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Tip revision: 161d0aff86ac21b6cbd2619aa9a8f8e6f1f18eab authored by Charles Dupont on 31 October 2007, 00:00:00 UTC
version 3.4-3
Tip revision: 161d0af
cpower.Rd
\name{cpower}
\alias{cpower}
\title{
Power of Cox/log-rank Two-Sample Test
}
\description{
Assumes exponential distributions for both treatment groups.
Uses the George-Desu method along with
formulas of Schoenfeld that allow estimation of the expected number of
events in the two groups.  
To allow for drop-ins (noncompliance to control therapy, crossover to
intervention) and noncompliance of the intervention, the method of
Lachin and Foulkes is used.
}
\usage{
cpower(tref, n, mc, r, accrual, tmin, noncomp.c=0, noncomp.i=0, 
       alpha=0.05, nc, ni, pr=TRUE)
}
\arguments{
\item{tref}{
time at which mortalities estimated
}
\item{n}{
total sample size (both groups combined).  If allocation is unequal
so that there are not \code{n/2} observations in each group, you may specify
the sample sizes in \code{nc} and \code{ni}.
}
\item{mc}{
tref-year mortality, control
}
\item{r}{
\% reduction in \code{mc} by intervention
}
\item{accrual}{
duration of accrual period
}
\item{tmin}{
minimum follow-up time
}
\item{noncomp.c}{
\% non-compliant in control group (drop-ins)
}
\item{noncomp.i}{
\% non-compliant in intervention group (non-adherers)
}
\item{alpha}{
type I error probability.  A 2-tailed test is assumed.
}
\item{nc}{
number of subjects in control group
}
\item{ni}{
number of subjects in intervention group.  \code{nc} and \code{ni} are specified
exclusive of \code{n}.
}
\item{pr}{
set to \code{FALSE} to suppress printing of details
}}
\value{
power
}
\section{Side Effects}{
prints
}
\details{
For handling noncompliance, uses a modification of formula (5.4) of
Lachin and Foulkes.  Their method is based on a test for the difference
in two hazard rates, whereas \code{cpower} is based on testing the difference
in two log hazards.  It is assumed here that the same correction factor
can be approximately applied to the log hazard ratio as Lachin and Foulkes applied to
the hazard difference.


Note that Schoenfeld approximates the variance
of the log hazard ratio by \code{4/m}, where \code{m} is the total number of events,
whereas the George-Desu method uses the slightly better \code{1/m1 + 1/m2}.
Power from this function will thus differ slightly from that obtained with
the SAS \code{samsizc} program.
}
\author{
Frank Harrell
\cr
Department of Biostatistics
\cr
Vanderbilt University
\cr
f.harrell@vanderbilt.edu
}
\references{
Peterson B, George SL: Controlled Clinical Trials 14:511--522; 1993.


Lachin JM, Foulkes MA: Biometrics 42:507--519; 1986.


Schoenfeld D: Biometrics 39:499--503; 1983.
}
\seealso{
\code{\link{spower}}, \code{\link{ciapower}}, \code{\link{bpower}}
}
\examples{
#In this example, 4 plots are drawn on one page, one plot for each
#combination of noncompliance percentage.  Within a plot, the
#5-year mortality \% in the control group is on the x-axis, and
#separate curves are drawn for several \% reductions in mortality
#with the intervention.  The accrual period is 1.5y, with all
#patients followed at least 5y and some 6.5y.


par(mfrow=c(2,2),oma=c(3,0,3,0))


morts <- seq(10,25,length=50)
red <- c(10,15,20,25)


for(noncomp in c(0,10,15,-1)) {
  if(noncomp>=0) nc.i <- nc.c <- noncomp else {nc.i <- 25; nc.c <- 15}
  z <- paste("Drop-in ",nc.c,"\%, Non-adherence ",nc.i,"\%",sep="")
  plot(0,0,xlim=range(morts),ylim=c(0,1),
           xlab="5-year Mortality in Control Patients (\%)",
           ylab="Power",type="n")
  title(z)
  cat(z,"\n")
  lty <- 0
  for(r in red) {
        lty <- lty+1
        power <- morts
        i <- 0
        for(m in morts) {
          i <- i+1
          power[i] <- cpower(5, 14000, m/100, r, 1.5, 5, nc.c, nc.i, pr=FALSE)
        }
        lines(morts, power, lty=lty)
  }
  if(noncomp==0)legend(18,.55,rev(paste(red,"\% reduction",sep="")),
           lty=4:1,bty="n")
}
mtitle("Power vs Non-Adherence for Main Comparison",
           ll="alpha=.05, 2-tailed, Total N=14000",cex.l=.8)
#
# Point sample size requirement vs. mortality reduction
# Root finder (uniroot()) assumes needed sample size is between
# 1000 and 40000
#
nc.i <- 25; nc.c <- 15; mort <- .18
red <- seq(10,25,by=.25)
samsiz <- red


i <- 0
for(r in red) {
  i <- i+1
  samsiz[i] <- uniroot(function(x) cpower(5, x, mort, r, 1.5, 5,
                                          nc.c, nc.i, pr=FALSE) - .8,
                       c(1000,40000))$root
}


samsiz <- samsiz/1000
par(mfrow=c(1,1))
plot(red, samsiz, xlab='\% Reduction in 5-Year Mortality',
	 ylab='Total Sample Size (Thousands)', type='n')
lines(red, samsiz, lwd=2)
title('Sample Size for Power=0.80\nDrop-in 15\%, Non-adherence 25\%')
title(sub='alpha=0.05, 2-tailed', adj=0)
}
\keyword{htest}
\keyword{survival}
\concept{power}
\concept{study design}
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