TODO: A Triple‐Outcome Double‐Criterion Optimal Design for Dose Monitoring‐and‐Optimization in Multi‐Dose Randomized Trials
Jingyi Zhang, Heng Zhou, Nolan A. Wages, Zifang Guo, Fang Liu, Thomas Jemielita, Fangrong Yan, Ruitao Lin

TL;DR
This paper introduces a new Bayesian statistical design for multi-dose cancer trials to improve dose monitoring and optimize drug development.
Contribution
A novel Bayesian two-stage design with triple-outcome decision rules for dose monitoring and optimization in multi-dose trials.
Findings
The proposed design uses dual criteria for dose admissibility and desirability.
A systematic calibration algorithm optimizes sample size and posterior probability cutoffs.
Simulation studies show robust performance across various scenarios.
Abstract
Detecting the efficacy signal and determining the optimal dose are critical steps to increase the probability of success and expedite the drug development in cancer treatment. After identifying a safe dose range through phase I studies, conducting a multidose randomized trial becomes an effective approach to achieve this objective. However, there have been limited formal statistical designs for such multidose trials, and dose selection in practice is often ad hoc, relying on descriptive statistics. We propose a Bayesian optimal two‐stage design to facilitate rigorous dose monitoring and optimization. Utilizing a flexible Bayesian dynamic linear model for the dose–response relationship, we employ dual criteria to assess dose admissibility and desirability. Additionally, we introduce a triple‐outcome trial decision procedure to consider dose selection beyond clinical factors. Under the…
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Taxonomy
TopicsStatistical Methods in Clinical Trials · Optimal Experimental Design Methods · Health Systems, Economic Evaluations, Quality of Life
