Division of Hematology/Oncology, Department of Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
Leuk Lymphoma. 2021 Jan;62(1):8-31. doi: 10.1080/10428194.2020.1827251. Epub 2020 Nov 2.
Allogeneic hematopoietic stem cell transplantation (alloHCT) results in improved outcomes for acute myeloid leukemia (AML) patients compared to consolidation chemotherapy in transplant-eligible patients with adverse-risk disease. Despite achieving a complete remission (CR) to initial therapy, defined as <5% bone marrow blasts with recovery of peripheral blood elements, a large number of patients suffer disease relapse following alloHCT. There is a growing focus on minimal or measurable residual disease (MRD) in patients with AML, variably defined using multiparametric flow cytometry and nucleic acid sequencing techniques, to detect levels of disease not included in current CR terminology. MRD has emerged as an important prognostic tool in AML and may improve risk stratification, further refine selection of post-remission treatment, and provide an opportunity for therapeutic intervention. Herein, we review MRD detection methods, timing of measurement, prognostic implications, and MRD-directed therapy in AML patients undergoing alloHCT.
异基因造血干细胞移植(alloHCT)可改善急性髓系白血病(AML)患者的预后,与移植适应证患者中不良风险疾病的巩固化疗相比。尽管初始治疗达到完全缓解(CR),定义为骨髓原始细胞<5%,外周血成分恢复,但大量患者在 alloHCT 后发生疾病复发。目前,人们越来越关注 AML 患者的微小残留病(MRD),采用多参数流式细胞术和核酸测序技术对其进行定义,以检测当前 CR 术语中未包括的疾病水平。MRD 已成为 AML 的重要预后工具,可改善风险分层,进一步精细选择缓解后治疗,并为治疗干预提供机会。在此,我们综述了 AML 患者 alloHCT 中 MRD 的检测方法、检测时间、预后意义以及基于 MRD 的治疗。