Minimal/Measurable Residual Disease Detection in Acute Leukemias by Multiparameter Flow Cytometry

被引:18
作者
Fuda, Franklin [1 ]
Chen, Weina [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Pathol, BioCtr EB3 234, 2330 Inwood Rd, Dallas, TX 75390 USA
关键词
Acute myeloid leukemia; Lymphoblastic leukemia; Minimal residual disease detection; Measurable residual disease detection; Immunophenotype; Multiparameter flow cytometry; Real-time quantitative polymerase chain reaction; Next-generation sequencing; ACUTE MYELOID-LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; ASSAYS PRACTICE GUIDELINES; CHRONIC LYMPHOCYTIC-LEUKEMIA; CONCERTED ACTION REPORT; PERIPHERAL-BLOOD; BONE-MARROW; HIGH-RISK; INDUCTION THERAPY; STEM-CELLS;
D O I
10.1007/s11899-018-0479-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of ReviewMinimal or measurable residual disease (MRD) detected by multiparameter flow cytometry (MFC) is an independent prognostic indicator in acute leukemia. However, the predictive value of MFC MRD is affected by technical challenges, interpretive complexities, and inadequate standardization, particularly in acute myeloid leukemia (AML). Here, we critically review the methodological principles of the MFC MRD assay and discuss clinical implications of MRD.Recent FindingsKey components of MFC MRD assays to be discussed include the principles of MFC, panel selection, analysis approaches, level of quantifiable MRD and calculation, reporting, and areas of improvements. Key components of clinical implications include context-dependent detection threshold and the integral role of MRD assessment by MFC in the era of ever-expanding molecular testing.SummaryWith advancements in technology and standardization, MFC along with molecular assays will continue to play an important role in MRD assessment to evaluate treatment response and risk stratification.
引用
收藏
页码:455 / 466
页数:12
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