A national service for delivering CD19 CAR‐Tin large B‐cell lymphoma – The UK real‐world experience

医学 细胞因子释放综合征 汽车T细胞治疗 人口 淋巴瘤 内科学 耐火材料(行星科学) 临床试验 肿瘤科 嵌合抗原受体 癌症 免疫疗法 天体生物学 环境卫生 物理
作者
Andrea Kühnl,Claire Roddie,Amy A. Kirkwood,Eleni Tholouli,Tobias Menne,Amit K. Patel,Caroline Besley,Sridhar Chaganti,Robin Sanderson,Maeve O’Reilly,Jane E. Norman,Wendy Osborne,Adrian Bloor,Sanne Lugthart,Ram Malladi,Piers Patten,Lorna Neill,Núria Martínez‐Cibrián,Hannah Kennedy,Elizabeth H. Phillips
出处
期刊:British Journal of Haematology [Wiley]
卷期号:198 (3): 492-502 被引量:112
标识
DOI:10.1111/bjh.18209
摘要

CD19 CAR-T have emerged as a new standard treatment for relapsed/refractory (r/r) large B-cell lymphoma (LBCL). CAR-T real-world (RW) outcomes published to date suggest significant variability across countries. We provide results of a large national cohort of patients intended to be treated with CAR-T in the UK. Consecutive patients with r/r LBCL approved for CAR-T by the National CAR-T Clinical Panel between December 2018 and November 2020 across all UK CAR-T centres were included. 404/432 patients were approved [292 axicabtagene ciloleucel (axi-cel), 112 tisagenlecleucel (tisa-cel)], 300 (74%) received the cells. 110/300 (38.3%) patients achieved complete remission (CR) at 6 months (m). The overall response rate was 77% (52% CR) for axi-cel, 57% (44% CR) for tisa-cel. The 12-month progression-free survival was 41.8% (axi-cel) and 27.4% (tisa-cel). Median overall survival for the intention-to-treat population was 10.5 m, 16.2 m for infused patients. The incidence of grade ≥3 cytokine release syndrome and neurotoxicity were 7.6%/19.6% for axi-cel and 7.9%/3.9% for tisa-cel. This prospective RW population of CAR-T eligible patients offers important insights into the clinical benefit of CD19 CAR-T in LBCL in daily practice. Our results confirm long-term efficacy in patients receiving treatment similar to the pivotal trials, but highlight the significance of early CAR-T failure.
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