Abstract
Histopathological findings and molecular alterations well reflect the biological properties of individual primary breast carcinomas. Specifically, pT (size of the invasive component), pN (number of metastatic lymph nodes), histological or nuclear grade, lymphovascular invasion, hormone receptors, and HER2 (c-erbB-2) gene overexpresison or amplification are known to be effective markers for assessing the risk of operable primary breast carcinoma, albeit incompletely. It is expected that additional molecular markers and novel diagnostic tools will be developed in the future to facilitate a more accurate characterization of higher risk node-negative breast carcinomas.
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Abbreviations
- CGH:
-
Comparative genomic hybridization
- CK:
-
Cytokeratin
- DCIS:
-
Ductal carcinoma in situ
- EGFR:
-
Epidermal growth factor receptor
- ER:
-
Estrogen receptor
- HE:
-
Hematoxylin and eosin
- IHC:
-
Immunohistochemistry
- ITC:
-
Isolated tumor cells
- LCIS:
-
Lobular carcinoma in situ
- ly:
-
Lymphatic invasion
- NCCN:
-
National Comprehensive Cancer Network
- pCR:
-
Pathological complete response
- PgR:
-
Progesterone receptor
- PST:
-
Primary systemic therapies
- SLN:
-
Sentinel lymph node
- SNNS:
-
Sentinel lymph node navigation surgery
- v:
-
Vascular invasion
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Acknowledgments
This work was supported in part by a Grant-in-Aid for Cancer Research (16–6) from the Ministry of Health, Labor, and Welfare, and by a Grant-in-Aid from the Foundation for the Promotion of Defense Medicine.
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This article is based on a presentation delivered at Presidential Symposium 1, “Breast cancer: individualized diagnosis for tailored treatment,” held on 29 June 2007 at the 15th Annual Meeting of the Japanese Breast Cancer Society in Yokohama.
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Tsuda, H. Individualization of breast cancer based on histopathological features and molecular alterations. Breast Cancer 15, 121–132 (2008). https://doi.org/10.1007/s12282-008-0032-5
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DOI: https://doi.org/10.1007/s12282-008-0032-5