y ~ x1
# Model 2: y ~ x1 + x2
#   Resid. Df Resid. Dev Df Deviance
# 1       998    1186.16            
# 2       997     582.93  1   603.23
1-pchisq( abs(anova.res$Deviance[2]), abs(anova.res$Df[2]))
# [1] 0

# Method 1: use ROC package to compute AUC
library(ROC)
set.seed(123)
markers <- predict(fit, newdata = data.frame(x1, x2), type = "response")
roc1 <- rocdemo.sca( truth=y, data=markers, rule=dxrule.sca )
auc <- AUC(roc1); print(auc) # [1] 0.9459085

markers2 <- predict(fit2, newdata = data.frame(x1), type = "response")
roc2 <- rocdemo.sca( truth=y, data=markers2, rule=dxrule.sca )
auc2 <- AUC(roc2); print(auc2) # [1] 0.7259098
auc - auc2 # [1] 0.2199987

# Method 2: use pROC package to compute AUC
roc_obj <- pROC::roc(y, markers)
pROC::auc(roc_obj) # Area under the curve: 0.9459

# Method 3: Compute AUC by hand
# https://www.r-bloggers.com/calculating-auc-the-area-under-a-roc-curve/
auc_probability <- function(labels, scores, N=1e7){
  pos <- sample(scores[labels], N, replace=TRUE)
  neg <- sample(scores[!labels], N, replace=TRUE)
  # sum( (1 + sign(pos - neg))/2)/N # does the same thing
  (sum(pos > neg) + sum(pos == neg)/2) / N # give partial credit for ties
}
auc_probability(as.logical(y), markers) # [1] 0.945964

2. Survival data

library(survival)
data(ovarian)
head(ovarian)
range(ovarian$futime) # [1]   59 1227
plot(survfit(Surv(futime, fustat) ~ 1, data = ovarian))

coxph(Surv(futime, fustat) ~ rx + age, data = ovarian)
#        coef exp(coef) se(coef)     z      p
# rx  -0.8040    0.4475   0.6320 -1.27 0.2034
# age  0.1473    1.1587   0.0461  3.19 0.0014
#
# Likelihood ratio test=15.9  on 2 df, p=0.000355
# n= 26, number of events= 12 

require(survC1)
covs0 <- as.matrix(ovarian[, c("rx")])
covs1 <- as.matrix(ovarian[, c("rx", "age")])
tau=365.25*1
Delta=Inf.Cval.Delta(ovarian[, 1:2], covs0, covs1, tau, itr=200)
round(Delta, digits=3)
#          Est    SE Lower95 Upper95
# Model1 0.844 0.119   0.611   1.077
# Model0 0.659 0.148   0.369   0.949
# Delta  0.185 0.197  -0.201   0.572

Comparing differences in AUC from 2 different models

Time dependent ROC curves

tdrocc()

Calibration

Graphical calibration curves and the integrated calibration index (ICI) for survival models

Prognostic markers vs predictive markers (and other biomarkers)

