4.6 Article

Evaluating Bayesian adaptive randomization procedures with adaptive clip methods for multi-arm trials

Journal

STATISTICAL METHODS IN MEDICAL RESEARCH
Volume 30, Issue 5, Pages 1273-1287

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/0962280221995961

Keywords

Adaptive clip method; adaptive randomization; multi-arm trials; patient horizon; utility

Funding

  1. Medical Research Council in the United Kingdom [MR/N028171/1, CA016672, CA221703]
  2. National Cancer Institute in the United States
  3. MRC [MR/N028171/1] Funding Source: UKRI

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Bayesian adaptive randomization is a method that adjusts random assignment based on data trends, but there is a risk of patients being assigned to inferior treatment arms. Researchers have proposed an adaptive clip method and utility approach to address these issues and aid in selecting a randomization procedure.
Bayesian adaptive randomization is a heuristic approach that aims to randomize more patients to the putatively superior arms based on the trend of the accrued data in a trial. Many statistical aspects of this approach have been explored and compared with other approaches; yet only a limited number of works has focused on improving its performance and providing guidance on its application to real trials. An undesirable property of this approach is that the procedure would randomize patients to an inferior arm in some circumstances, which has raised concerns in its application. Here, we propose an adaptive clip method to rectify the problem by incorporating a data-driven function to be used in conjunction with Bayesian adaptive randomization procedure. This function aims to minimize the chance of assigning patients to inferior arms during the early time of the trial. Moreover, we propose a utility approach to facilitate the selection of a randomization procedure. A cost that reflects the penalty of assigning patients to the inferior arm(s) in the trial is incorporated into our utility function along with all patients benefited from the trial, both within and beyond the trial. We illustrate the selection strategy for a wide range of scenarios.

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