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Auxiliary variable-enriched biomarker-stratified design.辅助变量富集生物标志物分层设计。
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2
A simulation study of outcome adaptive randomization in multi-arm clinical trials.多臂临床试验中结局自适应随机化的模拟研究。
Clin Trials. 2017 Oct;14(5):432-440. doi: 10.1177/1740774517692302. Epub 2017 Feb 1.
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On Enrichment Strategies for Biomarker Stratified Clinical Trials.关于生物标志物分层临床试验的富集策略
J Biopharm Stat. 2018;28(2):292-308. doi: 10.1080/10543406.2017.1379532. Epub 2017 Oct 30.
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Adaptive Clinical Trials: Advantages and Disadvantages of Various Adaptive Design Elements.适应性临床试验:各种适应性设计要素的优缺点
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Interim decision-making strategies in adaptive designs for population selection using time-to-event endpoints.使用事件发生时间终点进行群体选择的适应性设计中的临时决策策略。
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EGFR mutation incidence in non-small-cell lung cancer of adenocarcinoma histology: a systematic review and global map by ethnicity (mutMapII).非小细胞肺癌中腺癌组织学的 EGFR 突变发生率:按种族的系统评价和全球图谱(mutMapII)。
Am J Cancer Res. 2015 Aug 15;5(9):2892-911. eCollection 2015.
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Probability estimation with machine learning methods for dichotomous and multicategory outcome: applications.使用机器学习方法进行二分类和多分类结果的概率估计:应用
Biom J. 2014 Jul;56(4):564-83. doi: 10.1002/bimj.201300077. Epub 2014 Feb 12.
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Tumour heterogeneity and cancer cell plasticity.肿瘤异质性和癌细胞可塑性。
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Adaptive adjustment of the randomization ratio using historical control data.利用历史对照数据进行随机化比例的适应性调整。
Clin Trials. 2013;10(3):430-40. doi: 10.1177/1740774513483934.
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Adaptive enrichment designs for clinical trials.临床试验的适应性富集设计。
Biostatistics. 2013 Sep;14(4):613-25. doi: 10.1093/biostatistics/kxt010. Epub 2013 Mar 21.

一种采用贝叶斯自适应随机化的特征富集设计。

A Signature Enrichment Design with Bayesian Adaptive Randomization.

作者信息

Xia Fang, George Stephen L, Ning Jing, Li Liang, Huang Xuelin

机构信息

Department of Biostatistics, The University of Texas MD Anderson Cancer Center.

Department of Biostatistics and Bioinformatics, Duke University School of Medicine.

出版信息

J Appl Stat. 2021;48(6):1091-1110. doi: 10.1080/02664763.2020.1757048. Epub 2020 Apr 27.

DOI:10.1080/02664763.2020.1757048
PMID:34024982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8132854/
Abstract

Clinical trials in the era of precision cancer medicine aim to identify and validate biomarker signatures which can guide the assignment of individually optimal treatments to patients. In this article, we propose a group sequential randomized phase II design, which updates the biomarker signature as the trial goes on, utilizes enrichment strategies for patient selection, and uses Bayesian response-adaptive randomization for treatment assignment. To evaluate the performance of the new design, in addition to the commonly considered criteria of type I error and power, we propose four new criteria measuring the benefits and losses for individuals both inside and outside of the clinical trial. Compared with designs with equal randomization, the proposed design gives trial participants a better chance to receive their personalized optimal treatments and thus results in a higher response rate on the trial. This design increases the chance to discover a successful new drug by an adaptive enrichment strategy, i.e., identification and selective enrollment of a subset of patients who are sensitive to the experimental therapies. Simulation studies demonstrate these advantages of the proposed design. It is illustrated by an example based on an actual clinical trial in non-small-cell lung cancer.

摘要

精准癌症医学时代的临床试验旨在识别和验证生物标志物特征,以指导为患者分配个体化的最佳治疗方案。在本文中,我们提出了一种成组序贯随机II期设计,该设计在试验进行过程中更新生物标志物特征,采用富集策略进行患者选择,并使用贝叶斯反应自适应随机化进行治疗分配。为了评估新设计的性能,除了常用的I型错误和检验效能标准外,我们还提出了四个新的标准,用于衡量临床试验内外个体的收益和损失。与等随机化设计相比,所提出的设计使试验参与者有更好的机会接受个性化的最佳治疗,从而在试验中获得更高的缓解率。这种设计通过自适应富集策略增加了发现成功新药的机会,即识别和选择性招募对实验性治疗敏感的患者亚组。模拟研究证明了所提出设计的这些优势。通过一个基于非小细胞肺癌实际临床试验的例子进行了说明。