Types of gene signature
Prognostic marker (某種疾病的危險因子) are biomarkers used to measure the progress of a disease in the patient sample. Prognostic markers are useful to stratify the patients into groups, guiding towards precise medicine discovery. Prognostic markers inform about likely disease outcome independent of the treatment received. See Statistical and practical considerations for clinical evaluation of predictive biomarkers by Mei-Yin Polley et al 2013.
Predictive marker/treatment selection markers provide information about likely outcomes with application of specific interventions. See Measuring the performance of markers for guiding treatment decisions by Janes, et al 2011.
The Fundamental Difficulty With Evaluating the Accuracy of Biomarkers for Guiding Treatment Janes 2015 , jnci
Designing a study to evaluate the benefit of a biomarker for selecting patient treatment Janes 2015
Statistical controversies in clinical research: prognostic gene signatures are not (yet) useful in clinical practice by Michiels 2016.
Prognostic (the likely course of the disease) ability = the capacity to predict the likely progression or outcome of a disease.
Diagnostic biomarker, prognostic biomarker and predictive biomarkers. Disease-related biomarkers and drug-related biomarkers. https://en.wikipedia.org/wiki/Biomarker_(medicine)
Diagnostic biomarker, prognostic biomarker and predictive biomarkers. https://en.wikipedia.org/wiki/Cancer_biomarker
Diagnostic (確定是某種疾病): diagnose conditions, as in the case of identifying early stage cancers
Statistical methods for building better biomarkers of chronic kidney disease by Pencina et al 2019.
Qualitative and quantitative interactions from Interaction (statistics)
- A plot of Interactions from STAT 509 Design and Analysis of Clinical Trials.
Understanding Prognostic versus Predictive Biomarkers 2016. No author. Not a good example to use. x-axis is time? File:Progpreg.png
- Example of a biomarker that is prognostic but not predictive (fig1)
- A biomarker that is both prognostic (negatively) and predictive (fig2)
- quantitative treatment-by-biomarker statistical interaction (fig3). Treatment effect 方向不變但是程度不同 in two subsets.
- qualitative treatment-by-biomarker interaction (fig4). There is a change in direction of treatment effects in two subsets (biomarker-positive/biomarker-negative). In particular, if the treatment has downsides such as toxicity or cost, it is compelling to consider treating only subjects with sufficiently large treatment effects (Vickers et al., 2007; Janes et al., 2013).
From the paper "Case-Only Approach to Identifying Markers Predicting Treatment Effects on the Relative Risk Scale" by Dai, Biometrics 2018
- For most clinical applications, a qualitative marker-by- treatment interaction is desired: the marker is useful if it identifies subgroups with treatment effects opposite in sign from the overall treatment effect.
- However, there are clinical applications where a quantitative– but not qualitative– marker-by-treatment interaction may be sufficient for a marker to be useful for treatment selection.
- A limitation of the case-only approach is its requirement that the endpoint of RCT has to be binary,
Biomarker: Predictive or Prognostic? by Karla V. Ballman, 2015. Lots of cites. File:Zlj9991056240002.jpeg
- A prognostic biomarker informs about a likely cancer outcome independent of treatment received. For a pure prognostic biomarker, the difference between Treat and STD in biomarker-A group is similar to the difference between Treat and STD in biomarker-B group. In other words, if a biomarker is prognostic and treatment is efficacious, the treatment benefit is similar for biomarker-positive and biomarker-negative patients. 比較 HR from 2 groups 就可確定是否 biomarker is prognostic 或是 test beta(biomarker) = 0 from fitting a Cox model with Treat + biomarker + Treat:biomarker. See Fig 1A or Fig 2A for a (pure) prognostic biomarker. Common examples include PSA level for prostate cancer and PIK3CA mutation status of tumors in women with HER2-positive metastatic breast cancer.
- A biomarker is predictive if the treatment effect is different for biomarker-positive patients compared with biomarker-negative patients. (However, the paper never defines what is biomarker-positive; it could be samples with some biomarker >0 or over-expressed). Test beta(biomarker*Treat) =0 from fitting a Cox model with Treat + biomarker + Treat:biomaker 就可以知道是否 predictive biomarker.
  - A qualitative interaction = pure predictive occurs when one biomarker group obtains benefit from treatment and the other group obtains no benefit (or is harmed) from treatment. The definition also appeared at Testing for qualitative interactions between treatment effects and patient subsets. 計算 HR from two groups. 如果一組 HR=1 (or >1) 另一組 HR <1, 就是 qualitative interaction. See Fig 1C or Fig 2B.
  - Both groups derived benefit from the treatment, this is a quantitative interaction = both prognostic & predictive. See Fig 1B or Fig 2C.
- Fig2 A. A purely prognostic biomarker. X-axis is time. Left is biomarker-negative patients and RHS is biomarker-positive patients. Biomarker-positive patients have a better survival than Biomarker-negative patients independent of treatment group.
- Fig2 B. A purely predictive marker.
- Fig2 C. A biomarker is both predictive and prognostic. This is also an example of a quantitative interaction.
Prognostic vs. Predictive Biomarkers from Clinical OMICs.
The area between ROC curves, a non-parametric method to evaluate a biomarker for patient treatment selection Blangero 2020. quantitative markers
Distinguishing prognostic and predictive biomarkers: an information theoretic approach Sechidis 2018, Bioinformatics.
- This uses a more mathematical way to discuss several issues.
Prognostic factors versus predictive factors: Examples from a clinical trial of erlotinib Clark 2008.
Construction and optimization of gene expression signatures for prediction of survival in two-arm clinical trials by Joachim Theilhaber et al 2020
Evidence for Treatment-by-Biomarker interaction for FDA-approved Oncology Drugs with Required Pharmacogenomic Biomarker Testing 2017
Evaluation of biomarkers for treatment selection using individual participant data from multiple clinical trials Kang 2018. Simulations.
Distinguishing prognostic and predictive biomarkers: an information theoretic approach Sechidis 2018
On evaluating how well a biomarker can predict treatment response with survival data Mboup 2020
Estimation of Optimal Individualized Treatment Rules Using a Covariate-Specific Treatment Effect Curve With High-Dimensional Covariates Guo 2021, jasa
Robust method for optimal treatment decision making based on survival data Fang 2021

