SAME (version 0.1.0)

sim.trial: Function to simulate Bayesian seamless multi-arm biomarker-enriched phase II/III designs

Description

This function finds the required number of events
using a multi-arm multi-stage biomarker-enriched design with time-to-event
endpoints.

Usage

sim.trial(
  median.c,
  hr,
  K,
  L,
  lfu,
  alpha,
  power,
  accrate,
  theta,
  bio.preva,
  FAtime.phase3,
  N.iter
)

Value

sim_trial() returns the nominal type I error rate and calibrated cutoff points, nominal power under user-defined hypothesis, empirical power under user-defined number of simulations, the duration of trial(time), the number of events (num_evs), the number of patients (num_pts) from different stages. The function can also display the number of events and patients under the selected subgroup, the distribution of decision zones and the estimated hazard ratio for the final analysis.

Arguments

median.c

The median survival time for control group

hr

Alternative hazard ratio

K

Number of biomarkers

L

Information fraction in terms of the accumulative events in phase II stage, e.g., K = c(1/4,1/2,1)

lfu

Follow-up time

alpha

One-sided familywise error rate

power

Power

accrate

Accrual rate

theta

A clinically meaningful treatment effect size defined by clinicians

bio.preva

Prevalence of biomarker(s)

FAtime.phase3

the study ending time of phase III

N.iter

Number of iterations

Examples

# \donttest{
sim.trial(median.c=12,hr=c(1,1,1,0.6),K=2,L=c(1/4,1/2,1),lfu=0,
          alpha=0.05,power=0.9,accrate=15,theta=log(1.25),
          bio.preva=c(0.4,0.6),FAtime.phase3=48,N.iter=5)
# }