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Novel CD19 Fast-CAR-T cells vs. CD19 conventional CAR-T cells for the treatment of relapsed/refractory CD19-positive B-cell acute lymphoblastic leukemia

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收录情况: ◇ 统计源期刊 ◇ CSCD-C ◇ 卓越:领军期刊 ◇ 中华系列

机构: [1]Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing 400037, China. [2]Chongqing Key Laboratory of Hematology and Microenvironment, Chongqing 400037, China. [3]State Key Laboratory of Trauma and Chemical Poisoning, Army Medical University, Chongqing 400037, China. [4]Department of Hematology, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou 550004, China. [5]Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430032, China. [6]Department of Hematology, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi 710032, China. [7]Department of Haematology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, 510260, China. [8]Department of Hematology, The General Hospital of Western Theater Command, PLA, Chengdu, Sichuan 610083, China. [9]Department of Hematology, Henan Cancer Hospital, Zhengzhou, Henan 450008, China. [10]Department of Hematology, 920th Hospital of Joint Logistics Support Force, Kunming, Yunnan 650032, China. [11]Department of Hematology, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200240, China. [12]Department of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230022, China. [13]Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 311100, China.
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关键词: CD19-positive B-cell ALL Relapse/refractory CD19 Fast-CAR-T cells CD19 conventional CAR-T cells Allo-HSCT

摘要:
Treatment with chimeric antigen receptor-T (CAR-T) cells has shown promising effectiveness in patients with relapsed/refractory B-cell acute lymphoblastic leukemia (R/R B-ALL), although the process of preparing for this therapy usually takes a long time. We have recently created CD19 Fast-CAR-T (F-CAR-T) cells, which can be produced within a single day. The objective of this study was to evaluate and contrast the effectiveness and safety of CD19 F-CAR-T cells with those of CD19 conventional CAR-T cells in the management of R/R B-ALL.A multicenter, retrospective analysis of the clinical data of 44 patients with R/R B-ALL was conducted. Overall, 23 patients were administered with innovative CD19 F-CAR-T cells (F-CAR-T group), whereas 21 patients were given CD19 conventional CAR-T cells (C-CAR-T group). We compared the rates of complete remission (CR), minimal residual disease (MRD)-negative CR, leukemia-free survival (LFS), overall survival (OS), and the incidence of cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) between the two groups.Compared with the C-CAR-T group, the F-CAR-T group had significantly higher CR and MRD-negative rates (95.7% and 91.3%, respectively; 71.4% and 66.7%, respectively; P = 0.036 and P = 0.044). No significant differences were observed in the 1-year or 2-year LFS or OS rates between the two groups: the 1-year and 2-year LFS for the F-CAR-T group vs.C-CAR-T group were 47.8% and 43.5% vs. 38.1% and 23.8% (P = 0.384 and P = 0.216), while the 1-year and 2-year OS rates were 65.2% and 56.5% vs. 52.4% and 47.6% (P = 0.395 and P = 0.540). Additionally, among CR patients who underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) following CAR-T-cell therapy, there were no significant differences in the 1-year or 2-year LFS or OS rates: 57.1% and 50.0% vs. 47.8% and 34.8% (P = 0.506 and P = 0.356), 64.3% and 57.1% vs. 65.2% and 56.5% (P = 0.985 and P = 0.883), respectively. The incidence of CRS was greater in the F-CAR-T group (91.3%) than in the C-CAR-T group (66.7%) (P = 0.044). The incidence of ICANS was also greater in the F-CAR-T group (30.4%) than in the C-CAR-T group (9.5%) (P = 0.085), but no treatment-related deaths occurred in the two groups.Compared with C-CAR-T-cell therapy, F-CAR-T-cell therapy has a superior remission rate but also leads to a tolerably increased incidence of CRS/ICANS. Further research is needed to explore the function of allo-HSCT as an intermediary therapy after CAR-T-cell therapy.Copyright © 2025 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license.

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大类 | 2 区 医学
小类 | 2 区 医学:内科
最新[2025]版:
大类 | 2 区 医学
小类 | 2 区 医学:内科
第一作者:
第一作者机构: [1]Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing 400037, China. [2]Chongqing Key Laboratory of Hematology and Microenvironment, Chongqing 400037, China. [3]State Key Laboratory of Trauma and Chemical Poisoning, Army Medical University, Chongqing 400037, China.
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通讯机构: [1]Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing 400037, China. [2]Chongqing Key Laboratory of Hematology and Microenvironment, Chongqing 400037, China. [3]State Key Laboratory of Trauma and Chemical Poisoning, Army Medical University, Chongqing 400037, China.
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