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关于美国食品药品监督管理局(FDA)批准曲拉西利(Cosela)用于广泛期小细胞肺癌的情况。

Concerning FDA approval of trilaciclib (Cosela) in extensive-stage small-cell lung cancer.

作者信息

Powell Kerrington, Prasad V

机构信息

College of Medicine, Texas A&M Health Science Center, College Station, TX 77843, United States.

Department of Epidemiology and Biostatistics, University of California San Francisco, 550 16th St, 2nd Fl, San Francisco, CA 94158, United States.

出版信息

Transl Oncol. 2021 Nov;14(11):101206. doi: 10.1016/j.tranon.2021.101206. Epub 2021 Aug 19.

Abstract

Trilaciclib is a recently approved cyclin-dependent kinase 4/6 inhibitor that is designed to decrease the incidence of chemotherapy-induced myelosuppression in adult patients with extensive-stage small-cell lung cancer receiving chemotherapy. Currently, this first-in-class therapy raises two open issues: its bio-plausibility and paucity of evidence demonstrating a lasting impact on clinical endpoints. Based on the existing phase 2 data, trilaciclib appears to be a therapy that can make a positive impact by preventing myelosuppression, but empirical validation with larger phase III trials should be conducted to confirm these benefits. The purpose of this article is to facilitate discussion about the role of trilaciclib in clinical practice and the need for additional trials.

摘要

曲拉西利是一种最近获批的细胞周期蛋白依赖性激酶4/6抑制剂,旨在降低接受化疗的广泛期小细胞肺癌成年患者化疗诱导的骨髓抑制发生率。目前,这种同类首创疗法存在两个尚未解决的问题:其生物学合理性以及缺乏证据证明对临床终点有持久影响。基于现有的2期数据,曲拉西利似乎是一种可通过预防骨髓抑制产生积极影响的疗法,但应通过更大规模的3期试验进行实证验证以确认这些益处。本文旨在促进关于曲拉西利在临床实践中的作用以及开展更多试验的必要性的讨论。

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