Allogeneic hematopoietic cell transplantation in acute myeloid leukemia

IF 2.2 4区 医学 Q3 HEMATOLOGY Best Practice & Research Clinical Haematology Pub Date : 2023-06-01 DOI:10.1016/j.beha.2023.101466
Gray Magee, Brittany Knick Ragon
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引用次数: 0

Abstract

Allogeneic hematopoietic cell transplantation (HCT) is a curative treatment modality for select patients with acute myeloid leukemia (AML), functioning as a restorative agent following intensified chemo- and/or radiotherapy and also engendering the disease-directed immunologic threat of graft-versus-leukemia effect. Advancements in conditioning regimen intensity, donor availability, and supportive care have broadened the eligibility for allogeneic HCT, reduced rates of transplant related mortality, and improved outcomes over time. There are still obstacles to transplant in AML, offering opportunities for ongoing discovery, including poor recipient fitness, insufficient donor availability for certain populations, and limited access to care. Relapse remains the most common cause of treatment failure and a high priority area of investigative efforts. Post-transplant maintenance and novel applications of cellular therapeutics are expected to usher in a new era of promise for successful HCT in AML and will aim to overcome the remaining barriers impeding favorable outcomes for these patients.

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异基因造血细胞移植治疗急性髓性白血病
异基因造血细胞移植(HCT)是一种治疗急性髓性白血病(AML)患者的治疗方式,在强化化疗和/或放疗后起到恢复剂的作用,也会产生移植物抗白血病效应的疾病导向性免疫威胁。随着时间的推移,调节方案强度、供体可用性和支持性护理的进步扩大了异基因HCT的适用范围,降低了移植相关死亡率,并改善了结果。AML的移植仍然存在障碍,这为不断的发现提供了机会,包括接受者身体状况不佳、某些人群的供体可用性不足以及获得护理的机会有限。复发仍然是治疗失败的最常见原因,也是调查工作的高度优先领域。移植后的维持和细胞疗法的新应用有望为AML的HCT成功开辟一个充满希望的新时代,并将致力于克服阻碍这些患者获得良好结果的剩余障碍。
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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Best Practice & Research Clinical Haematology publishes review articles integrating the results from the latest original research articles into practical, evidence-based review articles. These articles seek to address the key clinical issues of diagnosis, treatment and patient management. Each issue follows a problem-orientated approach which focuses on the key questions to be addressed, clearly defining what is known and not known, covering the spectrum of clinical and laboratory haematological practice and research. Although most reviews are invited, the Editor welcomes suggestions from potential authors.
期刊最新文献
Erratum to “Special issue 37.2 and 37.3 Genetics and Function of HLA and immune-related genes in transplantation and cellular immunotherapy” [Best Pract Res Clin Haematol (2024) 101588] Editorial Board From clones to immunopeptidomes: New developments in the characterization of permissive HLA-DP mismatches in hematopoietic cell transplantation Relevance of donor-specific HLA antibodies in hematopoietic cell transplantation HLA structure and function in hematopoietic-cell transplantation
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