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非 M3 急性髓系白血病中基因改变作为微小残留病灶标志物的临床价值。

Clinical values of gene alterations as marker of minimal residual disease in non-M3 acute myeloid leukemia.

机构信息

Department of Hematology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, People's Republic of China.

Center for the Study of Hematological Malignancies, Nicosia, Cyprus.

出版信息

Hematology. 2021 Dec;26(1):848-859. doi: 10.1080/16078454.2021.1990503.

Abstract

Acute myeloid leukemia (AML) is a malignant disease of the hematopoietic system. Residual leukemic cells after treatment are associated with relapse. Thus, detecting minimal residual disease (MRD) is significant. Major techniques for MRD assessment include multiparameter flow cytometry (MFC), polymerase chain reaction (PCR), and next-generation sequencing (NGS). At a molecular level, AML is the consequence of collaboration of several gene alterations. Some of these gene alterations can also be used as MRD markers to evaluate the level of residual leukemic cells by PCR and NGS. However, when as MRD markers, different gene alterations have different clinical values. This paper aims to summarize the characteristics of various MRD markers, so as to better predict the clinical outcome of AML patients and guide the treatment.

摘要

急性髓系白血病(AML)是一种造血系统的恶性疾病。治疗后残留的白血病细胞与复发相关。因此,检测微小残留病(MRD)具有重要意义。MRD 评估的主要技术包括多参数流式细胞术(MFC)、聚合酶链反应(PCR)和下一代测序(NGS)。在分子水平上,AML 是几种基因改变协同作用的结果。其中一些基因改变也可以作为 MRD 标志物,通过 PCR 和 NGS 评估残留白血病细胞的水平。然而,作为 MRD 标志物时,不同的基因改变具有不同的临床价值。本文旨在总结各种 MRD 标志物的特点,以便更好地预测 AML 患者的临床结局并指导治疗。

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