Generalized triple outcome decision-making in basket trials.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY Journal of Biopharmaceutical Statistics Pub Date : 2025-01-02 Epub Date: 2024-01-02 DOI:10.1080/10543406.2023.2296054
Miao Zang, Rui Liu
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Abstract

Making the go/no-go decision is critical in Phase II (or Ib) clinical trials. The conventional decision-making framework based on a binary hypothesis testing has been gradually replaced by the TODeM (Triple Outcome Decision-Making) which has three zones of outcomes: go, no-go, and consider. The TODeM provides more flexibility in decision-making with considering both of statistical significance and clinical relevance. However, Bayesian methods (e.g. EXNEX, MUCE, etc.) for the information borrowing are still based on the binary decision-making framework. We propose a new decision-making process G-TODeM (Generalized Triple Outcome Decision-Making) to apply those Bayesian methods with information borrowing across different cohorts to the TODeM framework. Essentially, the information borrowed from other cohorts can shrink the consider zone of the inference cohort.

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篮子试验中的通用三重结果决策。
在 II 期(或 Ib 期)临床试验中,决定是否进行试验至关重要。基于二元假设检验的传统决策框架已逐渐被 TODeM(三重结果决策)所取代。TODeM 为决策提供了更大的灵活性,既考虑了统计意义,又考虑了临床相关性。然而,用于信息借用的贝叶斯方法(如 EXNEX、MUCE 等)仍基于二元决策框架。我们提出了一种新的决策过程 G-TODeM(广义三重结果决策),将这些具有不同队列信息借用功能的贝叶斯方法应用于 TODeM 框架。从本质上讲,从其他队列借用的信息可以缩小推理队列的考虑区域。
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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
期刊介绍: The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers: Drug, device, and biological research and development; Drug screening and drug design; Assessment of pharmacological activity; Pharmaceutical formulation and scale-up; Preclinical safety assessment; Bioavailability, bioequivalence, and pharmacokinetics; Phase, I, II, and III clinical development including complex innovative designs; Premarket approval assessment of clinical safety; Postmarketing surveillance; Big data and artificial intelligence and applications.
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