comp.risk: Competings Risks Regression in timereg: Flexible Regression Models for Survival Data (2024)

comp.riskR Documentation

Competings Risks Regression

Description

Fits a semiparametric model for the cause-specific quantities :

for a known link-functionh() and known prediction-function g(t,x,z) for the probabilityof dying from cause 1 in a situation with competing causes of death.

Usage

comp.risk( formula, data = parent.frame(), cause, times = NULL, Nit = 50, clusters = NULL, est = NULL, fix.gamma = 0, gamma = 0, n.sim = 0, weighted = 0, model = "fg", detail = 0, interval = 0.01, resample.iid = 1, cens.model = "KM", cens.formula = NULL, time.pow = NULL, time.pow.test = NULL, silent = 1, conv = 1e-06, weights = NULL, max.clust = 1000, n.times = 50, first.time.p = 0.05, estimator = 1, trunc.p = NULL, cens.weights = NULL, admin.cens = NULL, conservative = 1, monotone = 0, step = NULL)

Arguments

formula

a formula object, with the response on the left of a '~'operator, and the terms on the right. The response must be a survival objectas returned by the ‘Event’ function. The status indicator is not importanthere. Time-invariant regressors are specified by the wrapper const(), andcluster variables (for computing robust variances) by the wrapper cluster().

data

a data.frame with the variables.

cause

For competing risk models specificies which cause we consider.

times

specifies the times at which the estimator is considered.Defaults to all the times where an event of interest occurs, with the first10 percent or max 20 jump points removed for numerical stability insimulations.

Nit

number of iterations for Newton-Raphson algorithm.

clusters

specifies cluster structure, for backwards compability.

est

possible starting value for nonparametric component of model.

fix.gamma

to keep gamma fixed, possibly at 0.

gamma

starting value for constant effects.

n.sim

number of simulations in resampling.

weighted

Not implemented. To compute a variance weighted version ofthe test-processes used for testing time-varying effects.

model

"additive", "prop"ortional, "rcif", or "logistic".

detail

if 0 no details are printed during iterations, if 1 detailsare given.

interval

specifies that we only consider timepoints where theKaplan-Meier of the censoring distribution is larger than this value.

resample.iid

to return the iid decomposition, that can be used toconstruct confidence bands for predictions

cens.model

specified which model to use for the ICPW, KM isKaplan-Meier alternatively it may be "cox"

cens.formula

specifies the regression terms used for the regressionmodel for chosen regression model. When cens.model is specified, the defaultis to use the same design as specified for the competing risks model.

time.pow

specifies that the power at which the time-arguments istransformed, for each of the arguments of the const() terms, default is 1for the additive model and 0 for the proportional model.

time.pow.test

specifies that the power the time-arguments istransformed for each of the arguments of the non-const() terms. This isrelevant for testing if a coefficient function is consistent with thespecified form A_l(t)=beta_l t^time.pow.test(l). Default is 1 for theadditive model and 0 for the proportional model.

silent

if 0 information on convergence problems due to non-invertiblederviates of scores are printed.

conv

gives convergence criterie in terms of sum of absolute change ofparameters of model

weights

weights for estimating equations.

max.clust

sets the total number of i.i.d. terms in i.i.d.decompostition. This can limit the amount of memory used by coarsening theclusters. When NULL then all clusters are used. Default is 1000 to savememory and time.

n.times

only uses 50 points for estimation, if NULL then uses allpoints, subject to p.start condition.

first.time.p

first point for estimation is pth percentile of causejump times.

estimator

default estimator is 1.

trunc.p

truncation weight for delayed entry, P(T > entry.time | Z_i),typically Cox model.

cens.weights

censoring weights can be given here rather thancalculated using the KM, cox or aalen models.

admin.cens

censoring times for the administrative censoring

conservative

set to 0 to compute correct variances based on censoringweights, default is conservative estimates that are much quicker.

monotone

monotone=0, uses estimating equations

montone=1 uses

step

step size for Fisher-Scoring algorithm.

Details

We consider the following models : 1) the additive model whereh(x)=1-\exp(-x) and

2) the proportional setting that includes the Fine & Gray (FG) "prop"model and some extensions where h(x)=1-\exp(-\exp(x)) and

The FG model is obtainedwhen x=1, but the baseline is parametrized as \exp(A(t)).

The "fg" model is a different parametrization that contains the FG model,where h(x)=1-\exp(-x) and

The FG model is obtained when x=1.

3) a "logistic" model where h(x)=\exp(x)/( 1+\exp(x)) and

The "logistic2" is

The simple logistic model withjust a baseline can also be fitted by an alternative procedure that hasbetter small sample properties see prop.odds.subist().

4) the relative cumulative incidence function "rcif" model whereh(x)=\exp(x) and

The "rcif2"

Where p by default is 1 for the additive model and 0 for the other models.In general p may be powers of the same length as z.

Since timereg version 1.8.4. the response must be specified with theEvent function instead of the Surv function andthe arguments. For example, if the old code was

comp.risk(Surv(time,cause>0)~x1+x2,data=mydata,cause=mydata$cause,causeS=1)

the new code is

comp.risk(Event(time,cause)~x1+x2,data=mydata,cause=1)

Also the argument cens.code is now obsolete since cens.code is an argumentof Event.