Prognostic biomarkers

Detecting prognostic biomarkers of breast cancer by regularized Cox proportional hazards models Li 2021. prognostic risk score (PRS), training, discovery dataset, independent, validation, enrichment analysis, C-index, overlap, GEO

biospear package

Applications based on google scholar on biospear package paper:

Gene Expression Signature Correlates with Outcomes in Metastatic Renal Cell Carcinoma Patients Treated with Everolimus Alone or with a Vascular Disrupting Agent 2021
Transcription factor networks of oligodendrogliomas treated with adjuvant radiotherapy or observation inform prognosis 2020. “biospear” package to generate a prognostic signature. We describe efforts to integrate clinical genomics to discover predictive bio-markers that would inform adjuvant treatment decisions in oligodendrogliomas ... A second prognostic signature for patients treated with observation alone was also developed, representing a predictive bio-marker for patients who would benefit from adjuvant radiotherapy.

Treatment Effect

Tian 2014: [math]\displaystyle{ P(T^1 \geq t_0|z) - P(T^{-1} \geq t_0|z) }[/math]
Bonetti 2000: Hazard ratio
Janes 2014: [math]\displaystyle{ \Delta(Y) = \rho_0(Y) - \rho_1(Y) = P(D=1|T=0, Y) - P(D=1|T=1, Y) }[/math]
- Subjects with [math]\displaystyle{ \Delta(Y)\lt 0 }[/math] are called marker-negative; standard/controlled treatment is favored.
- Subjects with [math]\displaystyle{ \Delta(Y)\gt 0 }[/math] are called marker-positive; new treatment is favored. The rule is applying treatment onlyto marker-positive patients. And for this portion of patients, the average benefit of treatment is calculated by [math]\displaystyle{ B_{pos} = E(\Delta(Y) | \Delta(Y) \gt 0) }[/math]. See p103 on the paper.

Subgroup identification

STEPP/subpopulation treatment effect pattern plot: Evaluation of treatment-effect heterogeneity using biomarkers measured on a continuous scale Lazar 2010 (NIH pubmed). CRAN R package.
- Some random articles citing the above paper
- Some disadvantages are discussed in Investigating treatment-effect modification by a continuous covariate in IPD meta-analysis: an approach using fractional polynomials 2022
- Prognostic values of clinical and molecular features in HER2 low-breast cancer with hormonal receptor overexpression: features of HER2-low breast cancer 2022
- The platelet to lymphocyte ratio is a potential inflammatory marker predicting the effects of adjuvant chemotherapy in patients with stage II colorectal cancer 2021
Tutorial in biostatistics: data-driven subgroup identification and analysis in clinical trials Lipkovich 2016
Identification of subgroups via partial linear regression modeling approach Zhou 2021

Some packages

personalized package

personalized: Estimation and Validation Methods for Subgroup Identification and Personalized Medicine. Subgroup Identification and Precision Medicine with the {personalized} R Package (youtube)

SurvMetrics

SurvMetrics: Predictive Evaluation Metrics in Survival Analysis

SurvBenchmark

SurvBenchmark: comprehensive benchmarking study of survival analysis methods using both omics data and clinical data

Lasso estimation of hierarchical interactions for analyzing heterogeneity of treatment effect

Lasso estimation of hierarchical interactions for analyzing heterogeneity of treatment effect 2021

Quantifying treatment differences in confirmatory trials under non-proportional hazards

The source code in Github.

