A Bayesian Precision Response-adaptive Phase II Clinical Trial Design for Radiotherapies with Competing Risk Survival Outcomes
Jina Park, Wenjing Hu, Ick Hoon Jin, Hao Liu, Yong Zang

TL;DR
This paper introduces a Bayesian adaptive trial design for radiotherapy that accounts for competing risks and patient heterogeneity, enabling personalized dose evaluation and improved treatment efficacy.
Contribution
It develops a novel Bayesian precision phase II trial methodology incorporating competing risks and subgroup-specific effects for radiotherapy.
Findings
The proposed design outperforms traditional methods in simulations.
Personalized dosing improves patient outcomes.
Adaptive randomization favors more effective doses.
Abstract
Many phase II clinical trials have used survival outcomes as the primary endpoints in recent decades. Suppose the radiotherapy is evaluated in a phase II trial using survival outcomes. In that case, the competing risk issue often arises because the time to disease progression can be censored by the time to normal tissue complications, and vice versa. Besides, much literature has examined that patients receiving the same radiotherapy dose may yield distinct responses due to their heterogeneous radiation susceptibility statuses. Therefore, the "one-dose-fit-all" strategy often fails, and it is more relevant to evaluate the subgroup-specific treatment effect with the subgroup defined by the radiation susceptibility status. In this paper, we propose a Bayesian precision phase II trial design evaluating the subgroup-specific treatment effects of radiotherapy. We use the cause-specific hazard…
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Taxonomy
TopicsStatistical Methods in Clinical Trials · Optimal Experimental Design Methods · Health Systems, Economic Evaluations, Quality of Life
