Applications and efficiency of flow cytometry for leukemia diagnostics

被引:16
作者
Del Principe, Maria Ilaria [1 ,2 ]
De Bellis, Eleonora [1 ,2 ]
Gurnari, Carmelo [1 ,2 ]
Buzzati, Elisa [1 ,2 ]
Savi, Arianna [1 ,2 ]
Consalvo, Maria Antonietta Irno [2 ]
Venditti, Adriano [1 ,2 ]
机构
[1] Univ Tor Vergata, Dipartimento Biomed & Prevenz, Cattedra Ematol, Rome, Italy
[2] Fdn Policlin Tor Vergata, Dipartimento Oncoematol, Ematol, Rome, Italy
关键词
Acute leukemia; flow cytometry; immunophenotype; diagnosis; cerebrospinal fluid; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; CENTRAL-NERVOUS-SYSTEM; ACUTE MYELOGENOUS LEUKEMIA; WORLD-HEALTH-ORGANIZATION; MINIMAL RESIDUAL DISEASE; PHENOTYPE ACUTE-LEUKEMIA; HEMATOLYMPHOID NEOPLASIA; PROGNOSTIC-SIGNIFICANCE; INDUCTION THERAPY;
D O I
10.1080/14737159.2019.1691918
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Introduction: Multiparametric flow cytometry immunophenotype (MFCI) plays a crucial role in the diagnosis of acute leukemia (AL). Through the comprehensive assessment of surface and intracellular antigens expressed by blasts, MFCI permits to distinguish myeloid or B/T lymphoid AL, or AL of ambiguous lineages. By means of MFCI, the blasts can be characterized in bone marrow, peripheral blood, and body fluids, such as cerebrospinal fluid. Area covered: This review discusses how MFCI is currently applied in the diagnostic evaluation of AL; it also focuses on 'peculiar' issues such as the role of MFCI for the diagnosis of central nervous system leukemic involvement. Expert commentary: Despite the improved knowledge about the biology of AL, MFCI remains a fundamental tool to make a prompt and accurate diagnosis. MFCI also provides prognostic information for some antigens are associated with specific cytogenetic/genetic abnormalities and, recently, it became a powerful tool to evaluate the quality and depth of response (the so called 'measurable residual disease'). Its role as an efficient detector of residual disease paved the way to the investigation of tissues other than bone marrow and peripheral blood, demonstrating that even small amounts of AL appear to have a prognostic impact and may require personalized intervention.
引用
收藏
页码:1089 / 1097
页数:9
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