hist_SA {OncoBayes2}R Documentation

Single-agent example

Description

Example data from the application in Neuenschwander, et. al. 2008, from an "open-label, multicenter, non-comparative, dose-escalation cancer trial to characterize the safety, tolerability, and pharmacokinetic profile of a drug and to determine its MTD."

Usage

hist_SA

Format

A data frame with 5 rows and 4 variables:

group_id

study

drug_A

dose

num_patients

number of patients

num_toxicities

number of events

References

Neuenschwander, B., Branson, M., & Gsponer, T. (2008). Critical aspects of the Bayesian approach to phase I cancer trials. Statistics in medicine, 27(13), 2420-2439.

Examples

## Setting up dummy sampling for fast execution of example
## Please use 4 chains and 100x more warmup & iter in practice
.user_mc_options <- options(OncoBayes2.MC.warmup=10, OncoBayes2.MC.iter=20, OncoBayes2.MC.chains=1,
                            OncoBayes2.MC.save_warmup=FALSE)

## Example from Neuenschwander, B., et al. (2009). Stats in Medicine

num_comp <- 1 # one investigational drug
num_inter <- 0 # no drug-drug interactions need to be modeled
num_groups <- nlevels(hist_SA$group_id) # no stratification needed
num_strata <- 1 # no stratification needed


dref <- 50

## Since there is no prior information the hierarchical model
## is not used in this example by setting tau to (almost) 0.
blrmfit <- blrm_exnex(
  cbind(num_toxicities, num_patients - num_toxicities) ~
    1 + log(drug_A / dref) |
    0 |
    group_id,
  data = hist_SA,
  prior_EX_mu_mean_comp = matrix(
    c(logit(1/2), # mean of intercept on logit scale
      log(1)),    # mean of log-slope on logit scale
    nrow = num_comp,
    ncol = 2
  ),
  prior_EX_mu_sd_comp = matrix(
    c(2,  # sd of intercept
      1), # sd of log-slope
    nrow = num_comp,
    ncol = 2
  ),
  ## Here we take tau as known and as zero.
  ## This disables the hierarchical prior which is
  ## not required in this example as we analyze a
  ## single trial.
  prior_EX_tau_mean_comp = matrix(
    c(0, 0),
    nrow = num_comp,
    ncol = 2
  ),
  prior_EX_tau_sd_comp = matrix(
    c(1, 1),
    nrow = num_comp,
    ncol = 2
  ),
  prior_EX_prob_comp = matrix(1, nrow = num_comp, ncol = 1),
  prior_tau_dist = 0,
  prior_PD = FALSE
)
## Recover user set sampling defaults
options(.user_mc_options)


[Package OncoBayes2 version 0.8-9 Index]