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高危急性髓系白血病异基因造血细胞移植后预防复发的缓解后策略:欧洲血液和骨髓移植学会急性白血病工作组的专家评论。

Post-remission strategies for the prevention of relapse following allogeneic hematopoietic cell transplantation for high-risk acute myeloid leukemia: expert review from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation.

机构信息

Utah Blood and Marrow Transplant Program, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

Bone Marrow Transplant. 2019 Apr;54(4):519-530. doi: 10.1038/s41409-018-0286-2. Epub 2018 Aug 13.

DOI:10.1038/s41409-018-0286-2
PMID:30104717
Abstract

Acute myeloid leukemia (AML) is an aggressive hematopoietic malignancy generally associated with poor prognosis. Allogeneic hematopoietic cell transplantation (alloHCT) continues to be the most potent anti-leukemia treatment for adult patients with intermediate and high-risk AML. However, disease relapse after alloHCT remains unacceptably high and is the primary cause of treatment failure and mortality following alloHCT. It is therefore that post-transplant early cellular or pharmacologic maintenance or preemptive strategies to enhance the graft-versus-leukemia effect or to eradicate persistent minimal residual disease have been of renewed interest, particularly with the availability of more sensitive technologies to measure residual AML. Although preliminary studies have demonstrated improved outcomes with the use of post-alloHCT remission therapies, prospective randomized trials are required to determine their clinical efficacy and role in the treatment of AML. On behalf of the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation, we summarize the available evidence on the use and efficacy of available pharmacologic post-remission therapies, including hypomethylating agents, deacetylase inhibitors, and tyrosine kinase inhibitors, as well as cellular therapies, including preemptive and prophylactic donor lymphocyte infusions for the prevention of relapse of AML.

摘要

急性髓系白血病(AML)是一种侵袭性血液系统恶性肿瘤,通常预后较差。异基因造血细胞移植(alloHCT)仍然是治疗中高危 AML 成人患者最有效的抗白血病治疗方法。然而,alloHCT 后疾病复发仍然不可接受地高,是 alloHCT 后治疗失败和死亡的主要原因。因此,人们对移植后早期细胞或药物维持或抢先策略以增强移植物抗白血病效应或根除持续的微小残留疾病重新产生了兴趣,特别是随着更敏感的技术来测量残留 AML 的可用性。尽管初步研究表明使用 alloHCT 缓解后治疗可改善结局,但需要前瞻性随机试验来确定其在 AML 治疗中的临床疗效和作用。代表欧洲血液和骨髓移植学会急性白血病工作组,我们总结了关于现有药物缓解后治疗的使用和疗效的可用证据,包括低甲基化剂、去乙酰化酶抑制剂和酪氨酸激酶抑制剂,以及细胞治疗,包括抢先和预防性供体淋巴细胞输注,以预防 AML 复发。

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