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Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer

The incidence of male breast cancer (MBC) is rising. Current treatment regimens for MBC are extrapolated from female breast cancer (FBC), based on the assumption that FBC prognostic features and therapeutic targets can be extrapolated to MBC. However, there is yet little evidence that prognostic fea...

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Autores principales: Lacle, Miangela M., van der Pol, Carmen, Witkamp, Arjen, van der Wall, Elsken, van Diest, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613416/
https://www.ncbi.nlm.nih.gov/pubmed/23573235
http://dx.doi.org/10.1371/journal.pone.0060138
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author Lacle, Miangela M.
van der Pol, Carmen
Witkamp, Arjen
van der Wall, Elsken
van Diest, Paul J.
author_facet Lacle, Miangela M.
van der Pol, Carmen
Witkamp, Arjen
van der Wall, Elsken
van Diest, Paul J.
author_sort Lacle, Miangela M.
collection PubMed
description The incidence of male breast cancer (MBC) is rising. Current treatment regimens for MBC are extrapolated from female breast cancer (FBC), based on the assumption that FBC prognostic features and therapeutic targets can be extrapolated to MBC. However, there is yet little evidence that prognostic features that have been developed and established in FBC are applicable to MBC as well. In a recent study on FBC, a combination of mitotic index and Bcl2 expression proved to be of strong prognostic value. Previous papers on Bcl2 expression in MBC were equivocal, and the prognostic value of Bcl2 combined with mitotic index has not been studied in MBC. The aim of the present study was therefore to investigate the prognostic value of Bcl2 in combination with mitotic index in MBC. Immunohistochemical staining for Bcl2 was performed on tissue microarrays of a total of 151 male breast cancer cases. Mitotic index was scored. The prognostic value of Bcl2 expression and Bcl2/mitotic index combinations was evaluated studying their correlations with clinicopathologic features and their prediction of survival. The vast majority of MBC (94%) showed Bcl2 expression, more frequently than previously described for FBC. Bcl2 expression had no significant associations with clinicopathologic features such as tumor size, mitotic count and grade. In univariate survival analysis, Bcl2 had no prognostic value, and showed no additional prognostic value to tumor size and histological grade in Cox regression. In addition, the Bcl2/mitotic index combination as opposed to FBC did not predict survival in MBC. In conclusion, Bcl2 expression is common in MBC, but is not associated with major clinicopathologic features and, in contrast to FBC, does not seem to have prognostic value, also when combined with mitotic index.
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spelling pubmed-36134162013-04-09 Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer Lacle, Miangela M. van der Pol, Carmen Witkamp, Arjen van der Wall, Elsken van Diest, Paul J. PLoS One Research Article The incidence of male breast cancer (MBC) is rising. Current treatment regimens for MBC are extrapolated from female breast cancer (FBC), based on the assumption that FBC prognostic features and therapeutic targets can be extrapolated to MBC. However, there is yet little evidence that prognostic features that have been developed and established in FBC are applicable to MBC as well. In a recent study on FBC, a combination of mitotic index and Bcl2 expression proved to be of strong prognostic value. Previous papers on Bcl2 expression in MBC were equivocal, and the prognostic value of Bcl2 combined with mitotic index has not been studied in MBC. The aim of the present study was therefore to investigate the prognostic value of Bcl2 in combination with mitotic index in MBC. Immunohistochemical staining for Bcl2 was performed on tissue microarrays of a total of 151 male breast cancer cases. Mitotic index was scored. The prognostic value of Bcl2 expression and Bcl2/mitotic index combinations was evaluated studying their correlations with clinicopathologic features and their prediction of survival. The vast majority of MBC (94%) showed Bcl2 expression, more frequently than previously described for FBC. Bcl2 expression had no significant associations with clinicopathologic features such as tumor size, mitotic count and grade. In univariate survival analysis, Bcl2 had no prognostic value, and showed no additional prognostic value to tumor size and histological grade in Cox regression. In addition, the Bcl2/mitotic index combination as opposed to FBC did not predict survival in MBC. In conclusion, Bcl2 expression is common in MBC, but is not associated with major clinicopathologic features and, in contrast to FBC, does not seem to have prognostic value, also when combined with mitotic index. Public Library of Science 2013-04-01 /pmc/articles/PMC3613416/ /pubmed/23573235 http://dx.doi.org/10.1371/journal.pone.0060138 Text en © 2013 Lacle et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lacle, Miangela M.
van der Pol, Carmen
Witkamp, Arjen
van der Wall, Elsken
van Diest, Paul J.
Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer
title Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer
title_full Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer
title_fullStr Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer
title_full_unstemmed Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer
title_short Prognostic Value of Mitotic Index and Bcl2 Expression in Male Breast Cancer
title_sort prognostic value of mitotic index and bcl2 expression in male breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613416/
https://www.ncbi.nlm.nih.gov/pubmed/23573235
http://dx.doi.org/10.1371/journal.pone.0060138
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