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采用大剂量白消安和环磷酰胺(BU-CY)作为预处理方案进行无关供者异基因骨髓移植。

Unrelated allogeneic bone marrow transplantation using high-dose busulfan and cyclophosphamide (BU-CY) for the preparative regimen.

作者信息

Sahebi F, Copelan E, Crilley P, Bolwell B, Avalos B, Klein J, Territo M, Gajewski J

机构信息

Transplantation Biology Unit, UCLA Hospital and Clinics, USA.

出版信息

Bone Marrow Transplant. 1996 May;17(5):685-9.

PMID:8733682
Abstract

This study reviews results of a radiation-free preparative regimen consisting of busulfan and cyclophosphamide in 65 unrelated allogeneic bone marrow transplant recipients. Thirty-eight patients had chronic myelogenous leukemia (17 patients chronic phase, 13 patients accelerated phase, eight patients blast phase), 19 patients had acute leukemia (second complete remission or relapse) and eight patients had myelodysplasia. The patients were transplanted at four different medical centers from July 1988 to November 1992. Ages ranged 4-48 years (median 32). Fifty-seven patients received busulfan 16 mg/kg and cyclophosphamide 120 mg/kg, and eight received busulfan at doses between 15 and 17 mg/kg and cyclophosphamide at doses 100-200 mg/kg as preparative regimens. All patients received cyclosporine for graft-versus-host disease prophylaxis; in addition 46 patients received corticosteroid, 38 methotrexate, six anti-CD5 ricin A-immunotoxin, and four T cell-depleted bone marrow. Median follow-up of survivors was 53 months (range 15-68 months). Four year actuarial survival was 24 +/- 12%. Four-year survival based on disease was 29 +/- 27% for chronic myelogenous leukemia (CML) in chronic phase, 20 +/- 9% for chronic myelogenous leukemia in accelerated phase, 0% for chronic myelogenous leukemia in blast phase, 32 +/- 40% for acute leukemia, and 38 +/- 34% for myelodysplasia. Actuarial survival was 66 +/- 40% in patients age < 20 years, vs 23 +/- 13% for patients ages 20 to 40, and 10 +/- 14% for patients age > 40 years. Fifty patients (88%) engrafted. Graft failure occurred in eight patients. Acute graft-versus-host disease grade II-IV occurred in 36 (72%). Two patients relapsed after engraftment with the donor cells and died of leukemia within a month of relapse. The most common causes of death were graft-versus-host disease (37%), and transplant-related toxicity (59%); relapse (4%) was a rare cause of death. Busulfan/cyclophosphamide is an effective preparative regimen in unrelated bone marrow transplantation permitting adequate engraftment and a low relapse rate. Best results are observed in patients less than 20 years old.

摘要

本研究回顾了65例非亲缘异基因骨髓移植受者接受由白消安和环磷酰胺组成的无辐射预处理方案的结果。38例患者患有慢性粒细胞白血病(17例慢性期,13例加速期,8例急变期),19例患者患有急性白血病(第二次完全缓解或复发),8例患者患有骨髓增生异常综合征。这些患者于1988年7月至1992年11月在四个不同的医疗中心接受移植。年龄范围为4至48岁(中位数32岁)。57例患者接受白消安16mg/kg和环磷酰胺120mg/kg,8例患者接受白消安剂量为15至17mg/kg和环磷酰胺剂量为100 - 200mg/kg作为预处理方案。所有患者均接受环孢素预防移植物抗宿主病;此外,46例患者接受了皮质类固醇,38例接受了甲氨蝶呤,6例接受了抗CD5蓖麻毒素A免疫毒素,4例接受了T细胞去除的骨髓。存活者的中位随访时间为53个月(范围15 - 68个月)。四年精算生存率为24±12%。基于疾病的四年生存率,慢性期慢性粒细胞白血病(CML)为29±27%,加速期慢性粒细胞白血病为20±9%,急变期慢性粒细胞白血病为0%,急性白血病为32±40%,骨髓增生异常综合征为38±34%。年龄<20岁的患者精算生存率为66±40%,20至40岁的患者为23±13%,年龄>40岁的患者为10±14%。50例患者(88%)植入成功。8例患者发生移植失败。36例(72%)发生II - IV级急性移植物抗宿主病。2例患者在植入供体细胞后复发,并在复发后一个月内死于白血病。最常见的死亡原因是移植物抗宿主病(37%)和移植相关毒性(59%);复发(4%)是罕见的死亡原因。白消安/环磷酰胺是一种有效的非亲缘骨髓移植预处理方案,可实现充分植入且复发率低。在年龄小于20岁的患者中观察到最佳结果。

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