首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Reduced-intensity conditioning therapy with busulfan, fludarabine, and antithymocyte globulin for HLA-haploidentical hematopoietic cell transplantation in acute leukemia and myelodysplastic syndrome.
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Reduced-intensity conditioning therapy with busulfan, fludarabine, and antithymocyte globulin for HLA-haploidentical hematopoietic cell transplantation in acute leukemia and myelodysplastic syndrome.

机译:在急性白血病和骨髓增生异常综合症中使用白消安,氟达拉滨和抗胸腺细胞球蛋白降低强度的调理疗法,用于HLA单倍型造血细胞移植。

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摘要

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.
机译:从人类白细胞抗原(HLA)单倍体供体进行造血细胞移植(HCT)之前降低强度调节(RIC)的任何作用仍有待确定。因此,在HRIC试验中,我们在RIC联合白硫丹,氟达拉滨和抗胸腺细胞球蛋白的HCT试验中,我们评估了83例患者(年龄16-70岁):68例急性白血病(包括34例缓解和34例难治性疾病)和15例骨髓增生异常综合征患者。接受粒细胞集落刺激因子后接受白细胞分离术的患者的HLA单倍体供体,后代(n = 38),母亲(n = 24)或兄弟姐妹(n = 21),无需进一步操作即可移植捐赠的细胞。给予环孢霉素和甲氨蝶呤预防GVHD。 HCT后中性粒细胞植入,2-4级急性GVHD,慢性GVHD和移植相关死亡率的累积发生率分别为92%,20%,34%和18%。在中位随访时间为26.6个月(范围为16.8-78.8个月)之后,急性白血病缓解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%;骨髓增生异常综合症患者分别为53%和53%。当进行含抗胸腺细胞球蛋白的RIC时,来自HLA单亲家庭成员的HCT产生了良好的结果。该研究已在www.clinicaltrials.gov上注册为#NCT00521430和#NCT00732316。

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