knitr::opts_chunk$set(
  collapse = TRUE,
  comment = "#>"
)

run <- requireNamespace("dplyr", quietly = TRUE) &&
  requireNamespace("gt", quietly = TRUE)
knitr::opts_chunk$set(eval = run)

Introduction

This vignette demonstrates use of a simple routine to do simulations and testing using Fleming-Harrington weighted logrank tests and the MaxCombo test. In addition, we demonstrate how to perform these tests with a dataset not generated by simulation routines within the package. Note that all $p$-values computed here are one-sided with small values indicating that the experimental treatment is favored.

Defining the test

The MaxCombo test has been posed as the maximum of multiple Fleming-Harrington weighted logrank tests (@FH1982, @FH2011). Combination tests looking at a maximum of selected tests in this class have also been proposed; see @Lee2007, @NPHWGDesign, and @NPHWGSimulation. The Fleming-Harrington class is indexed by the parameters $\rho \geq 0$ and $\gamma \geq 0$. We will denote these as FH($\rho, \gamma$). This class includes the logrank test as FH(0, 0). Other tests of interest here include:

Executing for a single dataset

Generating test statistics with sim_fixed_n()

We begin with a single trial simulation generated by the routine sim_fixed_n() using default arguments for that routine. sim_fixed_n() produces one record per test and data cutoff method per simulation. Here we choose 3 tests (logrank = FH(0, 0), FH(0, 1) and FH(1, 1)). When more than one test is chosen the correlation between tests is computed as shown by @Karrison2016, in this case in the columns V1, V2, V3. The columns rho, gamma indicate $\rho$ and $\gamma$ used to compute the test. z is the FH($\rho, \gamma$) normal test statistic with variance 1 with a negative value favoring experimental treatment. The variable cut indicates how the data were cut for analysis, in this case at the maximum of the targeted minimum follow-up after last enrollment and the date at which the targeted event count was reached. Sim is a sequential index of the simulations performed.

library(simtrial)
library(knitr)
library(dplyr)
library(gt)
set.seed(123)

x <- sim_fixed_n(
  n_sim = 1,
  timing_type = 5,
  rho_gamma = data.frame(rho = c(0, 0, 1), gamma = c(0, 1, 1))
)

x |>
  gt() |>
  fmt_number(columns = c("ln_hr", "z", "duration", "v1", "v2", "v3"), decimals = 2)

Generating data with sim_pw_surv()

We begin with another simulation generated by sim_pw_surv(). Again, we use defaults for that routine.

set.seed(123)

s <- sim_pw_surv(n = 100)

s |>
  head() |>
  gt() |>
  fmt_number(columns = c("enroll_time", "fail_time", "dropout_time", "cte"), decimals = 2)

Once generated, we need to cut the data for analysis. Here we cut after 75 events.

x <- s |> cut_data_by_event(75)

x |>
  head() |>
  gt() |>
  fmt_number(columns = "tte", decimals = 2)

Now we can analyze this data. We begin with s to show how this can be done in a single line. In this case, we use the 4 test combination suggested in @NPHWGSimulation, @NPHWGDesign.

z <- s |>
  cut_data_by_event(75) |>
  maxcombo(rho = c(0, 0, 1, 1), gamma = c(0, 1, 0, 1))

z

Suppose we want the $p$-value just based on the logrank and FH(0, 1) and FH(1, 0) as suggested by @Lee2007. We remove the rows and columns associated with FH(0, 0) and FH(1, 1) and then apply pvalue_maxcombo().

z <- s |>
  cut_data_by_event(75) |>
  maxcombo(rho = c(0, 1), gamma = c(1, 0))

z

Using survival data in another format

For a trial not generated by sim_fixed_n(), the process is slightly more involved. We consider survival data not in the simtrial format and show the transformation needed. In this case we use the small aml dataset from the survival package.

library(survival)
aml |>
  head() |>
  gt()

We rename variables and create a stratum variable as follows:

x <- aml |> transmute(
  tte = time,
  event = status,
  stratum = "All",
  treatment = case_when(
    x == "Maintained" ~ "experimental",
    x == "Nonmaintained" ~ "control"
  )
)

x |>
  head() |>
  gt()

Now we analyze the data with a MaxCombo with the logrank and FH(0, 1) and compute a $p$-value.

x |> maxcombo(rho = c(0, 0), gamma = c(0, 1))

Simulation

We now consider the example simulation from the pvalue_maxcombo() help file to demonstrate how to simulate power for the MaxCombo test. However, we increase the number of simulations to 100 in this case; a larger number should be used (e.g., 1000) for a better estimate of design properties. Here we will test at the $\alpha=0.001$ level.

set.seed(123)

# Only use cut events + min follow-up
x <- sim_fixed_n(
  n_sim = 100,
  timing_type = 5,
  rho_gamma = data.frame(rho = c(0, 0, 1), gamma = c(0, 1, 1))
)

# MaxCombo power estimate for cutoff at max of targeted events, minimum follow-up
x |>
  group_by(sim) |>
  filter(row_number() == 1) |>
  ungroup() |>
  summarize(power = mean(p_value < .001))

We note the use of group_map in the above produces a list of $p$-values for each simulation. It would be nice to have something that worked more like dplyr::summarize() to avoid unlist() and to allow evaluating, say, multiple data cutoff methods. The latter can be done without having to re-run all simulations as follows, demonstrated with a smaller number of simulations.

# Only use cuts for events and events + min follow-up
set.seed(123)

x <- sim_fixed_n(
  n_sim = 100,
  timing_type = c(2, 5),
  rho_gamma = data.frame(rho = 0, gamma = c(0, 1))
)

Now we compute a $p$-value separately for each cut type, first for targeted event count.

# Subset to targeted events cutoff tests
# This chunk will be updated after the development of sim_gs_n and sim_fixed_n
x |>
  filter(cut == "Targeted events") |>
  group_by(sim) |>
  filter(row_number() == 1) |>
  ungroup() |>
  summarize(power = mean(p_value < .025))

Now we use the later of targeted events and minimum follow-up cutoffs.

# Subset to targeted events cutoff tests
x |>
  filter(cut != "Targeted events") |>
  group_by(sim) |>
  filter(row_number() == 1) |>
  ungroup() |>
  summarize(power = mean(p_value < .025))

References



Merck/simtrial documentation built on April 14, 2025, 5:37 a.m.