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Allogeneic bone marrow transplantation from partially mismatched related donors as therapy for primary induction failure acute myeloid leukemia.

机译:部分不匹配的相关供体的同种异体骨髓移植作为原发性诱导衰竭急性髓细胞白血病的治疗方法。

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The outcome of acute myeloid leukemia patients with primary refractoriness to conventional chemotherapy is extremely poor. Allogeneic bone marrow transplants with matched sibling or matched unrelated donors provide 10-20% disease-free survival in this setting. We analyzed our transplant experience using readily available partially mismatched related donor (PMRD) in patients with primary induction failure (PIF) AML. Between March 1994 and December 1998, 13 patients with PIF AML were transplanted from 0-3 HLA antigen mismatched donors. All 12 evaluable patients engrafted at a median of day +16. Ten (77%) patients survived at least 100 days after transplant. Acute GVHD (grade II) was observed in one of 12 patients. Chronic GVHD was seen in one of 10 patients surviving beyond day 100. The major cause of failure was relapse of disease in six occurring 3-12 months after PMRD BMT. Three patients are alive without disease 14, 36 and 45 months post BMT with Karnofsky scores of 100%. The actuarial 3-year probabilities of relapse and disease-free survival were 0.54 and 0.19, respectively. We concluded that a PMRD graft is a viable option, comparable to the use of matched related or unrelated donors, in patients with PIF AML in whom time is of the essence.
机译:急性髓细胞性白血病患者对传统化学疗法具有主要难治性,结果非常差。在这种情况下,具有相匹配的同胞或相匹配的不相关供体的同种异体骨髓移植可提供10-20%的无病生存率。我们分析了在原发性诱导衰竭(PIF)AML患者中使用易得的部分不匹配相关供体(PMRD)的移植经验。在1994年3月至1998年12月之间,从0-3 HLA抗原错配的供体中移植了13例PIF AML患者。所有12位可评估患者在第16天的中位数移植。十名(77%)患者在移植后至少存活了100天。在12名患者中的1名患者中观察到了急性GVHD(II级)。存活超过100天的10例患者中有1例发现了慢性GVHD。失败的主要原因是PMRD BMT后3-12个月内发生的6例疾病复发。 BMT后14、36和45个月有3例患者没有疾病存活,Karnofsky评分为100%。 3年精算复发率和无病生存率分别为0.54和0.19。我们得出的结论是,对于时间至关重要的PIF AML患者,与使用匹配的相关或不相关的供体相比,PMRD移植是一种可行的选择。

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