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Modeling Breast Cancer in Human Breast Tissue using a Microphysiological System
Published on: April 23, 2021
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Male Breast Cancer
Kate M Serdy1, José Pablo Leone2, David J Dabbs1
1From the Magee-Womens Hospital of University of Pittsburgh Medical Center, Pittsburgh, PA.
American Journal of Clinical Pathology
|February 8, 2017
Summary
Male breast cancer tumors show an immunohistochemistry profile similar to female breast cancers. Second malignancies impacted survival, suggesting potential germline mutations beyond BRCA2 in male breast cancer patients.
Area of Science:
- Oncology
- Pathology
Background:
- Male breast cancer is rare, and its clinicopathologic and immunohistochemical features are less understood compared to female breast cancer.
- Understanding these characteristics is crucial for accurate diagnosis, prognosis, and treatment strategies.
Purpose of the Study:
- To present a clinicopathologic study of male invasive breast cancers.
- To emphasize the tumor immunohistochemical profile in this cohort.
- To compare the findings with those of female breast cancers.
Main Methods:
- A retrospective study of 61 cases of male invasive breast cancer.
- Analysis of tumor immunohistochemical markers including GATA-binding protein 3, androgen receptor, progesterone receptor, and human epidermal growth factor receptor 2.
- Survival analysis correlating tumor stage, receptor status, and Nottingham prognostic index.
Main Results:
- The cohort's median age was 65 years.
- Tumors were predominantly estrogen receptor-positive (97%) and rarely human epidermal growth factor receptor 2-positive (10%).
- High positivity rates were observed for GATA-binding protein 3 (98%), androgen receptor (95%), and progesterone receptor (90%). The immunohistochemistry profile was similar to female breast cancers. Overall survival was 70%, with breast cancer-specific survival at 92%. 33% developed second malignancies.
Conclusions:
- The immunohistochemistry profile of male breast cancer is similar to that of female breast cancer.
- Second malignancies significantly affected overall survival in this cohort.
- The findings suggest potential germline mutations, possibly beyond BRCA2, in male breast cancer patients.
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