Value

returns an object of type 'comprisk'. With the following arguments:

cum

cumulative timevarying regression coefficient estimates arecomputed within the estimation interval.

var.cum

pointwise variancesestimates.

gamma

estimate of proportional odds parameters ofmodel.

var.gamma

variance for gamma.

score

sum of absolutevalue of scores.

gamma2

estimate of constant effects based on thenon-parametric estimate. Used for testing of constant effects.

obs.testBeq0

observed absolute value of supremum of cumulativecomponents scaled with the variance.

pval.testBeq0

p-value forcovariate effects based on supremum test.

obs.testBeqC

observedabsolute value of supremum of difference between observed cumulative processand estimate under null of constant effect.

pval.testBeqC

p-valuebased on resampling.

obs.testBeqC.is

observed integrated squareddifferences between observed cumulative and estimate under null of constanteffect.

pval.testBeqC.is

p-value based on resampling.

conf.band

resampling based constant to construct 95% uniformconfidence bands.

B.iid

list of iid decomposition of non-parametriceffects.

gamma.iid

matrix of iid decomposition of parametriceffects.

test.procBeqC

observed test process for testing oftime-varying effects

sim.test.procBeqC

50 resample processes for fortesting of time-varying effects

conv

information on convergence fortime points used for estimation.

Author(s)

Thomas Scheike

References

Scheike, Zhang and Gerds (2008), Predicting cumulative incidenceprobability by direct binomial regression,Biometrika, 95, 205-220.

Scheike and Zhang (2007), Flexible competing risks regression modelling andgoodness of fit, LIDA, 14, 464-483.

Martinussen and Scheike (2006), Dynamic regression models for survival data,Springer.

Examples

data(bmt); clust <- rep(1:204,each=2)addclust<-comp.risk(Event(time,cause)~platelet+age+tcell+cluster(clust),data=bmt,cause=1,resample.iid=1,n.sim=100,model="additive")###addclust<-comp.risk(Event(time,cause)~+1+cluster(clust),data=bmt,cause=1, resample.iid=1,n.sim=100,model="additive")pad <- predict(addclust,X=1)plot(pad)add<-comp.risk(Event(time,cause)~platelet+age+tcell,data=bmt,cause=1,resample.iid=1,n.sim=100,model="additive")summary(add)par(mfrow=c(2,4))plot(add); ### plot(add,score=1) ### to plot score functions for testndata<-data.frame(platelet=c(1,0,0),age=c(0,1,0),tcell=c(0,0,1))par(mfrow=c(2,3))out<-predict(add,ndata,uniform=1,n.sim=100)par(mfrow=c(2,2))plot(out,multiple=0,uniform=1,col=1:3,lty=1,se=1)## fits additive model with some constant effects add.sem<-comp.risk(Event(time,cause)~const(platelet)+const(age)+const(tcell),data=bmt,cause=1,resample.iid=1,n.sim=100,model="additive")summary(add.sem)out<-predict(add.sem,ndata,uniform=1,n.sim=100)par(mfrow=c(2,2))plot(out,multiple=0,uniform=1,col=1:3,lty=1,se=0)## Fine & Gray model fg<-comp.risk(Event(time,cause)~const(platelet)+const(age)+const(tcell),data=bmt,cause=1,resample.iid=1,model="fg",n.sim=100)summary(fg)out<-predict(fg,ndata,uniform=1,n.sim=100)par(mfrow=c(2,2))plot(out,multiple=1,uniform=0,col=1:3,lty=1,se=0)## extended model with time-varying effectsfg.npar<-comp.risk(Event(time,cause)~platelet+age+const(tcell),data=bmt,cause=1,resample.iid=1,model="prop",n.sim=100)summary(fg.npar); out<-predict(fg.npar,ndata,uniform=1,n.sim=100)head(out$P1[,1:5]); head(out$se.P1[,1:5])par(mfrow=c(2,2))plot(out,multiple=1,uniform=0,col=1:3,lty=1,se=0)## Fine & Gray model with alternative parametrization for baselinefg2<-comp.risk(Event(time,cause)~const(platelet)+const(age)+const(tcell),data=bmt,cause=1,resample.iid=1,model="prop",n.sim=100)summary(fg2)################################################################### Delayed entry models, #################################################################nn <- nrow(bmt)entrytime <- rbinom(nn,1,0.5)*(bmt$time*runif(nn))bmt$entrytime <- entrytimetimes <- seq(5,70,by=1)bmtw <- prep.comp.risk(bmt,times=times,time="time",entrytime="entrytime",cause="cause")## non-parametric model outnp <- comp.risk(Event(time,cause)~tcell+platelet+const(age), data=bmtw,cause=1,fix.gamma=1,gamma=0, cens.weights=bmtw$cw,weights=bmtw$weights,times=times,n.sim=0)par(mfrow=c(2,2))plot(outnp)outnp <- comp.risk(Event(time,cause)~tcell+platelet, data=bmtw,cause=1, cens.weights=bmtw$cw,weights=bmtw$weights,times=times,n.sim=0)par(mfrow=c(2,2))plot(outnp)## semiparametric model out <- comp.risk(Event(time,cause)~const(tcell)+const(platelet),data=bmtw,cause=1, cens.weights=bmtw$cw,weights=bmtw$weights,times=times,n.sim=0)summary(out)
comp.risk: Competings Risks Regression in timereg: Flexible Regression Models for Survival Data (2024)

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