The Role of Hematopoietic Stem Cell Transplantation in Adults with Acute Myeloid Leukemia

M. Hamadani, W. Blum
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Abstract

Abstract Advances in understanding of the molecular basis of acute myeloid leukemia (AML) are finally beginning to allow tailoring of therapy for patients based on relapse risk. Although remission-induction therapy for most patients today remains predominantly “one-fits-all” cytarabine-based chemotherapy, postremission treatments are becoming more individualized based on cytogenetic or molecular markers of disease. Successive cooperative group trials over the past decade have helped to clarify a role for allogeneic hematopoietic stem cell transplantation (HSCT) for patients with AML in first remission based on cytogenetic risk stratification. More recently, molecular risk stratification has also been helpful in identifying patients who benefit from early transplantation. Herein, we review the current state of allogeneic and autologous HSCT in AML, discuss the role for transplantation in patients with normal-karyotype leukemia, and provide practical recommendations for postremission strategies for AML in first complete remission. We also discuss the role for HSCT in advanced AML, for patients lacking suitable donors, and in older adults with reduced-intensity conditioning.
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造血干细胞移植在成人急性髓性白血病中的作用
对急性髓性白血病(AML)分子基础的理解的进展终于开始允许根据复发风险为患者量身定制治疗。尽管目前大多数患者的缓解诱导治疗仍然主要是“一刀切”的以阿糖胞苷为基础的化疗,但缓解后治疗正变得更加个性化,基于疾病的细胞遗传学或分子标志物。在过去的十年中,连续的合作组试验已经帮助阐明了基于细胞遗传学风险分层的异基因造血干细胞移植(HSCT)在首次缓解的AML患者中的作用。最近,分子风险分层也有助于识别从早期移植中获益的患者。在此,我们回顾了同种异体和自体造血干细胞移植在AML中的现状,讨论移植在正常核型白血病患者中的作用,并为首次完全缓解的AML缓解后策略提供实用建议。我们还讨论了HSCT在晚期AML、缺乏合适供体的患者和低强度调节的老年人中的作用。
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Editorial Board Blood and Bone Marrow Transplantation for Acute Myeloid Leukemia Genomic Lesions Involved in Chronic Myeloid Leukemia Progression Acute Leukemia with M3 Morphology Without Cytogenetic Abnormalities Related to Acute Promyelocytic Leukemia: Description of a Refractory Pediatric Case Salvage of Donor Graft with Decitabine and Maintenance Post Allogeneic Stem Cell Transplantation in Myelodysplastic/Myeloproliferative Disease: A Case Report
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