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BayesTSM fits Bayesian progressive three-state
semi-Markov models for screening panel data with censoring after
intervention. It is designed for settings where individuals are
repeatedly screened for a progressive disease process, for example:
The package models the latent transition time from baseline to state
2, denoted X, and the transition time from state 2 to state
3, denoted S. The total time from baseline to state 3 is
Y = X + S.
BayesTSM uses accelerated failure time models for both
transition times,
\[ \begin{aligned} \log X_i &= z_{Xi}^{\top}\beta_X + \sigma_X \epsilon_i, \\ \log S_i &= z_{Si}^{\top}\beta_S + \sigma_S \xi_i . \end{aligned} \]
and estimates the model using Bayesian data augmentation and MCMC. Weibull, lognormal, and log-logistic transition time distributions are currently available.
Install the development version from GitHub with:
# install.packages("devtools")
devtools::install_github(
"thomasklausch2/BayesTSM",
build_vignettes = TRUE
)library(BayesTSM)
set.seed(1)
dat <- gendat(
n = 1000,
p = 2,
sigma.X = 0.3,
mu.X = 2,
beta.X = c(0.5, 0.5),
sigma.S = 0.5,
mu.S = 1,
beta.S = c(0.5, 0.5),
dist.X = "weibull",
dist.S = "weibull",
v.min = 1,
v.max = 5,
Tmax = 200,
mean.rc = 10
)
head(dat)
table(dat$d)The variables passed to bayestsm() are:
d: event type, where 1 denotes right
censoring, 2 a pre-state event, and 3 a
terminal-state event;L: left bound of the final screening interval;R: right bound of the final screening interval, or
Inf for right-censored observations;Z.X: covariate matrix for the X transition
model;Z.S: covariate matrix for the S transition
model.d <- dat$d
L <- dat$L
R <- dat$R
Z <- dat[, c("Z.1", "Z.2")]
mod <- bayestsm(
d = d,
L = L,
R = R,
Z.X = Z,
Z.S = Z,
mc = 1e4,
warmup = 5e2,
thinning = 10,
chains = 4,
update_till_convergence = TRUE,
mc_update = 1e4,
MH = FALSE,
dist.X = "weibull",
dist.S = "weibull",
seed_chains = 1:4
)By default, BayesTSM uses slice sampling for the model
parameters. Metropolis sampling can be used instead by setting
MH = TRUE.
summary(mod, warmup = 500)
plot(mod, warmup = 500)The summary method reports posterior medians, 95% credible intervals, R-hat values, and effective sample sizes.
Posterior predictive cumulative transition probabilities can be
obtained with ppCIF().
ppCIF(
mod,
type = "quantiles",
warmup = 500,
quant = c(5, 10)
)For plotting cumulative transition probability curves:
pp_grid <- ppCIF(
mod,
type = "quantiles",
warmup = 500
)
plot(pp_grid, xlim = c(0, 50))Conditional predictions can be obtained by fixing covariate values
through fix_Z.X and fix_Z.S.
ppCIF(
mod,
type = "quantiles",
warmup = 500,
quant = c(5, 10),
fix_Z.X = c(1, NA),
fix_Z.S = c(1, NA)
)Here, the first covariate is fixed at 1, while the second covariate is marginalized over its observed distribution.
Different transition time distributions can be compared using information criteria.
get_IC(mod, warmup = 500, cores = NULL)get_IC() returns the deviance information criterion
(DIC) and two versions of the widely applicable information criterion
(WAIC-1 and WAIC-2).
Akwiwu, E. U., Coupé, V. M. H., Berkhof, J., & Klausch, T. (2026). A comparison of methods for modeling multistate cancer progression using screening data with censoring after intervention. Medical Decision Making. https://doi.org/10.1177/0272989X261422681
Klausch, T., Akwiwu, E. U., van de Wiel, M. A., Coupé, V. M. H., & Berkhof, J. (2023). A Bayesian accelerated failure time model for interval censored three-state screening outcomes. The Annals of Applied Statistics, 17(2), 1285–1306. https://doi.org/10.1214/22-AOAS1669
Vehtari, A., Gelman, A., Simpson, D., Carpenter, B., & Bürkner, P.-C. (2021). Rank-normalization, folding, and localization: An improved R-hat for assessing convergence of MCMC. Bayesian Analysis, 16(2), 667–718. https://doi.org/10.1214/20-BA1221
Watanabe, S. (2010). Asymptotic equivalence of Bayes cross validation and widely applicable information criterion in singular learning theory. Journal of Machine Learning Research, 11, 3571–3594.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.