Monitoring of minimal residual disease in acute leukemia by multiparametric flow cytometry

被引:5
|
作者
Kusenda, J. [1 ]
Fajtova, M. [1 ]
Kovarikova, A. [1 ]
机构
[1] Slovak Acad Sci, Canc Res Inst, Bratislava 83391, Slovakia
关键词
minimal residual disease; acute leukemia; multiparameter flow cytometry; prognostic factors; remission; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; HEMATOPOIETIC-CELL TRANSPLANTATION; CHILDRENS ONCOLOGY GROUP; HIGH-RISK LEUKEMIA; CLINICAL-SIGNIFICANCE; PROGNOSTIC-FACTORS; RELAPSE RISK; AIEOP-BFM; T-CELL;
D O I
10.4149/neo_2014_017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this review, we discuss methodological principles and clinical applications of minimal residual disease (MRD) assays based on multiparameter flow cytometry (MFC). The introduction of methods for MRD detection has revolutionized monitoring of treatment response in acute leukemia. Great progress has been made in the development of wide array of flow cytometric techniques for rare event detection. This advance was accompanied by increasingly greater understanding of the immunophenotypic features of leukemic and normal lymphoid cells, and of the antigenic differences that make MRD studies possible. Immunologic testing of MRD relies on "leukemia-associated" immunophenotypes which can be identified by MFC in the most of acute leukemia cases. The recent technical innovations in routine MFC (3 lasers and >= 8 colors) and the new developments in software for data analysis make this technology the most attractive for MRD diagnostics. The importance of MFC methodology will be further strengthened by the ongoing international standardization efforts. Results of MRD testing provide unique and clinically important information. The systematic application of immunologic techniques to study MRD in clinical samples has demonstrated the prognostic significance of MRD in patients, leading to the use of MRD to regulate treatment intensity in many contemporary protocols. The identification of new markers of MRD should increase the sensitivity of MRD testing by MFC and is required to widen the applicability of MRD studies.
引用
收藏
页码:119 / 127
页数:9
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