Principles of Minimal Residual Disease Detection for Hematopoietic Neoplasms by Flow Cytometry

被引:108
作者
Wood, Brent L. [1 ,2 ]
机构
[1] Univ Washington, Dept Lab Med & Pathol, Seattle, WA 98109 USA
[2] Seattle Canc Care Alliance, Seattle, WA USA
关键词
cytometry; leukemia; residual; minimal; monitoring; ACUTE MYELOID-LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA; RELAPSE RISK; IMMUNOPHENOTYPIC MODULATION; CLINICAL-SIGNIFICANCE; INDUCTION THERAPY; BONE-MARROW; T-CELL; CHILDHOOD; REMISSION;
D O I
10.1002/cyto.b.21239
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Flow cytometry has become an indispensible tool for the diagnosis and classification of hematopoietic neoplasms. The ability to rapidly distinguish cellular subpopulations via multiparametric assessment of quantitative differences in antigen expression on single cells and enumerate the relative sizes of the resulting subpopulations is a key feature of the technology. More recently, these capabilities have been expanded to include the identification and enumeration of rare subpopulations within complex cellular mixtures, for example, blood or bone marrow, leading to the application for post-therapeutic monitoring or minimal residual disease detection. This review will briefly present the principles to be considered in the construction and use of flow cytometric assays for minimal residual disease detection including the use of informative antibody combinations, the impact of immunophenotypic instability, enumeration, assay sensitivity, and reproducibility. (C) 2015 International Clinical Cytometry Society
引用
收藏
页码:47 / 53
页数:7
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