tsegest {trtswitch}R Documentation

The Two-Stage Estimation (TSE) Method Using g-estimation for Treatment Switching

Description

Obtains the causal parameter estimate of the logistic regression switching model and the hazard ratio estimate of the Cox model to adjust for treatment switching.

Usage

tsegest(
  data,
  id = "id",
  stratum = "",
  tstart = "tstart",
  tstop = "tstop",
  event = "event",
  treat = "treat",
  censor_time = "censor_time",
  pd = "pd",
  pd_time = "pd_time",
  swtrt = "swtrt",
  swtrt_time = "swtrt_time",
  swtrt_time_upper = "",
  base_cov = "",
  conf_cov = "",
  low_psi = -3,
  hi_psi = 3,
  n_eval_z = 100,
  strata_main_effect_only = TRUE,
  firth = FALSE,
  flic = FALSE,
  recensor = TRUE,
  admin_recensor_only = TRUE,
  swtrt_control_only = TRUE,
  alpha = 0.05,
  ties = "efron",
  tol = 1e-06,
  boot = TRUE,
  n_boot = 1000,
  seed = NA
)

Arguments

data

The input data frame that contains the following variables:

  • id: The id to identify observations belonging to the same subject for counting process data with time-dependent covariates.

  • stratum: The stratum.

  • tstart: The starting time of the time interval for counting-process data with time-dependent covariates.

  • tstop: The stopping time of the time interval for counting-process data with time-dependent covariates.

  • event: The event indicator, 1=event, 0=no event.

  • treat: The randomized treatment indicator, 1=treatment, 0=control.

  • censor_time: The administrative censoring time. It should be provided for all subjects including those who had events.

  • pd: The disease progression indicator, 1=PD, 0=no PD.

  • pd_time: The time from randomization to PD.

  • swtrt: The treatment switch indicator, 1=switch, 0=no switch.

  • swtrt_time: The time from randomization to treatment switch.

  • swtrt_time_upper: The upper bound of treatment switching time.

  • base_cov: The baseline covariates (excluding treat).

  • conf_cov: The confounding variables for predicting treatment switching (excluding treat).

id

The name of the id variable in the input data.

stratum

The name(s) of the stratum variable(s) in the input data.

tstart

The name of the tstart variable in the input data.

tstop

The name of the tstop variable in the input data.

event

The name of the event variable in the input data.

treat

The name of the treatment variable in the input data.

censor_time

The name of the censor_time variable in the input data.

pd

The name of the pd variable in the input data.

pd_time

The name of the pd_time variable in the input data.

swtrt

The name of the swtrt variable in the input data.

swtrt_time

The name of the swtrt_time variable in the input data.

swtrt_time_upper

The name of the swtrt_time_upper variable in the input data.

base_cov

The names of baseline covariates (excluding treat) in the input data for the Cox model.

conf_cov

The names of confounding variables (excluding treat) in the input data for the logistic regression switching model.

low_psi

The lower limit of the causal parameter.

hi_psi

The upper limit of the causal parameter.

n_eval_z

The number of points between low_psi and hi_psi (inclusive) at which to evaluate the Wald statistics for the coefficient of the counterfactual in the logistic regression switching model.

strata_main_effect_only

Whether to only include the strata main effects in the logistic regression switching model. Defaults to TRUE, otherwise all possible strata combinations will be considered in the switching model.

firth

Whether the Firth's bias reducing penalized likelihood should be used. The default is FALSE.

flic

Whether to apply intercept correction to obtain more accurate predicted probabilities. The default is FALSE.

recensor

Whether to apply recensoring to counterfactual survival times. Defaults to TRUE.

admin_recensor_only

Whether to apply recensoring to administrative censoring times only. Defaults to TRUE. If FALSE, recensoring will be applied to the actual censoring times for dropouts.

swtrt_control_only

Whether treatment switching occurred only in the control group.

alpha

The significance level to calculate confidence intervals.

ties

The method for handling ties in the Cox model, either "breslow" or "efron" (default).

tol

The desired accuracy (convergence tolerance) for psi.

boot

Whether to use bootstrap to obtain the confidence interval for hazard ratio. Defaults to TRUE.

n_boot

The number of bootstrap samples.

seed

The seed to reproduce the bootstrap results. The seed from the environment will be used if left unspecified.

