Park Jae H, Rivière Isabelle, Gonen Mithat, Wang Xiuyan, Sénéchal Brigitte, Curran Kevin J, Sauter Craig, Wang Yongzeng, Santomasso Bianca, Mead Elena, Roshal Mikhail, Maslak Peter, Davila Marco, Brentjens Renier J, Sadelain Michel
From the Leukemia Service, Department of Medicine (J.H.P., C.S., P.M., R.J.B.), the Michael G. Harris Cell Therapy and Cell Engineering Facility (I.R., X.W., B. Sénéchal, Y.W.), the Center for Cell Engineering (J.H.P., I.R., X.W., R.J.B., M.S.), and the Departments of Epidemiology and Biostatistics (M.G.), Pediatrics (K.J.C.), Neurology (B. Santomasso), Anesthesiology and Critical Care Medicine (E.M.), and Pathology (M.R.), Memorial Sloan Kettering Cancer Center, and the Department of Medicine, Joan and Sanford Weill Medical College of Cornell University (J.H.P., C.S., R.J.B.) - all in New York; and the Department of Blood and Marrow Transplant and Cellular Immunotherapy, H. Lee Moffitt Cancer Center, Tampa, FL (M.D.).
N Engl J Med. 2018 Feb 1;378(5):449-459. doi: 10.1056/NEJMoa1709919.
CD19-specific chimeric antigen receptor (CAR) T cells induce high rates of initial response among patients with relapsed B-cell acute lymphoblastic leukemia (ALL) and long-term remissions in a subgroup of patients.
We conducted a phase 1 trial involving adults with relapsed B-cell ALL who received an infusion of autologous T cells expressing the 19-28z CAR at the Memorial Sloan Kettering Cancer Center (MSKCC). Safety and long-term outcomes were assessed, as were their associations with demographic, clinical, and disease characteristics.
A total of 53 adults received 19-28z CAR T cells that were manufactured at MSKCC. After infusion, severe cytokine release syndrome occurred in 14 of 53 patients (26%; 95% confidence interval [CI], 15 to 40); 1 patient died. Complete remission was observed in 83% of the patients. At a median follow-up of 29 months (range, 1 to 65), the median event-free survival was 6.1 months (95% CI, 5.0 to 11.5), and the median overall survival was 12.9 months (95% CI, 8.7 to 23.4). Patients with a low disease burden (<5% bone marrow blasts) before treatment had markedly enhanced remission duration and survival, with a median event-free survival of 10.6 months (95% CI, 5.9 to not reached) and a median overall survival of 20.1 months (95% CI, 8.7 to not reached). Patients with a higher burden of disease (≥5% bone marrow blasts or extramedullary disease) had a greater incidence of the cytokine release syndrome and neurotoxic events and shorter long-term survival than did patients with a low disease burden.
In the entire cohort, the median overall survival was 12.9 months. Among patients with a low disease burden, the median overall survival was 20.1 months and was accompanied by a markedly lower incidence of the cytokine release syndrome and neurotoxic events after 19-28z CAR T-cell infusion than was observed among patients with a higher disease burden. (Funded by the Commonwealth Foundation for Cancer Research and others; ClinicalTrials.gov number, NCT01044069 .).
CD19特异性嵌合抗原受体(CAR)T细胞在复发的B细胞急性淋巴细胞白血病(ALL)患者中诱导出较高的初始缓解率,并使部分患者获得长期缓解。
我们在纪念斯隆凯特琳癌症中心(MSKCC)开展了一项1期试验,纳入复发B细胞ALL的成人患者,给予其输注表达19-28z CAR的自体T细胞。评估了安全性和长期结局,以及它们与人口统计学、临床和疾病特征的相关性。
共有53名成人接受了在MSKCC制备的19-28z CAR T细胞。输注后,53例患者中有14例(26%;95%置信区间[CI],15%至40%)发生严重细胞因子释放综合征;1例患者死亡。83%的患者观察到完全缓解。在中位随访29个月(范围1至65个月)时,中位无事件生存期为6.1个月(95%CI,5.0至11.5个月),中位总生存期为12.9个月(95%CI,8.7至23.4个月)。治疗前疾病负担较低(骨髓原始细胞<5%)的患者缓解持续时间和生存期显著延长,中位无事件生存期为10.6个月(95%CI,5.9至未达到),中位总生存期为20.1个月(95%CI,8.7至未达到)。疾病负担较高(骨髓原始细胞≥5%或髓外疾病)的患者与疾病负担较低的患者相比,细胞因子释放综合征和神经毒性事件的发生率更高,长期生存期更短。
在整个队列中,中位总生存期为12.9个月。在疾病负担较低的患者中,中位总生存期为20.1个月,并且与疾病负担较高的患者相比,在输注19-28z CAR T细胞后细胞因子释放综合征和神经毒性事件的发生率显著更低。(由英联邦癌症研究基金会及其他机构资助;ClinicalTrials.gov编号,NCT01044069。)