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:A national service for delivering CD19 CAR-Tin large B-cell lymphoma - The UK real-world experience.
A national service for delivering CD19 CAR-Tin large B-cell lymphoma - The UK real-world experience.
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CD19 CAR-T 已成为复发/难治性(r/r)大 B 细胞淋巴瘤(LBCL)的新标准治疗。迄今为止发表的 CAR-T 真实世界(RW)结局提示各国之间存在显著差异。
我们提供了英国一个大型全国性队列中计划接受 CAR-T 治疗的患者结果。纳入 2018 年 12 月至 2020 年 11 月期间由国家 CAR-T 临床专家组批准接受 CAR-T 治疗的所有英国 CAR-T 中心的连续 r/r LBCL 患者。404/432 例患者获得批准[292 例 axicabtagene ciloleucel(axi-cel),112 例 tisagenlecleucel(tisa-cel)],300 例(74%)接受了细胞输注。110/300(38.3%)例患者在 6 个月(m)时达到完全缓解(CR)。axi-cel 的总体缓解率为 77%(52% CR),tisa-cel 为 57%(44% CR)。12 个月无进展生存率分别为 41.8%(axi-cel)和 27.4%(tisa-cel)。意向治疗人群的中位总生存期为 10.5 m,输注患者为 16.2 m。3 级细胞因子释放综合征和神经毒性的发生率分别为 axi-cel 7.6%/19.6% 和 tisa-cel 7.9%/3.9%。这一前瞻性 RW 人群中符合 CAR-T 条件的患者为 CD19 CAR-T 在 LBCL 日常实践中的临床获益提供了重要见解。
我们的结果证实了接受与关键试验相似治疗的患者具有长期疗效,但突出了早期 CAR-T 失败的重要性。
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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