
FusionForests is an R package for Bayesian tree
ensemble models for data fusion and causal
inference. The main model, FusionForest(),
combines data from a randomised controlled trial (RCT) and an
observational study (real-world data, RWD) in a single Bayesian
framework. Crucially, the observational data are not
assumed to be unconfounded.
The model targets heterogeneous treatment effects on continuous and (interval-)censored survival outcomes. Using an accelerated failure time specification, the outcome is decomposed over separate tree forests:
\[\log T = m_0^{\mathrm{sh}}(X) + (1-S)\,d(X) + A\,\tau(X) + (1-S)\,A\,c(X) + \varepsilon,\]
where \(T\) is the survival time (for a continuous outcome, \(\log T\) is replaced by the outcome itself), \(A\) is the treatment, \(S\) indicates the source (\(S = 1\) for the RCT, \(S = 0\) for the RWD), and \(\varepsilon\) is a mean-zero error term — Gaussian or a flexible Dirichlet-process mixture. Each term is modelled by its own forest:
control
arguments);deviation arguments);treat
arguments);deconf arguments).The real-world data alone identify only the sum \(\tau(x) + c(x)\). The trial anchors \(\tau\), so the observational data add precision without their confounding leaking into the treatment effect estimate.
The methodology is described in:
Bayesian fusion forests for heterogeneous treatment effects on survival from randomised and real-world data T. Jacobs, S.L. van der Pas, W.N. van Wieringen https://arxiv.org/abs/2607.29295
Install the released version from CRAN:
install.packages("FusionForests")The development version can be installed from GitHub:
# install.packages("remotes")
remotes::install_github("tijn-jacobs/FusionForests")A small RCT (n = 200) is combined with a larger RWD cohort (n = 800)
in which treatment assignment depends on an unobserved
confounder U that also affects survival:
library(FusionForests)
set.seed(42)
n_rct <- 200
n_rwd <- 800
n <- n_rct + n_rwd
X <- matrix(rnorm(n * 3), n, 3)
U <- rnorm(n) # unobserved confounder
s <- rep(c(1, 0), c(n_rct, n_rwd)) # 1 = RCT, 0 = RWD
# Treatment: randomised in the RCT, driven by U in the RWD
a <- ifelse(s == 1,
rbinom(n, 1, 0.5),
rbinom(n, 1, plogis(1.5 * U)))
# True heterogeneous effect on log survival time
tau <- 0.4 + 0.4 * X[, 1]
log_t <- 1 + X[, 1] + 0.5 * X[, 2] + a * tau + 0.7 * U + 0.3 * rnorm(n)
true_time <- exp(log_t)
cens_time <- rexp(n, rate = 1 / (2 * mean(true_time)))
time <- pmin(true_time, cens_time)
status <- as.integer(true_time <= cens_time)
fit <- FusionForest(
y = time, status = status,
X_train_control = X, X_train_treat = X,
treatment_indicator_train = a, source_indicator_train = s,
X_test_control = X, X_test_treat = X,
treatment_indicator_test = a, source_indicator_test = s,
outcome_type = "right-censored",
N_post = 2000, N_burn = 2000,
store_posterior_sample = TRUE
)
# Posterior draws of the treatment effect (log-time scale) per subject
cate <- log(fusion_estimand(fit, estimand = "AF"))
cate_mean <- colMeans(cate)
cate_lo <- apply(cate, 2, quantile, 0.025)
cate_hi <- apply(cate, 2, quantile, 0.975)
plot(tau, cate_mean, pch = 19, cex = 0.45, col = "#2a78d6",
xlab = "True treatment effect (log-time scale)",
ylab = "Posterior treatment effect")
segments(tau, cate_lo, tau, cate_hi, col = adjustcolor("#2a78d6", 0.12))
abline(0, 1, lty = 2, col = "grey40")
Even though treatment assignment in the RWD is driven by an unobserved confounder, the fitted treatment effects track the truth (correlation 0.89) and the 95% credible intervals cover the true effect for 94% of subjects.
The vignette walks through a complete analysis of the semi-synthetic
breast_fusion data, which ship with the package. It covers
the model fit, single-source comparisons, causal estimands, posterior
projections, the confounding function and the error model. Open it in R
with:
vignette("FusionForests")It is also available on CRAN.
FusionForest() is the heart of the package. It fits the
decomposition above with standard BART priors on each forest and returns
posterior draws of every component, so treatment effects, source
deviations and uncertainty are all available directly from one fit.
Right-censored and interval-censored survival outcomes are handled
through data augmentation, and the error distribution can be Gaussian or
a Dirichlet-process mixture (error_dist) for added
robustness.
Two companion functions summarise a fit:
fusion_estimand() returns posterior draws of causal
survival estimands (survival difference, acceleration factor), and
fusion_projection() projects the treatment effect surface
onto an interpretable linear basis.
The single-study causal and survival models from the ShrinkageTrees
package are re-exported, so library(FusionForests) provides
every model from the accompanying paper in one namespace.
This project has received funding from the European Research Council (ERC) under the European Union’s Horizon Europe program under Grant agreement No. 101074802. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Research Council Executive Agency. Neither the European Union nor the granting authority can be held responsible for them. This work used the Dutch national e-infrastructure with the support of the SURF Cooperative using grant no. EINF-18803.