College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Hematology, Catholic Hematology Hospital and Leukemia Research Institute, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Bone Marrow Transplant. 2024 Oct;59(10):1413-1422. doi: 10.1038/s41409-024-02363-7. Epub 2024 Jul 12.
Reduced-toxicity conditioning (RTC) regimens aim to mitigate regimen-related toxicity while maintaining anti-leukemic efficacy in allogeneic hematopoietic stem cell transplantation (allo-HSCT). We assessed outcomes of RTC regimens utilizing melphalan versus intravenous busulfan combined with fludarabine in adult acute lymphoblastic leukemia (ALL) patients. A retrospective analysis was conducted with 149 consecutive adult ALL patients (median age 51, range 18-60) in remission undergoing allo-HSCT. Patients received either fludarabine 150 mg/BSA plus 2 days of melphalan 70 mg/BSA (FM140, n = 76) from 2009 to 2015 or fludarabine plus 3 days of busulfan 3.2 mg/kg (FB9.6, n = 73) from 2016 to 2021. At 5 years post-HSCT, FM140 demonstrated superior disease-free survival (53.4% vs. 30.5%, p = 0.007) and lower cumulative relapse (27.4% vs. 46.8%, p = 0.026) than FB9.6. Five-year overall survival and non-relapse mortality did not significantly differ. FM140 exhibited a higher incidence of acute graft-versus-host disease (GVHD) grades II-IV (49.3% vs. 30.3%, p = 0.016), though rates of acute GVHD grades III-IV and chronic GVHD were similar. Multivariate analysis identified Philadelphia chromosome and minimal residual disease positive status, and FB9.6 conditioning as predictors of increased relapse and poorer disease-free survival. FM140 RTC regimen displayed significantly reduced relapse and superior disease-free survival compared to FB9.6 in ALL patients undergoing allo-HSCT, highlighting its current clinical utility.
减毒预处理(RTC)方案旨在减轻治疗相关毒性,同时保持异基因造血干细胞移植(allo-HSCT)中的抗白血病疗效。我们评估了在成人急性淋巴细胞白血病(ALL)患者中,使用美法仑与静脉用白消安联合氟达拉滨的 RTC 方案的结果。对 149 例缓解期接受 allo-HSCT 的连续成人 ALL 患者进行回顾性分析。患者接受氟达拉滨 150mg/BSA 加 2 天美法仑 70mg/BSA(FM140,n=76)治疗,或氟达拉滨加 3 天白消安 3.2mg/kg(FB9.6,n=73)治疗,时间分别为 2009 年至 2015 年和 2016 年至 2021 年。HSCT 后 5 年,FM140 组无病生存率(53.4% vs. 30.5%,p=0.007)优于 FB9.6 组,累积复发率(27.4% vs. 46.8%,p=0.026)低于 FB9.6 组。5 年总生存率和非复发死亡率无显著差异。FM140 组急性移植物抗宿主病(GVHD)Ⅱ-Ⅳ级发生率较高(49.3% vs. 30.3%,p=0.016),但急性 GVHD Ⅲ-Ⅳ级和慢性 GVHD 发生率相似。多变量分析显示,费城染色体和微小残留病阳性状态以及 FB9.6 预处理是复发和无病生存率降低的预测因素。FM140 RTC 方案在 ALL 患者 allo-HSCT 中较 FB9.6 显著降低复发率和提高无病生存率,突出了其目前的临床应用价值。