CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Chimeric Antigen Receptor T-cell Therapies in Lymphoma Patients with Central Nervous System Involvement.
Chimeric Antigen Receptor T-cell Therapies in Lymphoma Patients with Central Nervous System Involvement.
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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。
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)。
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.
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