嵌合抗原受体
Blinatumoab公司
医学
汽车T细胞治疗
细胞疗法
细胞因子释放综合征
免疫学
人口
肿瘤科
耐火材料(行星科学)
CD19
免疫疗法
内科学
重症监护医学
干细胞
抗原
生物
免疫系统
遗传学
天体生物学
环境卫生
作者
Claire Roddie,Alexandros Rampotas
出处
期刊:Blood
[American Society of Hematology]
日期:2024-09-24
标识
DOI:10.1182/blood.2023022922
摘要
Chimeric Antigen Receptor T-cell therapy (CAR-T) targeting CD19 has transformed the management of relapsed/refractory (r/r) B-Acute Lymphoblastic Leukemia (B-ALL), with FDA approval of tisagenlecleucel (tisa-cel) for pediatric/young adult patients and brexucabtagene autoleucel (brexu-cel) for adults. Efficacy is contingent upon several factors including disease burden. Emerging data suggests that bridging therapy, lymphodepletion and for some patients, consolidation therapy have an important role in the success of treatment. Further, strategies to define and manage immunotoxic side effects including hematotoxicity is critical to safe delivery. Advancements in CAR-T design beyond CD19 represent an ongoing therapeutic evolution. Overall, CAR-T therapy signifies a paradigm shift in B-ALL management, with the potential for improved remission and survival in a historically challenging patient population.
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