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骨髓增生异常综合征所致急性髓系白血病的 upfront 异基因造血细胞移植

Up-front allogeneic hematopoietic cell transplantation in acute myeloid leukemia arising from the myelodysplastic syndrome.

作者信息

Choi Yunsuk, Kim Sung-Doo, Park Young-Hoon, Lee Jae Seok, Kim Dae-Young, Lee Jung-Hee, Lee Kyoo-Hyung, Seol Miee, Lee Young-Shin, Kang Young-Ah, Jeon Mijin, Jung Ah Rang, Lee Je-Hwan

机构信息

Department of Hematology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Acta Haematol. 2015;133(2):183-92. doi: 10.1159/000362260. Epub 2014 Oct 11.

DOI:10.1159/000362260
PMID:25323649
Abstract

In patients with secondary acute myeloid leukemia (s-AML) arising from the myelodysplastic syndrome (MDS), treatment outcome is unsatisfactory. We compared up-front allogeneic hematopoietic cell transplantation (HCT) to induction chemotherapy (IC) as an initial treatment in patients with s-AML arising from MDS. This retrospective study included 85 patients who were diagnosed with s-AML arising from MDS; 11 patients proceeded to up-front HCT without IC (HCT group) and 74 received IC (IC group) as an initial treatment for s-AML, 28 of whom subsequently underwent HCT. In the IC group, 41.9% achieved complete remission (CR) compared to 81.8% in the HCT group (p = 0.013). The HCT group showed a significantly longer event-free survival (EFS) than the IC group (median 29.2 vs. 5.2 months, p = 0.042). Overall survival of the HCT group was higher than that of the IC group, but the difference was not statistically significant (median 34.6 vs. 7.6 months, p = 0.149). After adjustment for other clinical factors, outcome in the HCT group was significantly better than in the IC group in terms of CR rate (hazard ratio, HR, 11.195; p = 0.007) and EFS (HR, 0.384; p = 0.029). Up-front HCT is a viable option in s-AML arising from MDS if an appropriate donor is available.

摘要

在由骨髓增生异常综合征(MDS)引发的继发性急性髓系白血病(s-AML)患者中,治疗效果并不理想。我们比较了直接进行异基因造血细胞移植(HCT)与诱导化疗(IC)作为MDS相关s-AML患者的初始治疗方法。这项回顾性研究纳入了85例被诊断为MDS相关s-AML的患者;11例患者直接进行HCT而未接受IC(HCT组),74例接受IC(IC组)作为s-AML的初始治疗,其中28例随后接受了HCT。在IC组中,41.9%的患者实现了完全缓解(CR),而HCT组为81.8%(p = 0.013)。HCT组的无事件生存期(EFS)明显长于IC组(中位数分别为29.2个月和5.2个月,p = 0.042)。HCT组的总生存期高于IC组,但差异无统计学意义(中位数分别为34.6个月和7.6个月,p = 0.149)。在对其他临床因素进行调整后,HCT组在CR率(风险比,HR,11.195;p = 0.007)和EFS(HR,0.384;p = 0.029)方面的结局明显优于IC组。如果有合适的供体,直接进行HCT是MDS相关s-AML的一个可行选择。

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