Computation for gene expression (microarray) data

survival package (basic package, not designed for gene expression)
gsa package
samr package
pamr package
(Bioconductor) genefilter, source. genefilter() & coxfilter(). apply() was used.
logpl() from survcomp package

n <- 500
g <- 10000
y <- rexp(n)
status <- ifelse(runif(n) < .7, 1, 0)
x <- matrix(rnorm(n*g), nr=g)
treat <- rbinom(n, 1, .5)
# Method 1
system.time(for(i in 1:g) coxph(Surv(y, status) ~ x[i, ] + treat + treat:x[i, ]))
# 28 seconds 

# Method 2
system.time(apply(x, 1, function(z) coxph(Surv(y, status) ~ z + treat + treat:z)))
# 29 seconds

# Method 3 (Windows)
dyn.load("C:/Program Files (x86)/ArrayTools/Fortran/surv64.dll")			  
tme <- y
sorted <- order(tme)
stime <- as.double(tme[sorted])
sstat <- as.integer(status[sorted])
x1 <- x[,sorted]
imodel <- 1  # imodel=1, fit univariate gene expression. Return p-values vector.
nvar <- 1
system.time(outx1 <- .Fortran("coxfitc", as.integer(n), as.integer(g), as.integer(0),
                 stime, sstat, t(x1), as.double(0), as.integer(imodel), 
                 double(2*n+2*nvar*nvar+3*nvar), logdiff = double(g)))
# 1.69 seconds on R i386
# 0.79 seconds on R x64

# method 4: GSA
genenames=paste("g", 1:g, sep="")
#create some random gene sets
genesets=vector("list", 50)
for(i in 1:50){
  genesetsi=paste("g", sample(1:g,size=30), sep="")
}
geneset.names=paste("set",as.character(1:50),sep="")
debug(GSA.func)
GSA.obj<-GSA(x,y, genenames=genenames, genesets=genesets,  
             censoring.status=status,
             resp.type="Survival", nperms=1)
Browse[3]> str(catalog.unique)
 int [1:1401] 7943 227 4069 3011 8402 1586 2443 2777 673 9021 ...
Browse[3]> system.time(cox.func(x[catalog.unique,], y, censoring.status, s0=0))
# 1.3 seconds
Browse[2]> system.time(cox.func(x, y, censoring.status, s0=0))
# 7.259 seconds

Single gene vs mult-gene survival models

A comparative study of survival models for breast cancer prognostication revisited: the benefits of multi-gene models by Grzadkowski et al 2018. To concordance of biomarker performance, the authors use the Concordance Correlation Coefficient (CCC) as introduced by Lin (1989) and further amended in Lin (2000).

Random papers using C-index, AUC or Brier scores

Predicting the Survival Time for Bladder Cancer Using an Additive Hazards Model in Microarray Data 2016. AUC, Brier scores and C-index were used

survex package

survex: model-agnostic explainability for survival analysis

More, Web tools

This pdf file from data.princeton.edu contains estimation, hypothesis testing, time varying covariates and baseline survival estimation.
Survival analysis: basic terms, the exponential model, censoring, examples in R and JAGS
Survival analysis is not commonly used to predict future times to an event. Cox model would require specification of the baseline hazard function.
SurvExpress: An Online Biomarker Validation Tool and Database for Cancer Gene Expression Data Using Survival Analysis 2013. JSP, Javascript, MySQL, Ajax, R & Apache. Public datasets were obtained from GEO, TCGA, ArrayExpress.

Others

Landmark analysis

A landmark analysis for survival data is a statistical method used in survival analysis. It involves designating a specific time point during the follow-up period, known as the landmark time, and analyzing only those subjects who have survived until the landmark time. Landmark analysis: A primer.
- This method is often used to estimate survival probabilities in an unbiased way, conditional on the group membership of patients at the landmark time. A small number of index time points are chosen and survival analysis is done on only those subjects who remain event-free at the specified index times and for follow-up beyond the index times. Landmark Analysis at the 25-Year Landmark Point 2011 & A comparison of landmark methods and time-dependent ROC methods to evaluate the time-varying performance of prognostic markers for survival outcomes 2019.
- Landmark analysis can help avoid certain types of bias, such as the guarantee-time bias or the immortal time bias. It's particularly useful when patient predictions are needed at select times, and it facilitates evaluating trends in performance over time.
- In the context of survival data, which consist of a distinct start time and end time, landmark analysis provides a valuable tool for understanding and predicting future disease events. It's often used in clinical practice to guide medical decision-making.

