细胞因子释放综合征与 T 细胞参与性双特异性抗体的临床药理学:当前见解与药物开发策略》。

IF 10 1区 医学 Q1 ONCOLOGY
Kendra K Radtke, Brendan C Bender, Zao Li, David C Turner, Sumedha Roy, Anton Belousov, Chi-Chung Li
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引用次数: 0

摘要

细胞因子释放综合征(CRS)是 T 细胞疗法(包括 T 细胞结合双特异性抗体(T-BiSp))中常见的急性毒性反应。有效的 CRS 管理和预防对于 T-BiSp 的开发至关重要。在已获批的 9 种 T-BiSp 中,有 7 种需要住院治疗,严重病例需要临床干预,这凸显了缓解策略对减轻医疗负担和改善患者预后的重要性。在本综述中,我们将讨论有关 CRS 缓解、管理和预测的新证据。我们将介绍不同的剂量优化策略、当前和新兴的(预)治疗策略、药物开发过程中使用的定量药理学工具以及生物标志物和预测因素。通过审查 T-BiSp 许可申请以及会议和出版物中新出现的数据,我们将深入了解加大剂量和制剂对 CRS 的影响,以及 CRS 与细胞因子动态和药物水平的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Pharmacology of Cytokine Release Syndrome with T-cell Engaging Bispecific Antibodies: Current Insights and Drug Development Strategies.

Cytokine release syndrome (CRS) is a common acute toxicity in T-cell therapies, including T-cell engaging bispecific antibodies (T-BiSp). Effective CRS management and prevention is crucial in T-BiSp development. Required hospitalization for 7 of the 9 approved T-BiSp and the need for clinical intervention in severe cases highlight the importance of mitigation strategies to reduce healthcare burden and improve patient outcome. In this review, we discuss the emerging evidence on CRS mitigation, management, and prediction. We cover different strategies for dose optimization, current and emerging (pre)treatment strategies, quantitative pharmacology tools employed during drug development, and biomarkers and predictive factors. Insights are gleaned on step-up dosing and formulation effects on CRS and CRS relationships with cytokine dynamics and drug levels gathered through review of T-BiSp licensing applications and emerging data from conferences and publications.

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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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