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]