The emerging role of measurable residual disease detection in AML in morphologic remission

被引:27
作者
Buccisano, F. [1 ]
Maurillo, L. [1 ]
Schuurhuis, G. J. [2 ]
Del Principe, M., I [1 ]
Di Veroli, A. [1 ]
Gurnari, C. [1 ]
Venditti, A. [1 ]
机构
[1] Univ Tor Vergata Rome, Hematol Unit, Dept Biomed & Prevent, Rome, Italy
[2] Vrije Univ Amsterdam Med Ctr, Dept Hematol, Canc Ctr Amsterdam, Amsterdam, Netherlands
关键词
Minimal Measurable Disease; Acute Myeloyd Leukemia; Multiparametric Flow Cytometri; RT-qPCR; Biomarkers; Risk-adapted therapy; ACUTE MYELOID-LEUKEMIA; STEM-CELL TRANSPLANTATION; TIME QUANTITATIVE PCR; PERIPHERAL-BLOOD; RISK STRATIFICATION; PROGNOSTIC VALUE; FLOW-CYTOMETRY; DIAGNOSIS; RELAPSE; MRD;
D O I
10.1053/j.seminhematol.2018.09.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite the increasing knowledge of the genomic landscape of acute myeloid leukemia (AML), prediction merely based on genetics fails to anticipate outcome, presumably due to the heterogeneous composition of the leukemic clone determining complex interactions between different genetic abnormalities. Therefore, the introduction of a post-treatment biomarker exploring the quality of response to therapy such as assessment of measurable (previously minimal) residual disease (MRD) may lead to refinements of the prognostic assessment in AML. In this view, the European LeukemiaNet has recently endorsed the achievement of a MRD negative morphologic complete remission as a purpose the treatment. Techniques like multiparametric flow cytometry and reverse transcriptase-quantitative polymerase chain reaction have reached a level of sensitivity and specificity that make them ready for introduction in clinical practice. In the present review, we will give an update on the efforts in harmonization and/or standardization of MRD assessment in AML, focusing on the newest acquisitions in the clinical applications of MRD, and considering issues like relationship of MRD with leukemic stem cells or MRD assessment in peripheral blood. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:125 / 130
页数:6
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