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\alias{cch}\name{cch}\title{Fits proportional hazards regression model to case-cohort data}\description{ Returns estimates and standard errors from relative riskregression fit to data from case-cohort studies. A choice is availableamong the Prentice, Self-Prentice and Lin-Ying methods for unstratifieddata. For stratified data the choice is between Borgan I, ageneralization of the Self-Prentice estimator for unstratifiedcase-cohort data, and Borgan II, a generalization of the Lin-Yingestimator.}\usage{cch(formula, data = sys.parent(), subcoh, id, stratum=NULL, cohort.size,method =c("Prentice","SelfPrentice","LinYing","I.Borgan","II.Borgan"),robust=FALSE)}\arguments{\item{formula}{A formula object that must have a \code{\link{Surv}} object as the response.The Surv object must be of type \code{"right"}, or of type \code{"counting"}.}\item{subcoh}{Vector of indicatorsfor subjects sampled as part of thesub-cohort. Code \code{1} or \code{TRUE} for members of thesub-cohort, \code{0} or \code{FALSE} for others. If \code{data} is adata frame then \code{subcoh} may be a one-sided formula.}\item{id}{Vector of unique identifiers, or formula specifying such a vector.}\item{stratum}{A vector of stratum indicators or a formula specifyingsuch a vector}\item{cohort.size}{Vector with size of each stratum original cohort from which subcohort was sampled}\item{data}{An optional data frame in which to interpret the variablesoccurring in the formula.}\item{method}{Three procedures are available. The default method is "Prentice", withoptions for "SelfPrentice" or "LinYing". }\item{robust}{For \code{"LinYing"} only, if \code{robust=TRUE}, use design-based standard errors even forphase I}}\value{An object of class "cch" incorporating a list of estimated regression coefficients and two estimates of theirasymptotic variance-covariance matrix.\item{coef}{regression coefficients.}\item{naive.var}{Self-Prentice model based variance-covariance matrix.}\item{var}{Lin-Ying empirical variance-covariance matrix.}}\details{Implements methods for case-cohort data analysis described by Therneau andLi (1999). The three methods differ in the choice of "risk sets" used tocompare the covariate values of the failure with those of others at risk atthe time of failure. "Prentice" uses the sub-cohort members "at risk" plusthe failure if that occurs outside the sub-cohort and is score unbiased."SelfPren" (Self-Prentice) uses just the sub-cohort members "at risk". Thesetwo have the same asymptotic variance-covariance matrix. "LinYing" (Lin-Ying)uses the all members of the sub-cohort and all failures outside the sub-cohortwho are "at risk". The methods also differ in the weights given to differentscore contributions.The \code{data} argument must not have missing values for any variablesin the model. There must not be any censored observations outside the subcohort.}\author{Norman Breslow, modified by Thomas Lumley}\references{Prentice, RL (1986). A case-cohort design for epidemiologic cohort studies anddisease prevention trials. Biometrika 73: 1--11.Self, S and Prentice, RL (1988). Asymptotic distribution theory and efficiencyresults for case-cohort studies. Annals of Statistics 16: 64--81.Lin, DY and Ying, Z (1993). Cox regression with incomplete covariate measurements.Journal of the American Statistical Association 88: 1341--1349.Barlow, WE (1994). Robust variance estimation for the case-cohort design. Biometrics50: 1064--1072Therneau, TM and Li, H (1999). Computing the Cox model for case-cohort designs.Lifetime Data Analysis 5: 99--112.Borgan, \eqn{\O}{O}, Langholz, B, Samuelsen, SO, Goldstein, L and Pogoda, J (2000)Exposure stratified case-cohort designs. Lifetime Data Analysis 6, 39-58.}\seealso{\code{twophase} and \code{svycoxph} in the "survey" package formore general two-phase designs. \url{http://faculty.washington.edu/tlumley/survey/}}\examples{## The complete Wilms Tumor Data## (Breslow and Chatterjee, Applied Statistics, 1999)## subcohort selected by simple random sampling.##subcoh <- nwtco$in.subcohortselccoh <- with(nwtco, rel==1|subcoh==1)ccoh.data <- nwtco[selccoh,]ccoh.data$subcohort <- subcoh[selccoh]## central-lab histologyccoh.data$histol <- factor(ccoh.data$histol,labels=c("FH","UH"))## tumour stageccoh.data$stage <- factor(ccoh.data$stage,labels=c("I","II","III","IV"))ccoh.data$age <- ccoh.data$age/12 # Age in years#### Standard case-cohort analysis: simple random subcohort##fit.ccP <- cch(Surv(edrel, rel) ~ stage + histol + age, data =ccoh.data,subcoh = ~subcohort, id=~seqno, cohort.size=4028)fit.ccPfit.ccSP <- cch(Surv(edrel, rel) ~ stage + histol + age, data =ccoh.data,subcoh = ~subcohort, id=~seqno, cohort.size=4028, method="SelfPren")summary(fit.ccSP)#### (post-)stratified on instit##stratsizes<-table(nwtco$instit)fit.BI<- cch(Surv(edrel, rel) ~ stage + histol + age, data =ccoh.data,subcoh = ~subcohort, id=~seqno, stratum=~instit, cohort.size=stratsizes,method="I.Borgan")summary(fit.BI)}\keyword{survival}