A new automated flow cytometry data analysis approach for the diagnostic screening of neoplastic B-cell disorders in peripheral blood samples with absolute lymphocytosis

被引:32
作者
Costa, E. S.
Arroyo, M. E.
Pedreira, C. E.
Garcia-Marcos, M. A.
Tabernero, M. D.
Almeida, J.
Orfao, A.
机构
[1] Univ Fed Rio de Janeiro, Inst Pediat & Puericultura Martagao Gesteira, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Dept Clin Med, Rio De Janeiro, Brazil
[3] Univ Salamanca, Cytometry Serv, Dept Med, E-37008 Salamanca, Spain
[4] Univ Salamanca, Ctr Canc Res, E-37008 Salamanca, Spain
[5] Univ Fed Rio de Janeiro, Fac Med, Rio De Janeiro, Brazil
[6] Univ Fed Rio de Janeiro, COPPE, Engn Grad Program, Rio De Janeiro, Brazil
[7] Univ Hosp Salamanca, Hematol Serv, Salamanca, Spain
[8] Univ Hosp Salamanca, Res Unity, Salamanca, Spain
关键词
lymphocytosis; B-cell chronic lymphoproliferative disorders; automated data analysis; vector quantization; pattern classification; flow cytometry;
D O I
10.1038/sj.leu.2404241
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Currently, multiparameter flow cytometry immunophenotyping is the selected method for the differential diagnostic screening between reactive lymphocytosis and neoplastic B-cell chronic lymphoproliferative disorders (B-CLPD). Despite this, current multiparameter flow cytometry data analysis approaches still remain subjective due to the need of experienced personnel for both data analysis and interpretation of the results. In this study, we describe and validate a new automated method based on vector quantization algorithms to analyze multiparameter flow cytometry immunophenotyping data in a series of 307 peripheral blood (PB) samples. Our results show that the automated method of analysis proposed compares well with currently used manual approach and significantly improves semiautomated approaches and, that by using it, a highly efficient discrimination with 100% specificity and 100% sensitivity can be made between normal/ reactive PB samples and cases with B-CLPD based on the total B-cell number and/ or the slg kappa+/slgk lambda B-cell ratio. In addition, the method proved to be able to detect the presence of pathologic neoplastic B-cells even when these are present at low frequencies (< 5% of all lymphocytes in the sample) and in poor-quality samples enriched in 'noise' events.
引用
收藏
页码:1221 / 1230
页数:10
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