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.
引用
收藏
页码:1275 / +
页数:17
相关论文
共 13 条
  • [11] Efficacy and safety results from a phase 1b/2, multicenter, open-label study of oprozomib and dexamethasone in patients with relapsed and/or refractory multiple myeloma
    Hari, Parameswaran
    Paba-Prada, Claudia E.
    Voorhees, Peter M.
    Frye, John
    Chang, Yu-Lin
    Moreau, Philippe
    Zonder, Jeffrey
    Boccia, Ralph
    Shain, Kenneth H.
    LEUKEMIA RESEARCH, 2019, 83
  • [12] Effectiveness and safety of anti-BCMA chimeric antigen receptor T-cell treatment in relapsed/refractory multiple myeloma: a comprehensive review and meta-analysis of prospective clinical trials
    Hu, Dingyuan
    Chen, Liming
    Yan, Diqin
    Dong, Wenliang
    Chen, Min
    Niu, Suping
    Wang, Simin
    Zhang, Jiaojiao
    Nie, Xiaoyan
    Fang, Yi
    FRONTIERS IN PHARMACOLOGY, 2023, 14
  • [13] CD19 chimeric antigen receptor-T cells as bridging therapy to allogeneic hematopoietic cell transplantation improves outcome in patients with refractory/relapsed B-cell acute lymphoblastic leukemia
    Liu, Jie
    Xu, Mengyuan
    Zhang, Xiaoqian
    Zhang, Zhuo
    Zhong, Tao
    Yu, Hongjuan
    Fu, Yueyue
    Meng, Hongbin
    Feng, Jiawei
    Zou, Xindi
    Han, Xueying
    Kang, Liqing
    Yu, Lei
    Li, Limin
    HELIYON, 2024, 10 (13)