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接受了550 cGy全身照射和环磷酰胺的减低强度预处理方案后进行异基因移植的骨髓增生异常综合征和继发性急性髓系白血病患者的长期缓解情况。

Long-term remissions in patients with myelodysplastic syndrome and secondary acute myelogenous leukemia undergoing allogeneic transplantation following a reduced intensity conditioning regimen of 550 cGy total body irradiation and cyclophosphamide.

作者信息

Hallemeier Christopher L, Girgis Mark D, Blum William G, Brown Randy A, Khoury Hanna J, Devine Steven M, Vij Ravi, Lin Hsu-san, DiPersio John F, Adkins Douglas R

机构信息

Department of Internal Medicine, Division of Oncology, Section of Bone Marrow Transplantation and Leukemia, St Louis, Missouri, USA.

出版信息

Biol Blood Marrow Transplant. 2006 Jul;12(7):749-57. doi: 10.1016/j.bbmt.2006.03.009.

Abstract

We analyzed outcomes of patients with myelodysplastic syndrome (MDS) or secondary acute myelogenous leukemia (sAML) that were treated at our institution with a reduced intensity conditioning (RIC) regimen of 550-cGy total body irradiation and cyclophosphamide followed by related donor (RD) or unrelated donor (URD) transplantation. Fifty-one consecutive patients with MDS or sAML received this RIC regimen and URD (n = 30) or RD (n = 21) stem cells. Graft-versus-host disease prophylaxis consisted of cyclosporine alone (RD) or with corticosteroids and methotrexate (URD). Median patient age was 44 years. With a median follow-up of 3.7 years after transplantation in the 19 surviving patients (37%), Kaplan-Meier estimates of overall survival were 88%, 46%, 33%, and 11% for patients transplanted with sAML in remission, refractory anemia, refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, or sAML refractory/untreated, respectively. Kaplan-Meier estimates of relapse-free survival were 75%, 46%, 33%, and 11%, respectively. Overall, the cumulative incidences of relapse and transplant-related mortality were 27% and 37%, respectively. In patients with MDS, this is an effective RIC regimen for allogeneic transplantation that can be used as an alternative to other RIC or conventional conditioning regimens.

摘要

我们分析了在我院接受550 cGy全身照射和环磷酰胺的减低强度预处理(RIC)方案,随后进行相关供者(RD)或无关供者(URD)移植治疗的骨髓增生异常综合征(MDS)或继发性急性髓系白血病(sAML)患者的预后。51例连续的MDS或sAML患者接受了该RIC方案及URD(n = 30)或RD(n = 21)干细胞移植。移植物抗宿主病预防措施为单独使用环孢素(RD)或联合使用皮质类固醇和甲氨蝶呤(URD)。患者中位年龄为44岁。19例存活患者(37%)移植后中位随访3.7年,对于移植时处于缓解期的sAML、难治性贫血、伴有过多原始细胞的难治性贫血、转化中的伴有过多原始细胞的难治性贫血或难治/未治疗的sAML患者,Kaplan-Meier总体生存估计分别为88%、46%、33%和11%。Kaplan-Meier无复发生存估计分别为75%、46%、33%和11%。总体而言,复发和移植相关死亡率的累积发生率分别为27%和37%。对于MDS患者,这是一种有效的异基因移植RIC方案,可作为其他RIC或传统预处理方案的替代方案。

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