[Effect and safety of a conditioning regimen with chidamide and BEAM for autologous hematopoietic stem cell transplantation in lymphoma].

医学 调理疗法 养生 造血干细胞移植 不利影响 外科 累积发病率 内科学 移植 回顾性队列研究 临床试验 肿瘤科 生存分析 总体生存率 累积剂量 存活率 自体干细胞移植 无进展生存期 淋巴瘤 完全响应 随访中值 造血细胞
作者
Yanqiu Gong,S Y Pan,Tingwei Xing,Hang Yin,Hao-Rui Shen,Li Wang,J. Liang,J Y Li,Wei Xu
出处
期刊:PubMed [National Institutes of Health]
卷期号:64 (12): 1211-1217
标识
DOI:10.3760/cma.j.cn112138-20250613-00344
摘要

Objective: To evaluate the efficacy and safety of the Chi-BEAM regimen (chidamide combined with carmustine, etoposide, cytarabine, and melphalan) followed by autologous hematopoietic stem cell transplantation (ASCT) in patients with high-risk or relapsed/refractory lymphoma. Methods: This retrospective case series included 78 patients with newly treated high-risk or relapsed/refractory lymphoma who underwent ASCT with the Chi-BEAM conditioning regimen in the Department of Hematology, the First Affiliated Hospital of Nanjing Medical University (Jiangsu Province Hospital), from June 2021 to May 2024. Descriptive statistics were employed to evaluate clinical characteristics, efficacy, and adverse events. The Kaplan-Meier method was applied to calculate cumulative progression-free survival (PFS) and overall survival (OS) rates. Results: The median age of the 78 evaluable patients was 47 years (range 16-68), with 8 patients (10.3%) aged ≥60 years. At the first post-transplant assessment (3 months), the objective response rate was 94.9% (74/78). The median follow-up was 20.1 months (range 2.9-44.9). The median PFS time was 20.1 months (range 1.6-45.1), with a 2-year cumulative PFS rate of 81.8%. The median OS time was 20.6 months (range 3.1-45.1), with a cumulative 2-year OS rate of 93.2%. The regimen was well-tolerated; mild-to-moderate hypocalcemia within 1 week post-infusion and transient mild erythrocyturia on the infusion day were the primary adverse reactions. Conclusion: The Chi-BEAM regimen combined with ASCT demonstrates both safety and clinical benefit in patients with high-risk or relapsed/refractory lymphoma.
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