← 返回

中枢神经系统受累的淋巴瘤患者的 CAR-T 细胞治疗

英文原题:Chimeric Antigen Receptor T-cell Therapies in Lymphoma Patients with Central Nervous System Involvement.

查看英文原题

Chimeric Antigen Receptor T-cell Therapies in Lymphoma Patients with Central Nervous System Involvement.

PubMed 2022/12/15(内容时间) Hematol Oncol Stem Cell Ther

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

基于我们对 PubMed 文献的回顾,我们得出结论,CAR-T 细胞疗法可能对 CNS 淋巴瘤患者有益,具有前景良好的缓解率和可接受的 AE。然而,在获得更大样本量的数据之前,无法得出明确结论。

研究思路结论见上方概要

CAR-T 细胞疗法显著改善了复发/难治性(R/R)B细胞非霍奇金淋巴瘤(B-NHL)患者的结局。然而,由于疗效和安全性不确定,大多数临床试验排除了中枢神经系统(CNS)受累的患者。

2022年1月1日,我们检索了PubMed,以识别所有与当前商业CAR-T 细胞疗法治疗B-NHL相关的已发表文献,包括tisagenlecleucel(tisa-cel)、axicabtagene ciloleucel(axi-cel)、brexucabtagene autoleucel(brexu-cel)和lisocabtagene maraleucel(liso-cel)。纳入并总结了涉及原发性或继发性CNS淋巴瘤患者,并评估了缓解率、不良事件(AEs)或生存期的研究。

在此,我们总结了11项符合纳入标准的研究结果,报告了58例伴有CNS受累的淋巴瘤患者,其中44例可评估临床反应,25例可评估免疫效应细胞相关神经毒性综合征(ICANS),48例可评估细胞因子释放综合征(CRS)。62%(16/26)的患者达到客观缓解,52%(23/44)的患者达到CR。44%(11/25)发生ICANS,35%(17/48)发生重度ICANS(3级)。63%(15/24)的患者报告CRS,而7%(3/42)的患者报告重度CRS(3级)。

展开英文摘要原文

CAR T-cell therapy has significantly improved the outcomes of patients with relapsed or refractory (R/R) B-cell non-Hodgkin lymphoma (B-NHL). However, most clinical trials excluded patients with central nervous system (CNS) involvement due to uncertain efficacy and safety. MATERIAL AND METHODS: On January 1, 2022, we searched PubMed to identify all published literature associated with current commercial CAR T-cell therapies for B-NHL, including tisagenlecleucel (tisa-cel), axicabtagene ciloleucel (axi-cel), brexucabtagene autoleucel (brexu-cel), and lisocabtagene maraleucel (liso-cel). Studies that involved patients with either primary or secondary CNS lymphoma, and evaluated response rate, adverse events (AEs), or survival were included and summarized. RESULT: Herein, we summarize the results of 11 studies qualified for our inclusion criteria, reporting 58 lymphoma patients with CNS Involvement with 44 evaluable for clinical response, 25 for immune effector cell-associated neurotoxicity syndrome (ICANS) and 48 for Cytokine release syndrome (CRS). Objective response was achieved in 62% (16/26) of patients, and CR was achieved in 52% (23/44) of patients. Forty-four percent (11/25) developed ICANS, and 35% (17/48) developed severe ICANS (grade 3). CRS was reported in 63% (15/24) of patients, while severe CRS (grade 3) was reported in 7% (3/42) of patients.

Based on our PubMed literature review, we conclude that CAR T-cell therapy may benefit patients with CNS lymphoma with promising response rates and acceptable AE. However, definite conclusions cannot be drawn until data with a larger sample size is available.

论文信息

作者
Yi D、Gergis M、Elgohary G、Hsu J、Yang Y、Bi X、Gergis U
单位
Thomas Jefferson University Sidney Kimmel Medical College, United States.United States
文献类型
综述
期刊
Hematology/oncology and stem cell therapy2022 Dec 15
原文标识
PubMed 36537908 · DOI 10.56875/2589-0646.1024