首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Allogeneic stem cell transplantation after reduced-intensity conditioning in patients with myelofibrosis: a prospective, multicenter study of the Chronic Leukemia Working Party of the European Group for Blood and Marrow Transplantation.
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Allogeneic stem cell transplantation after reduced-intensity conditioning in patients with myelofibrosis: a prospective, multicenter study of the Chronic Leukemia Working Party of the European Group for Blood and Marrow Transplantation.

机译:骨髓纤维化患者降低强度条件后的同种异体干细胞移植:欧洲​​血液和骨髓移植小组慢性白血病工作组的一项前瞻性,多中心研究。

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From 2002 to 2007, 103 patients with primary myelofibrosis or postessential thrombocythemia and polycythemia vera myelofibrosis and a median age of 55 years (range, 32-68 years) were included in a prospective multicenter phase 2 trial to determine efficacy of a busulfan (10 mg/kg)/fludarabine (180 mg/m(2))-based reduced-intensity conditioning regimen followed by allogeneic stem cell transplantation from related (n = 33) or unrelated donors (n = 70). All but 2 patients (2%) showed leukocyte and platelet engraftment after a median of 18 and 22 days, respectively. Acute graft-versus-host disease grade 2 to 4 occurred in 27% and chronic graft-versus-host disease in 43% of the patients. Cumulative incidence of nonrelapse mortality at 1 year was 16% (95% confidence interval, 9%-23%) and significantly lower for patients with a completely matched donor (12% vs 38%; P = .003). The cumulative incidence of relapse at 3 years was 22% (95% confidence interval, 13%-31%) and was influenced by Lille risk profile (low, 14%; intermediate, 22%; and high, 34%; P = .02). The estimated 5-year event-free and overall survival was 51% and 67%, respectively. In a multivariate analysis, age older than 55 years (hazard ratio = 2.70; P = .02) and human leukocyte antigen-mismatched donor (hazard ratio = 3.04; P = .006) remained significant factors for survival. The study was registered at www.clinicaltrials.gov as #NCT 00599547.
机译:从2002年到2007年,一项前瞻性多中心2期试验纳入了103例原发性骨髓纤维化或后继发性血小板增多症和真性红细胞增多症的真性骨髓纤维化患者,中位年龄为55岁(范围32-68岁),以测定白消安的疗效(10 mg / kg)/氟达拉滨(180 mg / m(2))为基础的降低强度条件治疗方案,然后从相关(n = 33)或无关的供体(n = 70)进行同种异体干细胞移植。除2名患者(2%)外,其余所有患者均在中位数分别为18天和22天后出现白细胞和血小板移植。 27%的患者发生2至4级急性移植物抗宿主病,43%的患者发生慢性移植物抗宿主病。一年内非复发死亡率的累积发生率为16%(95%置信区间,9%-23%),而完全匹配供体的患者则显着降低(12%对38%; P = 0.003)。 3年时复发的累积发生率是22%(95%置信区间,13%-31%),并受里尔风险状况的影响(低14%;中级22%;高34%; P =)。 02)。估计的5年无事件生存率和总生存率分别为51%和67%。在多变量分析中,年龄大于55岁(危险比= 2.70; P = .02)和人白细胞抗原不匹配的供体(危险比= 3.04; P = .006)仍然是存活的重要因素。该研究已在www.clinicaltrials.gov上注册为#NCT 00599547。

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