改进的组合i3 + 3设计用于肿瘤学中新颖的联合剂量发现试验。

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Jiaxin Liu , Shijie Yuan , Qiqi Deng , Yuan Ji
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引用次数: 0

摘要

我们考虑了一种改良的Ci3 + 3 (mcci3 + 3)设计,用于双药剂量发现试验,其中两种药物都在多个剂量下进行测试。这通常发生在药物是新疗法的时候。mc3 + 3设计根据实际需要提供两级或三级版本。第一阶段以单药剂量递增开始,第二阶段开展两种药物的无模型联合剂量发现,第三阶段可选地采用基于模型的设计。MCi3 + 3旨在维持一个相对简单的框架,以促进实际应用,同时也解决新-新组合剂量发现所特有的挑战。通过仿真,我们证明了MCi3 + 3设计能够熟练地管理各种毒性场景。它具有与其他组合设计相同的操作特性,同时提供更高的安全性。这一设计是为现实生活中的临床试验而设计和测试的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The modified combo i3 + 3 design for novel-novel combination dose-finding trials in oncology
We consider a modified Ci3 + 3 (MCi3 + 3) design for dual-agent dose-finding trials in which both agents are tested on multiple doses. This usually happens when the agents are novel therapies. The MCi3 + 3 design offers a two-stage or three-stage version, depending on the practical need. The first stage begins with single-agent dose escalation, the second stage launches a model-free combination dose finding for both agents, and optionally, the third stage follows with a model-based design. MCi3 + 3 aims to maintain a relatively simple framework to facilitate practical application, while also address challenges that are unique to novel-novel combination dose finding. Through simulations, we demonstrate that the MCi3 + 3 design adeptly manages various toxicity scenarios. It exhibits operational characteristics on par with other combination designs, while offering an enhanced safety profile. The design is motivated and tested for a real-life clinical trial.
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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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