Show the summary of the simulations
Source:R/Simulations-methods.R
show-SimulationsSummary-method.Rd
Show the summary of the simulations
Arguments
- object
the
SimulationsSummary
object we want to print
Examples
# nolint start
# Define the dose-grid
emptydata <- Data(doseGrid = c(1, 3, 5, 10, 15, 20, 25, 40, 50, 80, 100))
# Initialize the CRM model
model <- LogisticLogNormal(
mean = c(-0.85, 1),
cov =
matrix(c(1, -0.5, -0.5, 1),
nrow = 2
),
ref_dose = 56
)
# Choose the rule for selecting the next dose
myNextBest <- NextBestNCRM(
target = c(0.2, 0.35),
overdose = c(0.35, 1),
max_overdose_prob = 0.25
)
# Choose the rule for the cohort-size
mySize1 <- CohortSizeRange(
intervals = c(0, 30),
cohort_size = c(1, 3)
)
mySize2 <- CohortSizeDLT(
intervals = c(0, 1),
cohort_size = c(1, 3)
)
mySize <- maxSize(mySize1, mySize2)
# Choose the rule for stopping
myStopping1 <- StoppingMinCohorts(nCohorts = 3)
myStopping2 <- StoppingTargetProb(
target = c(0.2, 0.35),
prob = 0.5
)
myStopping3 <- StoppingMinPatients(nPatients = 20)
myStopping <- (myStopping1 & myStopping2) | myStopping3
# Choose the rule for dose increments
myIncrements <- IncrementsRelative(
intervals = c(0, 20),
increments = c(1, 0.33)
)
# Initialize the design
design <- Design(
model = model,
nextBest = myNextBest,
stopping = myStopping,
increments = myIncrements,
cohort_size = mySize,
data = emptydata,
startingDose = 3
)
## define the true function
myTruth <- probFunction(model, alpha0 = 7, alpha1 = 8)
# Run the simulation on the desired design
# We only generate 1 trial outcome here for illustration, for the actual study
# this should be increased of course
options <- McmcOptions(
burnin = 100,
step = 2,
samples = 1000
)
time <- system.time(mySims <- simulate(design,
args = NULL,
truth = myTruth,
nsim = 1,
seed = 819,
mcmcOptions = options,
parallel = FALSE
))[3]
# Show the Summary of the Simulations
show(summary(mySims, truth = myTruth))
#> Summary of 1 simulations
#>
#> Target toxicity interval was 20, 35 %
#> Target dose interval corresponding to this was 19.6, 21.6
#> Intervals are corresponding to 10 and 90 % quantiles
#>
#> Number of patients overall : mean 22 (22, 22)
#> Number of patients treated above target tox interval : mean 9 (9, 9)
#> Proportions of DLTs in the trials : mean 27 % (27 %, 27 %)
#> Mean toxicity risks for the patients on active : mean 28 % (28 %, 28 %)
#> Doses selected as MTD : mean 20 (20, 20)
#> True toxicity at doses selected : mean 22 % (22 %, 22 %)
#> Proportion of trials selecting target MTD: 100 %
#> Dose most often selected as MTD: 20
#> Observed toxicity rate at dose most often selected: 100 %
#> Fitted toxicity rate at dose most often selected : mean 27 % (27 %, 27 %)
#> Stop reason triggered:
#> ≥ 3 cohorts dosed : 100 %
#> P(0.2 ≤ prob(DLE | NBD) ≤ 0.35) ≥ 0.5 : 100 %
#> ≥ 20 patients dosed : 100 %
# nolint end