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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

机译:预防预防后异种造血细胞移植治疗高风险急性髓性白血病的后期策略:专家审查欧洲血液和骨髓移植社会急性白血病工作组

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摘要

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.
机译:急性髓性白血病(AML)是一种侵略性的造血恶性肿瘤,通常与预后差有关。同种异体造血细胞移植(AllOhct)仍然是中间体和高风险AML的成人患者最有效的抗白血病治疗方法。然而,疾病复发后allOhct后仍然不可接受,并且是allohct后治疗失败和死亡率的主要原因。因此,移植后早期细胞或药物维持或先发制人的策略,以增强移植物与白血病效应或根除持续最小的残留疾病的患者已经重新兴趣,特别是在可获得更敏感的技术来测量残留的AML。虽然初步研究已经证明了使用后allohct缓解疗法的改善结果,但需要预期的随机试验来确定其临床疗效和在治疗AML的作用。代表欧洲血和骨髓移植社会的急性白血病工作组,我们总结了可用药理学后疗法使用和功效的可用证据,包括低甲基化试剂,脱乙酰酶抑制剂和酪氨酸激酶抑制剂作为细胞疗法,包括用于预防AML复发的先发型和预防性供体淋巴细胞输注。

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