Phase II, Open-Label Study of Ciltacabtagene Autoleucel, an Anti-B-Cell Maturation Antigen Chimeric Antigen Receptor-T-Cell Therapy, in Chinese Patients With Relapsed/Refractory Multiple Myeloma (CARTIFAN-1)

被引:35
|
作者
Mi, Jian-Qing [1 ]
Zhao, Wanhong [2 ]
Jing, Hongmei [3 ]
Fu, Weijun [4 ]
Hu, Jianda [5 ]
Chen, Lijuan [6 ]
Zhang, Yiwen [7 ]
Yao, Dan [8 ]
Chen, Diana [8 ]
Schecter, Jordan M. [9 ]
Yang, Fan [8 ]
Tian, Xiaochen [8 ]
Sun, Huabin [9 ]
Zhuang, Sen Hong [8 ]
Ren, Jimmy [8 ]
Fan, Xiaohu [7 ]
Jin, Jie [10 ]
Niu, Ting [11 ]
Chen, Sai-Juan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Hematol, Natl Res Ctr Translat Med Shanghai,Sch Med,State K, Shanghai, Peoples R China
[2] Xi An Jiao Tong Univ, Affiliated Hosp 2, Xian, Shaanxi, Peoples R China
[3] Peking Univ Third Hosp, Beijing, Peoples R China
[4] Tongji Univ, Shanghai Changzheng Hosp, Shanghai Peoples Hosp 4, Sch Med, Shanghai, Peoples R China
[5] Fujian Med Univ Union Hosp, Fuzhou, Fujian, Peoples R China
[6] Jiangsu Prov Hosp, Nanjing, Jiangsu, Peoples R China
[7] Legend Biotech China, Nanjing, Jiangsu, Peoples R China
[8] Janssen China Res & Dev, Shanghai, Peoples R China
[9] Janssen Res & Dev, Raritan, NJ USA
[10] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Hangzhou, Zhejiang, Peoples R China
[11] Sichuan Univ, West China Hosp, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
MINIMAL RESIDUAL DISEASE; DEXAMETHASONE; DARATUMUMAB;
D O I
10.1200/JCO.22.00690
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE CARTIFAN-1 aimed to evaluate the efficacy and safety of ciltacabtagene autoleucel (ciltacel), a B-cell maturation antigen-targeting chimeric antigen receptor T-cell therapy, in Chinese patients with relapsed/ refractory multiple myeloma (RRMM).METHODS This pivotal phase II, open-label study (ClinicalTrials.gov identifier: NCT03758417), conducted across eight sites in China, enrolled adult patients with RRMM who had received >_ 3 lines of prior therapy, including a proteasome inhibitor and immunomodulatory drug. Patients received a single infusion of ciltacel (target dose 0.75 X 10(6) chimeric antigen receptor-positive viable T cells/kg). The primary end point was overall response rate. Secondary end points included progression-free survival (PFS), overall survival (OS), and incidence and severity of adverse events (AEs).RESULTS As of the clinical cutoff of July 19, 2021, 48 patients received a ciltacel infusion. At an 18-month median follow-up, the overall response rate was 89.6% (95% CI, 77.3 to 96.5), with a median time to first response of approximately 1 month; 77.1% of patients (95% CI, 62.7 to 88.0) achieved complete response or better. Medians for duration of response, PFS, and OS were not reached. The 18-month PFS and OS rates were 66.8% (95% CI, 49.4 to 79.4) and 78.7% (95% CI, 64.0 to 88.0), respectively. Hematologic AEs were common, including anemia (1 00%), neutropenia (97 .9%), lymphopenia (95.8%), and thrombocytopenia (87.5%). Cytokine release syndrome occurred in 97.9% of patients (35.4% grade 3/4); the median time to onset was 7 days, and the median duration was 5 days. Infections occurred in 85.4% of patients (37.5% grade 3/4). Ten deaths occurred after cilta-cel infusion, eight of which were due to treatment-related AEs.CONCLUSION These data demonstrate a favorable risk-benefit profile for a single infusion of ciltacel, resulting in early, deep, and durable responses in heavily pretreated patients with RRMM in China.
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收藏
页码:1275 / +
页数:17
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