Kanate Abraham S, Pasquini Marcelo C, Hari Parameswaran N, Hamadani Mehdi
Abraham S Kanate, Osborn Hematopoietic Malignancy and Transplantation program, Section of Hematology/Oncology, West Virginia University, Morgantown, WV 26506, United States.
World J Stem Cells. 2014 Apr 26;6(2):69-81. doi: 10.4252/wjsc.v6.i2.69.
Acute myeloid leukemia (AML) represents a heterogeneous group of high-grade myeloid neoplasms of the elderly with variable outcomes. Though remission-induction is an important first step in the management of AML, additional treatment strategies are essential to ensure long-term disease-free survival. Recent pivotal advances in understanding the genetics and molecular biology of AML have allowed for a risk-adapted approach in its management based on relapse-risk. Allogeneic hematopoietic cell transplantation (allo-HCT) represents an effective therapeutic strategy in AML providing the possibility of cure with potent graft-versus-leukemia reactions, with a demonstrable survival advantage in younger patients with intermediate- or poor-risk cytogenetics. Herein we review the published data regarding the role of allo-HCT in adults with AML. We searched MEDLINE/PubMed and EMBASE/Ovid. In addition, we searched reference lists of relevant articles, conference proceedings and ongoing trial databases. We discuss the role of allo-HCT in AML patients stratified by cytogenetic- and molecular-risk in first complete remission, as well as allo-HCT as an option in relapsed/refractory AML. Besides the conventional sibling and unrelated donor allografts, we review the available data and recent advances for alternative donor sources such as haploidentical grafts and umbilical cord blood. We also discuss conditioning regimens, including reduced intensity conditioning which has broadened the applicability of allo-HCT. Finally we explore recent advances and future possibilities and directions of allo-HCT in AML. Practical therapeutic recommendations have been made where possible based on available data and expert opinion.
急性髓系白血病(AML)是一组异质性的老年高级别髓系肿瘤,预后各异。虽然诱导缓解是AML治疗的重要第一步,但额外的治疗策略对于确保长期无病生存至关重要。最近在理解AML的遗传学和分子生物学方面取得的关键进展,使得基于复发风险的风险适应性治疗方法在其管理中得以应用。异基因造血细胞移植(allo-HCT)是AML的一种有效治疗策略,通过强大的移植物抗白血病反应提供治愈的可能性,在具有中危或高危细胞遗传学特征的年轻患者中具有明显的生存优势。在此,我们综述了已发表的关于allo-HCT在成人AML中作用的数据。我们检索了MEDLINE/PubMed和EMBASE/Ovid。此外,我们还检索了相关文章的参考文献列表、会议论文集和正在进行的试验数据库。我们讨论了allo-HCT在首次完全缓解时按细胞遗传学和分子风险分层的AML患者中的作用,以及allo-HCT作为复发/难治性AML的一种选择。除了传统的同胞和无关供体移植外,我们还综述了单倍体相合移植物和脐带血等替代供体来源的现有数据和最新进展。我们还讨论了预处理方案,包括降低强度预处理,这拓宽了allo-HCT的适用性。最后,我们探讨了allo-HCT在AML中的最新进展以及未来的可能性和方向。在可能的情况下,已根据现有数据和专家意见提出了实用的治疗建议。