Diagnostic criteria for monoclonal B-cell lymphocytosis

被引:300
作者
Marti, GE
Rawstron, AC
Ghia, P
Hillmen, P
Houlston, RS
Kay, N
Schleinitz, TA
Caporaso, N
机构
[1] NIH, Flow & Image Cytometry Sect, LSCB DCGT OCTGT, CBER FDA, Bethesda, MD 20892 USA
[2] Leeds Teaching Hosp NHS Trust, Leeds Gen Infirm, Haematol Malignancy Diagnost Serv, Leeds, W Yorkshire, England
[3] Univ Turin, Dept Oncol Sci, Candiolo, TO, Italy
[4] Ist Ric & Cura Cancro, Lab Canc Immunol, Candiolo, TO, Italy
[5] Canc Res Inst, Sect Canc Genet, Sutton, Surrey, England
[6] Mayo Clin, Div Hematol, Rochester, MN USA
[7] Inst J Paoli I Calmettes, F-13009 Marseille, France
[8] NCI, Dept Med, Div Canc Epidemiol & Genet, Genet Epidemiol Branch,NIH, Bethesda, MD 20892 USA
关键词
monoclonal B-cell lymphocytosis; B cells; early detection; surrogate biomarker; familial chronic lymphocytic leukaemia;
D O I
10.1111/j.1365-2141.2005.05550.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Very low levels of circulating monoclonal B-cell subpopulations can now be detected in apparently healthy individuals using flow cytometry. We propose the term 'monoclonal B-cell lymphocytosis' (MBL) to describe this finding. The aim of this document is to provide a working definition of MBL for future clinical, epidemiological and laboratory studies. We propose that the detection of a monoclonal B-cell population by light chain restriction is sufficient to define this condition in individuals not meeting the diagnostic criteria for other B-lymphoproliferative disorders. The majority of individuals with MBL will have cells that are indistinguishable from chronic lymphocytic leukaemia (CLL). However, this blood cell clonal expansion of CD5(+) or CD5(-) B-lymphocytes is age-dependent and immunophenotypic heterogeneity is common. Longitudinal studies are required to determine whether MBL is a precursor state to CLL or other B-lymphoproliferative disease in a situation analogous to a monoclonal gammopathy of undetermined significance and myeloma. Future studies of MBL should be directed towards determining its relationship to clinical disease, particularly in individuals from families with a genetic predisposition to developing CLL.
引用
收藏
页码:325 / 332
页数:8
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