## 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
)
dref <- c(6, 960)
num_comp <- 2 # two investigational drugs
num_inter <- 1 # one drug-drug interaction needs to be modeled
num_groups <- nlevels(codata_combo2$group_id) # no stratification needed
num_strata <- 1 # no stratification needed
blrmfit <- blrm_exnex(
cbind(num_toxicities, num_patients - num_toxicities) ~
1 + I(log(drug_A / dref[1])) |
1 + I(log(drug_B / dref[2])) |
0 + I(drug_A / dref[1] * drug_B / dref[2]) |
group_id,
data = codata_combo2,
prior_EX_mu_comp = list(mixmvnorm(c(1, logit(0.2), 0, diag(c(2^2, 1)))),
mixmvnorm(c(1, logit(0.2), 0, diag(c(2^2, 1))))),
prior_EX_tau_comp = list(mixmvnorm(c(1,
log(0.250), log(0.125),
diag(c(log(4)/1.96, log(4)/1.96)^2))),
mixmvnorm(c(1,
log(0.250), log(0.125),
diag(c(log(4)/1.96, log(4)/1.96)^2)))),
prior_EX_mu_inter = mixmvnorm(c(1, 0, 1.121^2)),
prior_EX_tau_inter = mixmvnorm(c(1, log(0.125), (log(4) / 1.96)^2)),
prior_is_EXNEX_comp = rep(FALSE, num_comp),
prior_is_EXNEX_inter = rep(FALSE, num_inter),
prior_EX_prob_comp = matrix(1, nrow = num_groups, ncol = num_comp),
prior_EX_prob_inter = matrix(1, nrow = num_groups, ncol = num_inter),
prior_tau_dist = 1
)
## Recover user set sampling defaults
options(.user_mc_options)
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