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异基因骨髓移植:92例患者的经验。

Allogeneic bone marrow transplantation: experience with 92 patients.

作者信息

Selby G B, Saez R A, Epstein R B, Slease R B, Confer D L

机构信息

University of Oklahoma Health Sciences Center.

出版信息

J Okla State Med Assoc. 1993 Dec;86(12):599-603.

PMID:8126587
Abstract

Allogeneic bone marrow transplantation (BMT) is potentially curative therapy for leukemia, lymphoma, and marrow failure. Ninety-two patients have received allogeneic BMT at Oklahoma Memorial Hospital in the past 10 years. Patients with acute myelogenous leukemia (AML; N = 30), chronic myelogenous leukemia (CML; N = 27), acute lymphoblastic leukemia (ALL; N = 12), myelodysplastic syndromes (MDS; N = 8), lymphomas (N = 8), and aplastic anemia (N = 7) were treated with a variety of myeloablative preparative regimens. The major causes of mortality were bacterial, viral, and fungal infections, or disease relapse. Standard and high risk (refractory or multiply-relapsed disease) AML, CML, and ALL patients had median survivals of 14.5 months vs. 3 months, > 18 months vs. 9 months, and 10 months vs. 4.5 months (p = 0.01), respectively. At 7.5 years median follow-up, 71% of the aplastic anemia patients are disease-free. Guidelines for the optimal time for BMT have been developed that encourage transplantation earlier in the course of the disease, thus facilitating better outcomes with these otherwise fatal disorders.

摘要

异基因骨髓移植(BMT)是治疗白血病、淋巴瘤和骨髓衰竭的一种潜在的根治性疗法。在过去10年中,有92名患者在俄克拉荷马纪念医院接受了异基因BMT。患有急性髓细胞白血病(AML;n = 30)、慢性髓细胞白血病(CML;n = 27)、急性淋巴细胞白血病(ALL;n = 12)、骨髓增生异常综合征(MDS;n = 8)、淋巴瘤(n = 8)和再生障碍性贫血(n = 7)的患者接受了多种清髓性预处理方案的治疗。死亡的主要原因是细菌、病毒和真菌感染或疾病复发。标准风险和高风险(难治性或多次复发疾病)的AML、CML和ALL患者的中位生存期分别为14.5个月对3个月、> 18个月对9个月、10个月对4.5个月(p = 0.01)。在中位随访7.5年时,71%的再生障碍性贫血患者无病生存。已经制定了BMT最佳时机的指南,鼓励在疾病过程中尽早进行移植,从而使这些原本致命的疾病获得更好的治疗效果。

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