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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Idecabtagene Vicleucel for Relapsed/Refractory Multiple Myeloma: Real-World Experience From the Myeloma CAR T Consortium.
Idecabtagene Vicleucel for Relapsed/Refractory Multiple Myeloma: Real-World Experience From the Myeloma CAR T Consortium.
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在 SOC 背景下,ide-cel 在 RRMM 患者中的安全性和有效性与 II 期关键性 KarMMa 试验相当,尽管大多数患者(75%)不符合试验入组标准。
Idecabtagene vicleucel(ide-cel)是一种自体B细胞成熟抗原靶向的CAR-T 细胞疗法,基于II期关键性KarMMa试验获批用于复发/难治性多发性骨髓瘤(RRMM),该试验显示最佳总缓解率和完全缓解率分别为73%和33%。我们报告了在FDA商业标签下使用标准治疗(SOC)ide-cel的临床结局。
数据回顾性收集自截至2022年2月28日在美国11家机构接受白细胞分离术、意图接受SOC ide-cel治疗的RRMM患者。毒性反应根据美国移植与细胞治疗学会指南进行分级,并按照各机构的政策进行管理。疗效反应根据国际骨髓瘤工作组反应标准进行评定。
在数据截止时,196例接受白细胞采集的患者中有159例接受了ide-cel治疗。120例(75%)输注患者因白细胞采集时的合并症而不符合KarMMa临床试验的入组条件。任何级别和3级细胞因子释放综合征及神经毒性的发生率分别为82%/3%和18%/6%。最佳总体缓解率和完全缓解率分别为84%和42%。在CAR-T 细胞输注后中位随访6.1个月时,中位无进展生存期为8.5个月(95% CI,6.5至未达到),中位总生存期为12.5个月(95% CI,11.3至未达到)。在多变量分析中,既往接受过B细胞成熟抗原靶向治疗、高危细胞遗传学、淋巴细胞清除时东部肿瘤协作组体能状态评分为2以及较年轻的患者无进展生存期较差。
Idecabtagene vicleucel (ide-cel) is an autologous B-cell maturation antigen-directed chimeric antigen receptor T-cell therapy approved for relapsed/refractory multiple myeloma (RRMM) on the basis of the phase II pivotal KarMMa trial, which demonstrated best overall and complete response rates of 73% and 33%, respectively. We report clinical outcomes with standard-of-care (SOC) ide-cel under the commercial Food and Drug Administration label.
Data were retrospectively collected from patients with RRMM who underwent leukapheresis as of February 28, 2022, at 11 US institutions with intent to receive SOC ide-cel. Toxicities were graded per American Society for Transplantation and Cellular Therapy guidelines and managed according to each institution's policies. Responses were graded on the basis of the International Myeloma Working Group response criteria.
One hundred fifty-nine of 196 leukapheresed patients received ide-cel by data cutoff. One hundred twenty (75%) infused patients would have been ineligible for participation in the KarMMa clinical trial because of comorbidities at the time of leukapheresis. Any grade and grade 3 cytokine release syndrome and neurotoxicity occurred in 82/3% and 18/6%, respectively. Best overall and complete response rates were 84% and 42%, respectively. At a median follow-up of 6.1 months from chimeric antigen receptor T infusion, the median progression-free survival was 8.5 months (95% CI, 6.5 to not reached) and the median overall survival was 12.5 months (95% CI, 11.3 to not reached). Patients with previous exposure to B-cell maturation antigen-targeted therapy, high-risk cytogenetics, Eastern Cooperative Oncology Group performance status 2 at lymphodepletion, and younger age had inferior progression-free survival on multivariable analysis.
The safety and efficacy of ide-cel in patients with RRMM in the SOC setting were comparable with those in the phase II pivotal KarMMa trial despite most patients (75%) not meeting trial eligibility criteria.
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