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:Real-life experiences with CAR T-cell therapy with idecabtagene vicleucel (ide-cel) for triple-class exposed relapsed/refractory multiple myeloma patients.
Real-life experiences with CAR T-cell therapy with idecabtagene vicleucel (ide-cel) for triple-class exposed relapsed/refractory multiple myeloma patients.
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我们报告了首批接受商业化 ide-cel 治疗的复发/难治性多发性骨髓瘤队列之一。
CAR-T 改变了复发/难治性多发性骨髓瘤(RRMM)治疗格局,带来前所未有缓解。伊德卡布塔基因-维克鲁赛(ide-cel)近期获批用于三类药物暴露后的RRMM。本文报告商业化ide-cel真实世界应用经验。
单一学术中心回顾首批16例三类药物暴露RRMM患者,评估毒性、疗效、CAR-T 扩增和可溶性BCMA(sBCMA)。
2022年6至10月连续治疗16例,中位年龄69岁;38%高危细胞遗传学,19%为R-ISS III期,31%髓外病变;既往治疗中位6线。制备成功率88%,6%需再次单采,6%接受超规格产品。3个月总体缓解率69%(严格完全缓解44%、完全缓解6%、非常好部分缓解19%)。15例(94%)发生CRS,88%为1级、6%为2级;1例(6%)发生1级ICANS;发热性中性粒细胞减少69%,感染31%;持续血液学毒性25%。其他毒性包括肝酶升高38%、结肠炎6%(3级)和DIC 6%(2级)。CAR-T 扩增较高者应答更多(100%比38%);无应答者常见sBCMA未下降或趋于平台。
该首批商业ide-cel队列ORR为69%,安全性可管理,但持续血液学毒性仍是重要挑战。疗效与体内CAR-T 扩增相关,需进一步研究优化扩增。
Chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment landscape of relapsed/refractory multiple myeloma (RRMM), leading to unprecedented responses in this patient population. Idecabtagene vicleucel (ide-cel) has been recently approved for treatment of triple-class exposed RRMM. We report real-life experiences with the commercial use of ide-cel in RRMM patients.
We performed a retrospective analysis of the first 16 triple-class exposed RRMM patients treated with ide-cel at a single academic center. We assessed toxicities, response to treatment, CAR T expansion and soluble BCMA (sBCMA) levels.
We identified 16 consecutive RRMM patients treated with ide-cel between 06-10/2022. Median age was 69 years, 6 (38%) patients had high-risk cytogenetics, 3 (19%) R-ISS stage III, and 5 (31%) extramedullary disease. Median number of previous treatment lines was 6 (3-12). Manufacturing success rate was 88% (6% required second lymphapheresis, 6% received an out-of-specification product). At 3 months, the overall response rate (ORR) was 69% (44% sCR, 6% CR, 19% VGPR). Cytokine release syndrome (CRS) occurred in 15 (94%) patients (88% G1, 6% G2), immune effector-cell associated neurotoxicity syndrome (ICANS) in 1 (6% G1), febrile neutropenia in 11 (69%), and infections in 5 (31%). Prolonged hematologic toxicity occurred in 4/16 (25%) patients. Other non-hematological toxicities were elevated hepatic enzymes (38%), colitis (6%, G3) and DIC (6%, G2). Responses were more frequent in patients with higher CAR T expansion (100% vs 38%), and lack of decrease or plateau of sBCMA levels was typically observed in non-responders.
We report one of the first cohorts of RRMM treated with commercial ide-cel. The ORR was 69% and safety profile was manageable, but prolonged hematologic toxicity still represents a major challenge. Responses correlated with in vivo CAR T cell expansion, underlining the need of further research to optimize CAR T expansion.
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