Bayesian Uncertainty Directed Trial Designs

Steffen Ventz, Matteo Cellamare, Sergio Bacallado, Lorenzo Trippa

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Most Bayesian response-adaptive designs unbalance randomization rates toward the most promising arms with the goal of increasing the number of positive treatment outcomes during the study, even though the primary aim of the trial is different. We discuss Bayesian uncertainty directed designs (BUD), a class of Bayesian designs in which the investigator specifies an information measure tailored to the experiment. All decisions during the trial are selected to optimize the available information at the end of the study. The approach can be applied to several designs, ranging from early stage multi-arm trials to biomarker-driven and multi-endpoint studies. We discuss the asymptotic limit of the patient allocation proportion to treatments, and illustrate the finite-sample operating characteristics of BUD designs through examples, including multi-arm trials, biomarker-stratified trials, and trials with multiple co-primary endpoints. Supplementary materials for this article, including a standardized description of the materials available for reproducing the work, are available as an online supplement.

Original languageEnglish (US)
Pages (from-to)962-974
Number of pages13
JournalJournal of the American Statistical Association
Volume114
Issue number527
DOIs
StatePublished - Jul 3 2019
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2018, © 2018 American Statistical Association.

Keywords

  • Decision theory
  • Information theory
  • Multi-arm clinical trials
  • Response-adaptive designs

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