Monitoring minimal residual disease in acute leukemia: Technical challenges and interpretive complexities

被引:55
|
作者
Chen, Xueyan [1 ]
Wood, Brent L. [1 ,2 ]
机构
[1] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[2] Seattle Canc Care Alliance, Seattle, WA USA
关键词
Acute leukemia; Minimal residual disease; Flow cytometry; Quantitative PCR; ACUTE MYELOID-LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; MULTIPARAMETER FLOW-CYTOMETRY; STEM-CELL TRANSPLANTATION; POLYMERASE-CHAIN-REACTION; ACUTE PROMYELOCYTIC LEUKEMIA; INDEPENDENT PROGNOSTIC-FACTOR; INTERNAL TANDEM DUPLICATION; BLOOD BLAST CLEARANCE; TIME QUANTITATIVE PCR;
D O I
10.1016/j.blre.2016.09.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Minimal residual disease (MRD) after therapy has unequivocal prognostic value in acute leukemia. Over the past 20 years, a number of techniques have evolved into routine laboratory tools to detect MRD, most notably, multiparametric flow cytometry (MFC) and quantitative polymerase chain reaction (PCR)-based molecular methods. There is growing evidence that the presence of MRD detected by MFC or molecular methods provides independent prognostic information and is associated with an increased risk of relapse and shortened survival. However, the predictive value of MRD may be affected by a lack of consensus as to the timing for assessment, the methodology used, and interlaboratory variation in test performance. Herein, we review the methodological principles of MRD assays, discuss the clinical implications of monitoring MRD for risk stratification and directing further therapy, and suggest potential areas for future investigation. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:63 / 75
页数:13
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