TCGA data

Survival Analysis of Breast Cancer Data from the TCGA Dataset
Survival Analysis with R
SmulTCan: A Shiny application for multivariable survival analysis of TCGA data with gene sets, 2021
GNOSIS: an R Shiny app supporting cancer genomics survival analysis with cBioPortal, 2022

Machine learning

mlr3proba: an R package for machine learning in survival analysis
survivalmodels Currently implemented are five neural networks from the Python packages pycox, DNNSurv, and the Akritas non-parametric conditional estimator. Further updates will include implementations of novel survival models.
SurvivalML: an integrative platform for the discovery and exploration of prognostic models in multi-center cancer cohorts 2022

Constrained randomization

Constrained randomization to evaulate the vaccine rollout in nursing homes

Principles and Practice of Clinical Research

Clinical trials

Statistical Thinking in Clinical Trials

Fundamental Statistical Concepts in Clinical Trials and Diagnostic Testing

JNM 2021

Statistical Monitoring of Clinical Trials: A Unified Approach

ebook on archive.org.

Principles of Clinical Pharmacology

Progressive disease, stable disease

RECIST/Response evaluation criteria in solid tumors:
- CR Complete response: This is the best response. It means that all signs of the cancer have disappeared in the tests. There’s no evidence of disease present.
- PR Partial response: This means the cancer has significantly reduced in size but is still detectable.
- SD Stable disease: This means the cancer has neither grown nor shrunk. The disease is stable. SD may or may not be considered as a responder. In some cases, maintaining stable disease might be seen as a good response, especially for cancers that are typically very aggressive or hard to treat.
- PD Progressive disease: This is the worst response. It means the cancer has grown or spread to other parts of the body.
Stable Disease in Cancer Treatment. Stable disease is defined as being a little better than progressive disease (in which a tumor has increased in size by at least 20%) and a little worse than a partial response (wherein a tumor has shrunk by at least 50%).
Ideally a drug trial will return results like CR or PR. Responses of SD or PD may indicate that a drug is not an effective treatment for cancer. https://callaix.com/recist

STANDARD OF CARE

Everyone would receive (which may be no therapy) if no biomarker was used. Cf: experimental therapy with effect that might be relatedto the value of a continuous biomarker.

Breast cancer

HER2-positive breast cancer

Tumor markers of breast cancer: New prospectives Kabel 2017
https://www.mayoclinic.org/breast-cancer/expert-answers/FAQ-20058066
https://en.wikipedia.org/wiki/Trastuzumab (antibody, injection into a vein or under the skin)
A Three-Gene Model to Robustly Identify Breast Cancer Molecular Subtypes, genefu package, package paper. Breast cancer is categorized into at least four clinically relevant molecular subtypes that reflect upon expression levels of specific genes
- Her2-enriched (also called HER2+),
- ‘Triple-negative breast cancers” (ER−/HER2−/PR−, similar to basal-like) and
- ‘Luminal-like’ which are mainly ER+/HER2− that could be further discriminated into luminal A and B based on their low and high proliferative phenotype, respectively.
ER+, HER2+ means samples. ESR1, ERBB2 means gene. See the genefu vignettte. It seems the gene AURKA has a higher concordance index compared to ESR1, ERBB2 and PIK3CA. The article also mentioned about clustering based method.
Prognostic and predictive biomarkers in breast cancer: Past, present and future Nicolini 2018
Prognostic and predictive markers for breast cancer management
ESR1 mutations found prognostic but not predictive in metastatic breast cancer
Prognostic and predictive role of ESR1 status for postmenopausal patients with endocrine-responsive early breast cancer in the Danish cohort of the BIG 1-98 trial
Estrogen receptor 1 and progesterone receptor are distinct biomarkers and prognostic factors in estrogen receptor-positive breast cancer: Evidence from a bioinformatic analysis
- ESR1 and PGR are highly expressed in ER-positive breast cancers than in ER-negative BC.
- In ER+ patients, the expression levels of ESR1 and PGR genes are associated with relapse-free survival (RFS). HR_ESR1>1 & HR_PGR<1.
Single cell research identifies how the most common type of breast cancer becomes resistant to treatment 2021
In HER-2 positive breast cancers, tumor cells carry a particular protein (HER2) that helps them grow. Certain drugs, like Herceptin (trastuzumab), target that protein. See Researchers Find Better Way to Fight Breast Cancer That Has Spread to Brain
Five crucial prognostic-related autophagy genes stratified female breast cancer patients aged 40–60 years
乳癌的分期與類型

TNBC (Triple-negative breast cancer)

https://en.wikipedia.org/wiki/TNBC

Patient ID	Start Time	Stop Time	Status	Dosage
1	0	3	0	10
1	3	6	1	20
2	0	2	0	10
2	2	5	0	15
2	5	8	1	15

Survival data: Difference between revisions