Xiao Jinyan, Liu Yujie, Shen Yifan, Li Jiaqi, Wang Ying, Chen Suning, Tang Xiaowen, Yang Lin, Zhou Biqi, Xu Yang, Wu Depei
Jiangsu Institute of Hematology, National Clinical Research Center for Hematologic Diseases, The First Affiliated Hospital of Soochow University, Suzhou, China.
Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, China.
Hematol Oncol. 2025 May;43(3):e70081. doi: 10.1002/hon.70081.
Relapse and refractory T-cell acute lymphoblastic leukemia and lymphoblastic lymphoma (R/R T-ALL/LBL) patients have poor outcomes. Chimeric antigen receptor (CAR)-T-cell therapy for T-ALL/LBL has shown encouraging results in the early stages of clinical trials. Here, we retrospectively analyzed the outcomes of 12 patients with R/R T-ALL/LBL who received CD7 CAR-T cell therapy. Eleven patients received autologous CAR-T cells, while one patient received allogeneic CAR-T cells. On Day 28 post-infusion, 67% (8/12) of patients achieved an overall response (ORR). At a median follow-up of 134 (14-925) days, the median overall survival (OS) was 134 days, and the progression-free survival (PFS) was 81 days. Among the 8 patients who achieved remission after CD7 CAR-T cell infusion, 5 patients received consolidation allogeneic hematopoietic stem cell transplantation (allo-HSCT). Compared with 3 patients who did not undergo consolidation allo-HSCT, patients with allo-HSCT as consolidation showed a trend toward better OS (allo-HSCT vs. control: 6-month OS, 60% vs. 33.3%, p = 0.073) and better PFS (allo-HSCT vs. control: 6-month PFS, 60% vs. 0%, p = 0.022). Cytokine release syndrome (CRS) occurred in all patients (grade 1-2 in 67% of patients, grade 3 in 33% of patients), and one patient experienced neurotoxicity. CD7 CAR-T cell therapy is a promising option for R/R T-ALL/LBL patients with manageable adverse events. Moreover, CD7 CAR-T cell infusion followed by consolidation allo-HSCT in R/R T-ALL/LBL patients might play an important role in prolonging remission duration.
复发难治性T细胞急性淋巴细胞白血病和淋巴细胞淋巴瘤(R/R T-ALL/LBL)患者的预后较差。嵌合抗原受体(CAR)T细胞疗法治疗T-ALL/LBL在临床试验早期已显示出令人鼓舞的结果。在此,我们回顾性分析了12例接受CD7 CAR-T细胞治疗的R/R T-ALL/LBL患者的预后。11例患者接受了自体CAR-T细胞,1例患者接受了异基因CAR-T细胞。输注后第28天,67%(8/12)的患者获得了总体缓解(ORR)。中位随访134(14 - 925)天,中位总生存期(OS)为134天,无进展生存期(PFS)为81天。在8例CD7 CAR-T细胞输注后获得缓解的患者中,5例接受了巩固性异基因造血干细胞移植(allo-HSCT)。与3例未接受巩固性allo-HSCT的患者相比,接受allo-HSCT作为巩固治疗的患者在OS(allo-HSCT与对照组:6个月OS,60%对33.3%,p = 0.073)和PFS(allo-HSCT与对照组:6个月PFS,60%对0%,p = 0.022)方面有改善趋势。所有患者均发生了细胞因子释放综合征(CRS)(67%的患者为1 - 2级,33%的患者为3级),1例患者出现神经毒性。CD7 CAR-T细胞疗法对于R/R T-ALL/LBL患者是一个有前景的选择,不良事件可控。此外,R/R T-ALL/LBL患者在CD7 CAR-T细胞输注后进行巩固性allo-HSCT可能在延长缓解期方面发挥重要作用。