Details

We use the following steps to obtain the hazard ratio estimate and confidence interval had there been no treatment switching:

Value

A list with the following components:

Author(s)

Kaifeng Lu, kaifenglu@gmail.com

References

NR Latimer, IR White, K Tilling, and U Siebert. Improved two-stage estimation to adjust for treatment switching in randomised trials: g-estimation to address time-dependent confounding. Statistical Methods in Medical Research. 2020;29(10):2900-2918.

Examples


# Example 1: one-way treatment switching (control to active)

sim1 <- tsegestsim(
  n = 500, allocation1 = 2, allocation2 = 1, pbprog = 0.5, 
  trtlghr = -0.5, bprogsl = 0.3, shape1 = 1.8, 
  scale1 = 0.000025, shape2 = 1.7, scale2 = 0.000015, 
  pmix = 0.5, admin = 5000, pcatnotrtbprog = 0.5, 
  pcattrtbprog = 0.25, pcatnotrt = 0.2, pcattrt = 0.1, 
  catmult = 0.5, tdxo = 1, ppoor = 0.1, pgood = 0.04, 
  ppoormet = 0.4, pgoodmet = 0.2, xomult = 1.4188308, 
  milestone = 546, swtrt_control_only = TRUE,
  outputRawDataset = 1, seed = 2000)
  
fit1 <- tsegest(
  data = sim1$paneldata, id = "id", 
  tstart = "tstart", tstop = "tstop", event = "died", 
  treat = "trtrand", censor_time = "censor_time", 
  pd = "progressed", pd_time = "timePFSobs", swtrt = "xo", 
  swtrt_time = "xotime", swtrt_time_upper = "xotime_upper",
  base_cov = "bprog", conf_cov = "bprog*catlag", 
  low_psi = -3, hi_psi = 3, strata_main_effect_only = TRUE,
  recensor = TRUE, admin_recensor_only = TRUE, 
  swtrt_control_only = TRUE, alpha = 0.05, ties = "efron", 
  tol = 1.0e-6, boot = FALSE)
  
c(fit1$hr, fit1$hr_CI)

# Example 2: two-way treatment switching

sim2 <- tsegestsim(
  n = 500, allocation1 = 2, allocation2 = 1, pbprog = 0.5, 
  trtlghr = -0.5, bprogsl = 0.3, shape1 = 1.8, 
  scale1 = 0.000025, shape2 = 1.7, scale2 = 0.000015, 
  pmix = 0.5, admin = 5000, pcatnotrtbprog = 0.5, 
  pcattrtbprog = 0.25, pcatnotrt = 0.2, pcattrt = 0.1, 
  catmult = 0.5, tdxo = 1, ppoor = 0.1, pgood = 0.04, 
  ppoormet = 0.4, pgoodmet = 0.2, xomult = 1.4188308, 
  milestone = 546, swtrt_control_only = FALSE,
  outputRawDataset = 1, seed = 2000)
  
fit2 <- tsegest(
  data = sim2$paneldata, id = "id", 
  tstart = "tstart", tstop = "tstop", event = "died", 
  treat = "trtrand", censor_time = "censor_time", 
  pd = "progressed", pd_time = "timePFSobs", swtrt = "xo", 
  swtrt_time = "xotime", swtrt_time_upper = "xotime_upper",
  base_cov = "bprog", conf_cov = "bprog*catlag", 
  low_psi = -3, hi_psi = 3, strata_main_effect_only = TRUE,
  recensor = TRUE, admin_recensor_only = TRUE, 
  swtrt_control_only = FALSE, alpha = 0.05, ties = "efron", 
  tol = 1.0e-6, boot = FALSE)
  
c(fit2$hr, fit2$hr_CI)


[Package trtswitch version 0.1.1 Index]