Kristine Broglio, Freda Cooner, Yujun Wu, Mike Xiao, X Q Xue, Marina Lowen, Izuagie Ikhapoh, Philip He
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引用次数: 0
Abstract
Introduction: Although oncology has seen large scientific and clinical advances over the last decade, it also has one of the lowest success rates for novel agents across therapeutic areas. Adaptive clinical trial design has been a popular option for increasing clinical trial efficiency and the chances of trial success. Seamless clinical trial design are studies in which two or more clinical trial phases are combined into a single study with a pre-specified transition between stages. This integration of phases may enhance efficiency.
Methods: To understand the precedent for the use of seamless designs, this working group was formed to conduct a comprehensive literature search on seamless clinical trials conducted with confirmatory intent in oncology. Trial design features were extracted into a database and analyzed with descriptive statistics.
Results: A literature search identified 68 clinical trials meeting inclusion and exclusion criteria. The most common design feature was a gate on treatment efficacy, where the trial would only proceed to the second stage if sufficient efficacy was observed in the first. The next most common feature was a selection of a dose or treatment regimen. Inferentially and operationally seamless designs were approximately equally represented.
Discussion: Key statistical considerations for seamless phase II/III designs include optimizing design choices by evaluating and comparing operating characteristics across design alternatives as well as showing control of overall Type I error rates. Executing the transition between phases should be evaluated for issues related to accrual, drug production, and procedures to maintain trial integrity.
Conclusions: While there are unique statistical, regulatory, and operational considerations for seamless designs they are also uniquely suited to many development settings. These include, for example, addressing dose selection under FDA's Project Optimus and addressing the growing use of biomarkers and personalized medicine approaches in cancer treatment.
导言:尽管肿瘤学在过去十年中取得了巨大的科学和临床进步,但它也是所有治疗领域中新型药物成功率最低的领域之一。自适应临床试验设计一直是提高临床试验效率和试验成功几率的热门选择。无缝临床试验设计是指将两个或两个以上的临床试验阶段合并为一项研究,并预先规定阶段之间的过渡。这种阶段整合可提高效率:为了了解使用无缝设计的先例,我们成立了本工作组,对肿瘤学领域以确证为目的的无缝临床试验进行了全面的文献检索。将试验设计特点提取到数据库中,并进行描述性统计分析:文献检索发现了 68 项符合纳入和排除标准的临床试验。最常见的设计特征是疗效关,即只有在第一阶段观察到足够的疗效,试验才会进入第二阶段。其次最常见的特征是选择剂量或治疗方案。推断无缝设计和操作无缝设计的比例大致相当:讨论:II/III 期无缝设计的主要统计考虑因素包括通过评估和比较不同设计方案的操作特征来优化设计选择,以及显示对总体 I 类错误率的控制。应评估与应计制、药物生产和程序有关的问题,以保持试验的完整性:虽然无缝设计在统计、监管和操作方面有其独特的考虑因素,但它们也非常适合许多开发环境。例如,根据 FDA 的 Optimus 项目解决剂量选择问题,以及解决癌症治疗中越来越多地使用生物标记物和个性化医疗方法的问题。
期刊介绍:
Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health.
The focus areas of the journal are as follows:
Biostatistics
Clinical Trials
Product Development and Innovation
Global Perspectives
Policy
Regulatory Science
Product Safety
Special Populations