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Here the simulation study setting is defined.
id <- 1
onset <- 3
a0 <- 2
a1 <- 3
refDose <- 56
# True dose-DLT relationship
myTruth <- function(dose) {
StandLogDose <- log(dose / refDose)
plogis(a0 + a1 * StandLogDose)
}
# The conditional CDF of the PEM
if (onset == 30) {
onset <- 15
exp_cond_cdf <- function(x) {
(pexp(42 - x, 1 / onset, lower.tail = FALSE) - pexp(t_max, 1 / onset, lower.tail = FALSE)) / pexp(t_max, 1 / onset)
}
} else {
exp_cond_cdf <- function(x) {
1 - (pexp(x, 1 / onset, lower.tail = FALSE) - pexp(t_max, 1 / onset, lower.tail = FALSE)) / pexp(t_max, 1 / onset)
}
}Here the the dose escalation designs are defined: in this example the TITE-CRM is used. Similarly the code can be adapted for the rolling-CRM.
library(crmPack)
t_max <- 42
model <- TITELogisticLogNormal(
mean = c(1.33, 1.49),
cov = matrix(c(1.826, 0.0209, 0.0209, 0.0245), nrow = 2),
ref_dose = refDose
)
myIncrements <- IncrementsRelative(
intervals = c(0, 20),
increments = c(10, 3)
)
myNextBest <- NextBestMTD(
target = 0.3,
derive =
function(mtd_samples) {
mean(mtd_samples)
}
)
myStopping <- StoppingMinPatients(nPatients = 48)
mySize <- CohortSizeConst(size = 3)
emptydata <- DataDA(doseGrid = seq(from = 2, to = 50, by = 2), Tmax = t_max)
mysafetywindow <- SafetyWindowConst(c(7, 7), 7, 7)
design <- DADesign(
model = model,
increments = myIncrements,
nextBest = myNextBest,
stopping = myStopping,
cohort_size = mySize,
data = emptydata,
safetyWindow = mysafetywindow,
startingDose = 8
)In order to obtain stable results, increase the simulation parameters appropriately (step, samples, nsim).
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.