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Retrospective study of allogeneic haematopoietic stem-cell transplantation for myelofibrosis.

机译:骨髓纤维化同种异体造血干细胞移植的回顾性研究。

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摘要

Allogeneic haematopoietic stem-cell transplantation (HSCT) is the only curative treatment for myelofibrosis. We retrospectively analyzed the outcome of patients who underwent allogeneic HSCT, 1994-2008, and the potential risk factors affecting non-relapse mortality (NRM), OS and relapse-free survival (RFS). A total of 39 patients, 15-65 (median 49) years old, diagnosed with primary (n=27) or secondary (n=12) myelofibrosis underwent HSCT (25 related and 14 unrelated). In ten patients, disease had transformed into acute leukaemia. Lille prognosis score was low for 9, intermediate for 16 and high for 14 patients. The conditioning regimen was myeloablative (MAC) for 15 and reduced-intensity (RIC) fludarabine-based for 24, with successful engraftment in 38 patients. A total of 31 patients developed grade I-IV GvHD; 19 developed chronic GvHD. The 3-year OS, RFS and NRM rates (95% confidence interval) were 60% (42-74), 54% (37-59) and 30% (30-45), respectively.
机译:异基因造血干细胞移植(HSCT)是治疗骨髓纤维化的唯一方法。我们回顾性分析了1994-2008年接受异基因HSCT的患者的结局,以及影响非复发死亡率(NRM),OS和无复发生存率(RFS)的潜在危险因素。总共39例15-65岁(中位数49岁)的被诊断为原发性(n = 27)或继发性(n = 12)骨髓纤维化的患者接受了HSCT(25例相关,14例无关)。在十名患者中,疾病已转变为急性白血病。里尔的预后评分为9分低,中级16位和14位高。调理方案为清髓性(MAC)治疗15例,降强度(RIC)氟达拉滨治疗24例,成功植入38例患者。共有31名患者发展了I-IV级GvHD。 19例发展为慢性GvHD。 3年OS,RFS和NRM率(95%置信区间)分别为60%(42-74),54%(37-59)和30%(30-45)。

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