Suppr超能文献

关于布雷西尤单抗自体细胞疗法治疗复发或难治性B细胞急性淋巴细胞白血病患者的临床见解

Clinical Insights on Brexucabtagene Autoleucel for the Treatment of Patients with Relapsed or Refractory B-Cell Acute Lymphoblastic Leukemia.

作者信息

Kopmar Noam E, Cassaday Ryan D

机构信息

Division of Hematology and Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.

Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

出版信息

Cancer Manag Res. 2024 Nov 14;16:1587-1596. doi: 10.2147/CMAR.S379807. eCollection 2024.

Abstract

Autologous chimeric antigen receptor-modified T-cell therapy (CAR-T) has revolutionized treatment paradigms across multiple lymphoid malignancies, including relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL). The introduction of the CD19-directed CAR-T product brexucabtagene autoleucel (brexu-cel; Tecartus) in October 2021 made this treatment approach available for the first time for adults with R/R B-ALL, a historically challenging clinical entity to treat. In this review, we will discuss the pivotal clinical trial data from the ZUMA-3 study that led to the US Food and Drug Administration (FDA) approval of brexu-cel, including clinical outcomes and key toxicity data (most importantly, the incidence and severity of cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome). Additionally, we will compare and contrast these data from the ZUMA-3 study with "real-world" data from examinations of patient outcomes with brexu-cel as an FDA-approved therapy in R/R B-ALL, and discuss practical considerations with brexu-cel use in the clinic, including the role of consolidative allografting for patients post-brexu-cel. We finish by discussing future directions for CAR-T use in R/R B-ALL with the anticipated introduction of a new CD19-directed CAR-T product - obecabtagene autoleucel - in the near future.

摘要

自体嵌合抗原受体修饰的T细胞疗法(CAR-T)彻底改变了多种淋巴系统恶性肿瘤的治疗模式,包括复发/难治性(R/R)B细胞急性淋巴细胞白血病(B-ALL)。2021年10月,靶向CD19的CAR-T产品brexucabtagene autoleucel(brexu-cel;Tecartus)的推出,使这种治疗方法首次可用于患有R/R B-ALL的成人患者,这是一个历来治疗颇具挑战性的临床实体。在本综述中,我们将讨论来自ZUMA-3研究的关键临床试验数据,这些数据促使美国食品药品监督管理局(FDA)批准了brexu-cel,包括临床结果和关键毒性数据(最重要的是,细胞因子释放综合征和免疫效应细胞相关神经毒性综合征的发生率和严重程度)。此外,我们将把ZUMA-3研究中的这些数据与来自对brexu-cel作为FDA批准的R/R B-ALL治疗方法的患者结局检查的“真实世界”数据进行比较和对比,并讨论在临床中使用brexu-cel的实际考虑因素,包括巩固性同种异体移植对brexu-cel治疗后患者的作用。我们将通过讨论在不久的将来预期引入一种新的靶向CD19的CAR-T产品——奥贝卡他基因自体细胞(obecabtagene autoleucel)后,CAR-T在R/R B-ALL中的未来应用方向来结束本文。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d355/11571986/0a8fede9466e/CMAR-16-1587-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验