医学
内科学
多发性骨髓瘤
细胞因子释放综合征
耐火材料(行星科学)
嵌合抗原受体
CD38
肿瘤科
胃肠病学
免疫学
免疫疗法
干细胞
川地34
癌症
物理
天体生物学
生物
遗传学
作者
Huan Zhang,Man Liu,Xia Xiao,Hairong Lv,Yanyu Jiang,Xin Li,Yuan Tan,Mingfeng Zhao
标识
DOI:10.1080/10428194.2022.2030476
摘要
Chimeric antigen receptor T (CAR-T) cells are a promising approach in hematopoietic malignancies. We evaluated the safety and efficacy of a combination of humanized anti-BCMA and murine anti-CD38 CAR-T cell therapy in patients with relapsed or refractory multiple myeloma (R/RMM). Twenty-two R/RMM patients, with a median age of 56 years and a median number of previous therapies of 8, were included in the study. Both CAR-T cells infusion doses were 2.0 × 106/kg. The overall response rate (ORR) was 90.9%, with 12 patients (54.5%) achieving a strict complete response/complete response (sCR/CR). The 24-month overall survival (OS) rate was 56.6%, and the progression-free survival (PFS) rate was 48.7%. Cytokine release syndrome (CRS) of grades 1-2 occurred in 16 patients (72.7%) and of grade ≥3 in six patients (27.3%). Immune effector cell-associated neurotoxic syndrome (ICANS) of grades 1-2 occurred in three patients (13.6%). The combination therapy is potential in R/RMM patients.Trial registration: The patients were enrolled in clinical trials registered as ChiCTR1800017051.
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