Minimal residual disease testing in hematologic malignancies and solid cancer

被引:24
作者
Ben Lassoued, Amin [1 ]
Nivaggioni, Vanessa [2 ]
Gabert, Jean [1 ,3 ]
机构
[1] Hop Nord Marseille, AP HM, Lab Biochim & Biol Mol, Marseille, France
[2] Hop Enfants La Timone, AP HM, Lab Hematol, Marseille, France
[3] Univ Aix Marseille 2, INSERM, U1072, UNIS,Fac Med, F-13284 Marseille 07, France
关键词
acute leukemia; chronic myeloid leukemia; circulating tumor cell; CTC; minimal residual disease; multicolor flow cytometry; RT-qPCR; standardization; ACUTE MYELOID-LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; CIRCULATING TUMOR-CELLS; ACUTE PROMYELOCYTIC LEUKEMIA; TIME QUANTITATIVE PCR; POLYMERASE-CHAIN-REACTION; INTERNAL TANDEM DUPLICATION; TYROSINE KINASE INHIBITORS; CHRONIC MYELOGENOUS LEUKEMIA; IG/TCR GENE REARRANGEMENTS;
D O I
10.1586/14737159.2014.927311
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Minimal residual disease (MRD) assays are of a great value to assess treatment efficacy and may provide prognostic information. This is particularly relevant in the era of targeted therapy where the introduction of MRD monitoring has fundamentally transformed the way in which cancer patients are managed. While MRD guidelines are well-established for chronic myeloid leukemia, acute promyelocytic leukemia and acute lymphoblastic leukemia, areas for continuing development are available. High level of standardization and regular external quality control rounds and recommendations for data interpretation remain essential to improve MRD monitoring. In this review, we describe the different applications of MRD assays in most frequent hematologic malignancies and solid cancer and provide an overview of the strengths and potential weaknesses of each method.
引用
收藏
页码:699 / 712
页数:14
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