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HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome

PURPOSE: Apocrine carcinoma of the breast (APO) expresses HER2 in 30–50% of cases. This study explored the clinicopathological features and outcome of HER2+/APO and matched HER2+/NST cohort. METHODS: We used the SEER database to explore the cohorts. Univariate and multivariate analyses were used to...

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Autores principales: Skenderi, Faruk, Alahmad, Mohamad Alhoda Mohamad, Tahirovic, Emin, Alahmad, Yaman M., Gatalica, Zoran, Vranic, Semir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090698/
https://www.ncbi.nlm.nih.gov/pubmed/35355162
http://dx.doi.org/10.1007/s10549-022-06578-4
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author Skenderi, Faruk
Alahmad, Mohamad Alhoda Mohamad
Tahirovic, Emin
Alahmad, Yaman M.
Gatalica, Zoran
Vranic, Semir
author_facet Skenderi, Faruk
Alahmad, Mohamad Alhoda Mohamad
Tahirovic, Emin
Alahmad, Yaman M.
Gatalica, Zoran
Vranic, Semir
author_sort Skenderi, Faruk
collection PubMed
description PURPOSE: Apocrine carcinoma of the breast (APO) expresses HER2 in 30–50% of cases. This study explored the clinicopathological features and outcome of HER2+/APO and matched HER2+/NST cohort. METHODS: We used the SEER database to explore the cohorts. Univariate and multivariate analyses were used to assess the survival. Based on ER and PR [steroid receptors/SR/] and HER2 status, we divided the cohorts to match the intrinsic molecular subtypes for comparisons. RESULTS: We retrieved 259 cases of HER2+/APO. Most HER2+/APO were SR negative (65%). HER2+/APO were more prevalent in the 80+ age group (24.7% vs. 15.7%, p < 0.001). HER2+/SR−/APO had a significantly lower histological grade than the HER2+/SR−/NST (p < 0.001). Breast cancer-related deaths were more prevalent in HER2+/NST (7.8% vs. 3.9%, p = 0.019). This was particularly evident between SR− subgroups (10.4% in HER2+/SR−/NST vs. 4.2% in HER2+/SR−/APO, p = 0.008) and was reaffirmed in breast cancer-specific survival in univariate analysis (p = 0.03). Other than race and SR status, HER2+/APO subgroups did not differ in clinicopathological parameters. CONCLUSIONS: Our study confirms the rarity of the APO and reveals that SR status in APO does not affect these patients' prognosis. HER2+/APO tumors tend to have a less aggressive phenotype and a more favorable outcome despite a markedly lower ER/PR positivity.
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spelling pubmed-90906982022-05-12 HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome Skenderi, Faruk Alahmad, Mohamad Alhoda Mohamad Tahirovic, Emin Alahmad, Yaman M. Gatalica, Zoran Vranic, Semir Breast Cancer Res Treat Brief Communication PURPOSE: Apocrine carcinoma of the breast (APO) expresses HER2 in 30–50% of cases. This study explored the clinicopathological features and outcome of HER2+/APO and matched HER2+/NST cohort. METHODS: We used the SEER database to explore the cohorts. Univariate and multivariate analyses were used to assess the survival. Based on ER and PR [steroid receptors/SR/] and HER2 status, we divided the cohorts to match the intrinsic molecular subtypes for comparisons. RESULTS: We retrieved 259 cases of HER2+/APO. Most HER2+/APO were SR negative (65%). HER2+/APO were more prevalent in the 80+ age group (24.7% vs. 15.7%, p < 0.001). HER2+/SR−/APO had a significantly lower histological grade than the HER2+/SR−/NST (p < 0.001). Breast cancer-related deaths were more prevalent in HER2+/NST (7.8% vs. 3.9%, p = 0.019). This was particularly evident between SR− subgroups (10.4% in HER2+/SR−/NST vs. 4.2% in HER2+/SR−/APO, p = 0.008) and was reaffirmed in breast cancer-specific survival in univariate analysis (p = 0.03). Other than race and SR status, HER2+/APO subgroups did not differ in clinicopathological parameters. CONCLUSIONS: Our study confirms the rarity of the APO and reveals that SR status in APO does not affect these patients' prognosis. HER2+/APO tumors tend to have a less aggressive phenotype and a more favorable outcome despite a markedly lower ER/PR positivity. Springer US 2022-03-30 2022 /pmc/articles/PMC9090698/ /pubmed/35355162 http://dx.doi.org/10.1007/s10549-022-06578-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Brief Communication
Skenderi, Faruk
Alahmad, Mohamad Alhoda Mohamad
Tahirovic, Emin
Alahmad, Yaman M.
Gatalica, Zoran
Vranic, Semir
HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome
title HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome
title_full HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome
title_fullStr HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome
title_full_unstemmed HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome
title_short HER2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome
title_sort her2-positive apocrine carcinoma of the breast: a population-based analysis of treatment and outcome
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090698/
https://www.ncbi.nlm.nih.gov/pubmed/35355162
http://dx.doi.org/10.1007/s10549-022-06578-4
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