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采用白消安、氟达拉滨和抗胸腺细胞球蛋白的低强度预处理方案行 HLA 单倍体相合造血细胞移植治疗急性白血病和骨髓增生异常综合征。

Reduced-intensity conditioning therapy with busulfan, fludarabine, and antithymocyte globulin for HLA-haploidentical hematopoietic cell transplantation in acute leukemia and myelodysplastic syndrome.

机构信息

Hematology Section, Department of Internal Medicine, University ofUlsan, College of Medicine, Asan Medical Center, Seoul, Korea.

出版信息

Blood. 2011 Sep 1;118(9):2609-17. doi: 10.1182/blood-2011-02-339838. Epub 2011 Jun 28.

Abstract

Any role for reduced-intensity conditioning (RIC) before hematopoietic cell transplantation (HCT) from a human leukocyte antigen (HLA)-haploidentical donor remains to be defined. We therefore assessed 83 patients (age, 16-70 years): 68 with acute leukemia (including 34 in remission and 34 with refractory disease) and 15 patients with myelodysplastic syndrome, in HCT trials using RIC with busulfan, fludarabine, and antithymocyte globulin. The HLA-haploidentical donors, offspring (n = 38), mothers (n = 24), or siblings (n = 21) of patients, underwent leukapheresis after receiving granulocyte colony-stimulating factor, and donated cells were transplanted without further manipulation. Cyclosporine and methotrexate were given for GVHD prophylaxis. The cumulative incidences of neutrophil engraftment, grade 2 to 4 acute GVHD, chronic GVHD, and transplantation-related mortality after HCT, were 92%, 20%, 34%, and 18%, respectively. After a median follow-up time of 26.6 months (range, 16.8-78.8 months), the event-free and overall survival rates were 56% and 45%, respectively, for patients with acute leukemia in remission; 9% and 9%, respectively, for patients with refractory acute leukemia; and 53% and 53%, respectively, for patients with myelodysplastic syndrome. HCT from an HLA-haploidentical family member resulted in favorable outcomes when RIC containing antithymocyte globulin was performed. This study is registered at www.clinicaltrials.gov as #NCT00521430 and #NCT00732316.

摘要

在异基因造血细胞移植(HCT)前采用低强度预处理(RIC)的作用仍有待确定。因此,我们评估了 83 例患者(年龄 16-70 岁):68 例急性白血病(包括 34 例缓解期和 34 例难治性疾病)和 15 例骨髓增生异常综合征患者,这些患者接受了含有白消安、氟达拉滨和抗胸腺细胞球蛋白的 RIC 的 HCT 试验。HLA 单倍体供者,患者的后代(n=38)、母亲(n=24)或兄弟姐妹(n=21),在接受粒细胞集落刺激因子后进行白细胞分离,并在不进行进一步处理的情况下移植细胞。环孢素和甲氨蝶呤用于预防移植物抗宿主病。HCT 后中性粒细胞植入、2-4 级急性移植物抗宿主病、慢性移植物抗宿主病和移植相关死亡率的累积发生率分别为 92%、20%、34%和 18%。中位随访时间为 26.6 个月(范围,16.8-78.8 个月)后,缓解期急性白血病患者的无事件生存率和总生存率分别为 56%和 45%;难治性急性白血病患者分别为 9%和 9%;骨髓增生异常综合征患者分别为 53%和 53%。当使用含有抗胸腺细胞球蛋白的 RIC 进行 HLA 单倍体家族成员的 HCT 时,可获得良好的结果。这项研究在 www.clinicaltrials.gov 上注册为 #NCT00521430 和 #NCT00732316。

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