评估药物组合的细胞治疗癌症临床试验的剂量发现设计。

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Evan M. Bagley , Nolan A. Wages
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引用次数: 0

摘要

细胞疗法已经成为治疗多种癌症的一种有希望的方式。尽管如此,它们作为单一疗法的疗效有限,这促使人们对它们作为药物组合的一部分可能发挥的作用产生了兴趣。本文介绍了一种用于评估药物组合的I期癌症试验的新型剂量发现设计,其中一种药物是细胞疗法。我们的设计采用了偏序连续重新评估方法(POCRM)来考虑迟发性剂量限制性毒性(DLT)和由于制造细胞治疗产品的复杂性而引起的可行性问题。我们在一项拟议的试验中说明了我们的设计,以评估基于利妥昔单抗的双特异性抗体活化T细胞产品和纳武单抗联合治疗高级别b细胞淋巴瘤。我们还提供了模拟结果,证明我们的设计能够准确识别可行的最大耐受剂量组合(FMTDC),同时管理迟发性dlt和可行性问题。我们的方法旨在改善细胞治疗癌症临床试验的I期药物组合景观。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dose-finding designs for cell therapy cancer clinical trials evaluating drug-combinations
Cell therapies have taken hold as a promising modality of treatment for multiple types of cancer. Despite this, their efficacy as a monotherapy has been limited, driving interest in their possible role as part of a drug combination. This paper introduces a novel dose-finding design for phase I cancer trials assessing drug combinations where one of the drugs is a cell therapy. Our design adapts the partial order continual reassessment method (POCRM) to account for late-onset dose-limiting toxicities (DLT) and feasibility concerns due to complexities related to manufacturing the cell therapy product. We illustrate our design on a proposed trial to assess the combination of a Rituximab-based bispecific antibody activated T cell product and Nivolumab for the treatment of high-grade B-cell lymphoma. We also provide simulation results that demonstrate our design's ability to accurately identify the feasible maximum tolerated dose combination (FMTDC) while managing late-onset DLTs and feasibility concerns. Our methodology aims to improve the phase I drug combination landscape for cell therapy cancer clinical trials.
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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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