Hospital population screening reveals overrepresentation of CD5(-) monoclonal B-cell lymphocytosis and monoclonal gammopathy of undetermined significance of IgM type

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Hospital population screening reveals overrepresentation of CD5(-) monoclonal B-cell lymphocytosis and monoclonal gammopathy of undetermined significance of IgM type. / Voigtländer, Minna; Vogler, Birthe; Trepel, Martin; Panse, Jens; Jung, Roman; Bokemeyer, Carsten; Bacher, Ulrike; Binder, Mascha.

In: ANN HEMATOL, Vol. 94, No. 9, 09.2015, p. 1559-65.

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@article{6ed60988008846b5a4f1dd48d50e90de,
title = "Hospital population screening reveals overrepresentation of CD5(-) monoclonal B-cell lymphocytosis and monoclonal gammopathy of undetermined significance of IgM type",
abstract = "Monoclonal B-cell lymphocytosis (MBL) and monoclonal gammopathy of undetermined significance (MGUS) result from clonal expansions of mature B or plasma cells. Here, we set out to determine the immunophenotypic/monoclonal immunoglobulin (M protein) features and co-prevalence of MBL and MGUS in a hospital-based cohort of 1909 non-hematooncological patients. Of the evaluable cases, 3.8 % showed evidence for MBL by immunophenotyping, while 9.8 % were screened positive for M protein by immunofixation. With six concomitant cases (0.4 %), MBL and MGUS were not statistically associated. At least in two of these coincident cases, MBL and MGUS were of different clonal origin since both clones had divergent light chain restriction. CD5(-) MBL (57.1 %) and IgM+ MGUS (24.7 %) were strikingly overrepresented compared to population-based screenings and did not progress to overt lymphoma or myeloma during the observation period (mean follow-up of 117 weeks or 110 weeks, respectively). Prevalence and phenotypes suggest that a substantial proportion of incidental MBL and MGUS in hospitalized patients may be attributed to transiently expanded B-cell clones in the context of disease-related immune stimulation rather than reflecting veritable precursors of clonal B-cell malignancies.",
keywords = "Aged, Aged, 80 and over, Antigens, CD5, B-Lymphocytes, Female, Humans, Immunoglobulin M, Lymphocytosis, Male, Middle Aged, Monoclonal Gammopathy of Undetermined Significance",
author = "Minna Voigtl{\"a}nder and Birthe Vogler and Martin Trepel and Jens Panse and Roman Jung and Carsten Bokemeyer and Ulrike Bacher and Mascha Binder",
year = "2015",
month = sep,
doi = "10.1007/s00277-015-2409-9",
language = "English",
volume = "94",
pages = "1559--65",
journal = "ANN HEMATOL",
issn = "0939-5555",
publisher = "Springer",
number = "9",

}

RIS

TY - JOUR

T1 - Hospital population screening reveals overrepresentation of CD5(-) monoclonal B-cell lymphocytosis and monoclonal gammopathy of undetermined significance of IgM type

AU - Voigtländer, Minna

AU - Vogler, Birthe

AU - Trepel, Martin

AU - Panse, Jens

AU - Jung, Roman

AU - Bokemeyer, Carsten

AU - Bacher, Ulrike

AU - Binder, Mascha

PY - 2015/9

Y1 - 2015/9

N2 - Monoclonal B-cell lymphocytosis (MBL) and monoclonal gammopathy of undetermined significance (MGUS) result from clonal expansions of mature B or plasma cells. Here, we set out to determine the immunophenotypic/monoclonal immunoglobulin (M protein) features and co-prevalence of MBL and MGUS in a hospital-based cohort of 1909 non-hematooncological patients. Of the evaluable cases, 3.8 % showed evidence for MBL by immunophenotyping, while 9.8 % were screened positive for M protein by immunofixation. With six concomitant cases (0.4 %), MBL and MGUS were not statistically associated. At least in two of these coincident cases, MBL and MGUS were of different clonal origin since both clones had divergent light chain restriction. CD5(-) MBL (57.1 %) and IgM+ MGUS (24.7 %) were strikingly overrepresented compared to population-based screenings and did not progress to overt lymphoma or myeloma during the observation period (mean follow-up of 117 weeks or 110 weeks, respectively). Prevalence and phenotypes suggest that a substantial proportion of incidental MBL and MGUS in hospitalized patients may be attributed to transiently expanded B-cell clones in the context of disease-related immune stimulation rather than reflecting veritable precursors of clonal B-cell malignancies.

AB - Monoclonal B-cell lymphocytosis (MBL) and monoclonal gammopathy of undetermined significance (MGUS) result from clonal expansions of mature B or plasma cells. Here, we set out to determine the immunophenotypic/monoclonal immunoglobulin (M protein) features and co-prevalence of MBL and MGUS in a hospital-based cohort of 1909 non-hematooncological patients. Of the evaluable cases, 3.8 % showed evidence for MBL by immunophenotyping, while 9.8 % were screened positive for M protein by immunofixation. With six concomitant cases (0.4 %), MBL and MGUS were not statistically associated. At least in two of these coincident cases, MBL and MGUS were of different clonal origin since both clones had divergent light chain restriction. CD5(-) MBL (57.1 %) and IgM+ MGUS (24.7 %) were strikingly overrepresented compared to population-based screenings and did not progress to overt lymphoma or myeloma during the observation period (mean follow-up of 117 weeks or 110 weeks, respectively). Prevalence and phenotypes suggest that a substantial proportion of incidental MBL and MGUS in hospitalized patients may be attributed to transiently expanded B-cell clones in the context of disease-related immune stimulation rather than reflecting veritable precursors of clonal B-cell malignancies.

KW - Aged

KW - Aged, 80 and over

KW - Antigens, CD5

KW - B-Lymphocytes

KW - Female

KW - Humans

KW - Immunoglobulin M

KW - Lymphocytosis

KW - Male

KW - Middle Aged

KW - Monoclonal Gammopathy of Undetermined Significance

U2 - 10.1007/s00277-015-2409-9

DO - 10.1007/s00277-015-2409-9

M3 - SCORING: Journal article

C2 - 26040471

VL - 94

SP - 1559

EP - 1565

JO - ANN HEMATOL

JF - ANN HEMATOL

SN - 0939-5555

IS - 9

ER -