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骨髓增生异常综合征和继发性急性髓系白血病中自体与非亲缘供者造血细胞移植的回顾性比较:代表欧洲血液与骨髓移植组(EBMT)慢性白血病工作组的报告

A retrospective comparison of autologous and unrelated donor hematopoietic cell transplantation in myelodysplastic syndrome and secondary acute myeloid leukemia: a report on behalf of the Chronic Leukemia Working Party of the European Group for Blood and Marrow Transplantation (EBMT).

作者信息

Al-Ali H K, Brand R, van Biezen A, Finke J, Boogaerts M, Fauser A A, Egeler M, Cahn J-Y, Arnold R, Biersack H, Niederwieser D, de Witte T

机构信息

Department of Hematology/Oncology, University of Leipzig, Leipzig, Germany.

出版信息

Leukemia. 2007 Sep;21(9):1945-51. doi: 10.1038/sj.leu.2404774. Epub 2007 Jul 5.

Abstract

Hematopoietic cell transplantation (HCT) is an effective treatment for myelodysplasia (MDS) and secondary acute myeloid leukemia (sAML). In this study, outcome of 593 patients with MDS/sAML after autologous and allogeneic HCT from a matched unrelated donor (MUD) were compared. A total of 167 (28%) patients received HCT from MUD without prior chemotherapy (MUD-U). The rest received HCT in first complete remission (CR1) (Autologous (Auto-CR1), n=290 (49%), HCT from MUD (MUD-CR1), n=136 (23%)). Survival at 3 years was best in MUD-CR1 (50%) compared to Auto-CR1 (41%) and MUD-U (40%) (P=0.01). Similarly, disease-free survival was 44% for MUD-CR1 compared to Auto-CR1 (28%) and MUD-U (34%) (P=0.03). Treatment-related mortality was 17% in Auto-CR1 compared to MUD-CR1 (38%) and MUD-U (49%) (P<0.001). Relapse for Auto-CR1 was 62% compared to 24 and 30% for MUD-CR1 and MUD-U, respectively (P<0.001). Outcome was best for patients with low tumor burden transplanted 6-12 months after diagnosis. Factors influencing outcome at 3 years were mainly significant in the first 6 months. Only, relapse after autologous HCT remained constant over time. Outcomes after allogeneic HCT in patients of 20-40 and >40 years were similar. Autologous and Allogeneic HCT from MUD offer the possibility of long-term survival to patients with MDS/sAML.

摘要

造血细胞移植(HCT)是治疗骨髓增生异常综合征(MDS)和继发性急性髓系白血病(sAML)的有效方法。在本研究中,对593例MDS/sAML患者接受来自匹配无关供者(MUD)的自体和异基因HCT后的结局进行了比较。共有167例(28%)患者在未进行过化疗的情况下接受了来自MUD的HCT(MUD-U)。其余患者在首次完全缓解(CR1)时接受了HCT(自体(Auto-CR1),n = 290例(49%),来自MUD的HCT(MUD-CR1),n = 136例(23%))。3年生存率在MUD-CR1组最佳(50%),相比之下Auto-CR1组为41%,MUD-U组为40%(P = 0.01)。同样,MUD-CR1组的无病生存率为44%,相比之下Auto-CR1组为28%,MUD-U组为34%(P = 0.03)。Auto-CR1组的治疗相关死亡率为17%,相比之下MUD-CR1组为38%,MUD-U组为49%(P<0.001)。Auto-CR1组的复发率为62%,相比之下MUD-CR1组和MUD-U组分别为24%和30%(P<0.001)。诊断后6 - 12个月进行移植的低肿瘤负荷患者结局最佳。影响3年结局的因素主要在前6个月较为显著。仅自体HCT后的复发率随时间保持稳定。20 - 40岁和>40岁患者接受异基因HCT后的结局相似。来自MUD的自体和异基因HCT为MDS/sAML患者提供了长期生存的可能性。

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