Sequential allogeneic HSCT after CAR-T therapy for relapsed/refractory acute lymphoblastic leukemia patients: A long-term follow-up result.

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Tác giả: Alex H Chang, Dawei Cui, Jiazhen Cui, Yetian Dong, Jingjing Feng, Huarui Fu, Shan Fu, Ruimin Hong, Yongxian Hu, He Huang, Simao Huang, Delin Kong, Xiaoyu Lai, Lizhen Liu, Yi Luo, Jimin Shi, Guoqing Wei, Pingnan Xiao, Huijun Xu, Tingting Yang, Yishan Ye, Jian Yu, Mingming Zhang, Yanmin Zhao

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: Egypt : Journal of advanced research , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 94420

 INTRODUCTION: CAR-T cell therapy has revolutionized the therapeutic landscape for relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL), and bridging with allogeneic hematopoietic stem cell transplantation (allo-HSCT) has the potential to lower relapse rates. Nevertheless, the majority of existing studies have exclusively focused on short-term outcomes, resulting in a lack of comprehensive understanding of the long-term sustainability of overall prognosis. OBJECTIVES: Our study aimed to provide real-world, long-term follow-up data for patients who underwent sequential therapy. METHODS: Patients with R/R B-ALL who achieved MRD RESULTS: The median age at transplant of 32.1 years. Of these patients, 88.2 % underwent haploidentical-HSCT, and 11.8 % received either unrelated matched or related matched HSCT. The cumulative incidences of grades I-IV and grade II-IV aGVHD at day 100 were 31.4 % and 15.7 %, respectively. The cumulative incidence of cGVHD at 4 years was 48.3 %. With a median follow-up time of 43.2 months, OS, LFS, and GRFS at 4 years were 68.9 %, 61.4 %, and 39.5 %, respectively. Fifteen cases (29.4 %) experienced relapse, predominantly antigen-positive relapse (n = 11). NRM and CIR at 4 years were 10.6 % and 28.0 %, respectively. In the multivariate analyses, patients over 45 years of age and with poor-risk had significantly dismal OS (P = 0.018
  P = 0.038) and LFS (P = 0.01
  P = 0.03). CONCLUSION: Our study exhibits favorable long-term outcomes consistent with those reported in clinical trials, with sustained, durable responses observed at the 4-year follow-up. However, these benefits are less pronounced in older patients and those with poor-risk disease characteristics.
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