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Alternative Donor Allogeneic Hematopoietic Cell Transplantation for Acute Myeloid Leukemia

机译:急性髓样白血病的替代供体同种异体造血细胞移植。

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Allogeneic hematopoietic cell transplantation (alloHCT) provides a potentially curative therapy for patients with high-risk or chemorefractory acute myeloid leukemia (AML). Historically, the applicability of alloHCT has been limited as only 30%-35% of patients have human leukocyte antigen (HLA)matched siblings and outcomes using other donor types have been markedly inferior due to excess toxicity, graft failure, graft-versus-host disease (GVHD), and consequently non-relapse mortality. Advances in HLA typing, GVHD prophylactic approaches, and other transplantation techniques have successfully addressed these historical challenges. Herein, we review recent alloHCT studies using volunteer unrelated donors, umbilical cord blood units, or HLA-haploidentical donors, specifically focusing on studies that compared outcomes between donor sources. Although none are randomized and most are retrospective, these analyses suggest that current outcomes for AML patients using most alternative donor types are comparable to those seen using HLA-matched siblings. Published by Elsevier Inc.
机译:同种异体造血细胞移植(alloHCT)为高风险或化学难治性急性髓细胞性白血病(AML)患者提供了潜在的治疗方法。从历史上看,alloHCT的适用性受到限制,因为只有30%-35%的患者患有人类白细胞抗原(HLA)匹配的兄弟姐妹,并且由于毒性过大,移植失败,移植物抗宿主,使用其他供体类型的结果明显较差疾病(GVHD),从而导致非复发死亡率。 HLA分型,GVHD预防方法和其他移植技术的进步已成功解决了这些历史挑战。本文中,我们回顾了近期使用志愿无关亲属,脐带血单位或HLA单倍体供体的alloHCT研究,特别侧重于比较供体来源之间结果的研究。尽管没有一个是随机分组的,而且大多数是回顾性的,但这些分析表明,使用大多数其他供体类型的AML患者的当前结局与使用HLA匹配的同胞所观察到的结果相当。由Elsevier Inc.发布

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