Evidence map›Paper›PMID 42220254›Full record

ArticleStatistical methods in medical research2026

Bayesian adaptive design for clinical trials with potential subgroup effects.

Xuekui Zhang, Qianyun Zhao, Cong Chen, Belaid Moa, Shelley Gao

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Xuekui ZhangDepartment of Mathematics and Statistics, University of Victoria, BC, Canada.ORCID 0000-0003-4728-2343
Qianyun ZhaoDepartment of Mathematics and Statistics, University of Victoria, BC, Canada.
Cong ChenBiostatistics and Research Decision Sciences, Merck & Co. Inc., Kenilworth, NJ, USA.
Belaid MoaDigital Research Alliance of Canada, Victoria, BC, Canada.
Shelley GaoDepartment of Mathematics and Statistics, University of Victoria, BC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adaptive clinical trial designs increasingly aim to improve efficiency while accommodating subgroup heterogeneity, yet most existing methods fix assumptions about drug efficacy and subgroup effects. We propose a Bayesian adaptive design that explicitly models and learns from uncertainty in both components. A hierarchical mixture prior represents uncertainty about overall treatment efficacy and the magnitude of a biomarker-defined subgroup effect. Interim data are used to update these hyperparameters into posterior distributions, enabling a decision-theoretic framework that adaptively selects the optimal testing strategy among three options: continuing with the overall population, focusing on the subgroup, or conducting a joint test of both. When joint testing is chosen, the posterior information further determines the optimal allocation of Type I error between populations by selecting an evidence-based

Indexed as

Adaptive Clinical Trials as TopicClinical Trials as TopicResearch DesignBayes TheoremComputer SimulationHumansModels, StatisticalMonte Carlo MethodTreatment Effect Heterogeneityalpha allocationBayesian adaptive designclinical trialdecision-theoretic clinical trial designGPU-accelerationType I error control

Identifiers

PMID42220254
PMCPMC13342478

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.