基于分层贝叶斯约束模型的潜伏亚组篮式试验设计。

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Kentaro Takeda, Atsuki Hashimoto, Shufang Liu, Alan Rong
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引用次数: 0

摘要

众所周知,由多种癌症类型组成的 "篮子 "试验有可能在癌症类型定义的 "篮子 "之间借力,从而在样本量和试验持续时间方面实现高效设计。这些篮子中的治疗效果通常是异质的,并按癌症类型对治疗敏感或不敏感进行分类。因此,许多现有篮子试验中的可交换性假设可能会被违反,因此有必要在设计试验时取消这一假设。本文简化了两个分类器的受限分层贝叶斯模型(CHBM-LS),以处理癌症类型单一分类器导致的治疗效果潜在异质性。使用潜子群建模方法将不同的篮子聚合成子群。治疗效果具有相似性和可交换性,以便于在每个潜在子组内进行信息借用。将简化的 CHBM-LS 方法应用到仅由癌症类型定义篮子的实际篮子试验中,显示出比其他可用方法更好的性能。进一步的模拟研究还表明,在各种情况下,CHBM-LS 方法都优于其他方法,具有更高的统计功率和更好的 I 类错误率控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A basket trial design based on constrained hierarchical Bayesian model for latent subgroups.

It is well known a basket trial consisting of multiple cancer types has the potential of borrowing strength across the baskets defined by the cancer types, leading to an efficient design in terms of sample size and trial duration. The treatment effects in those baskets are often heterogeneous and categorized by the cancer types being sensitive or insensitive to the treatment. Hence, the assumption of exchangeability in many existing basket trials may be violated, and there is a need to design trials without this assumption. In this paper, we simplify the constrained hierarchical Bayesian model for latent subgroups (CHBM-LS) for two classifiers to deal with the potential heterogeneity of treatment effects due to the single classifier of the cancer type. Different baskets are aggregated into subgroups using a latent subgroup modeling approach. The treatment effects are similar and exchangeable to facilitate information borrowing within each latent subgroup. Applying the simplified CHBM-LS approach to the real basket trials where baskets defined by only cancer types shows better performance than other available approaches. Further simulation study also demonstrates this CHBM-LS approach outperforms other approaches with higher statistical power and better-controlled type I error rates under various scenarios.

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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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