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Triple-Negative Breast Cancer: Adjuvant Therapeutic Options

Triple-negative breast cancer (TNBC), a subtype distinguished by negative immunohistochemical assays for expression of the estrogen and progesterone receptors (ER/PR) and human epidermal growth factor receptor-2(HER2) represents 15% of all breast cancers. Patients with TNBC generally experience a mo...

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Detalles Bibliográficos
Autores principales: Gucalp, Ayca, Traina, Tiffany A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265248/
https://www.ncbi.nlm.nih.gov/pubmed/22312556
http://dx.doi.org/10.1155/2011/696208
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author Gucalp, Ayca
Traina, Tiffany A.
author_facet Gucalp, Ayca
Traina, Tiffany A.
author_sort Gucalp, Ayca
collection PubMed
description Triple-negative breast cancer (TNBC), a subtype distinguished by negative immunohistochemical assays for expression of the estrogen and progesterone receptors (ER/PR) and human epidermal growth factor receptor-2(HER2) represents 15% of all breast cancers. Patients with TNBC generally experience a more aggressive clinical course with increased risk of disease progression and poorer overall survival. Furthermore, this subtype accounts for a disproportionate number of disease-related mortality in part due to its aggressive natural history and our lack of effective targeted agents beyond conventional cytotoxic chemotherapy. In this paper, we will review the epidemiology, risk factors, prognosis, and the molecular and clinicopathologic features that distinguish TNBC from other subtypes of breast cancer. In addition, we will examine the available data for the use of cytotoxic chemotherapy in the treatment of TNBC in both the neoadjuvant and adjuvant setting and explore the ongoing development of newer targeted agents.
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spelling pubmed-32652482012-02-06 Triple-Negative Breast Cancer: Adjuvant Therapeutic Options Gucalp, Ayca Traina, Tiffany A. Chemother Res Pract Review Article Triple-negative breast cancer (TNBC), a subtype distinguished by negative immunohistochemical assays for expression of the estrogen and progesterone receptors (ER/PR) and human epidermal growth factor receptor-2(HER2) represents 15% of all breast cancers. Patients with TNBC generally experience a more aggressive clinical course with increased risk of disease progression and poorer overall survival. Furthermore, this subtype accounts for a disproportionate number of disease-related mortality in part due to its aggressive natural history and our lack of effective targeted agents beyond conventional cytotoxic chemotherapy. In this paper, we will review the epidemiology, risk factors, prognosis, and the molecular and clinicopathologic features that distinguish TNBC from other subtypes of breast cancer. In addition, we will examine the available data for the use of cytotoxic chemotherapy in the treatment of TNBC in both the neoadjuvant and adjuvant setting and explore the ongoing development of newer targeted agents. Hindawi Publishing Corporation 2011 2011-06-21 /pmc/articles/PMC3265248/ /pubmed/22312556 http://dx.doi.org/10.1155/2011/696208 Text en Copyright © 2011 A. Gucalp and T. A. Traina. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gucalp, Ayca
Traina, Tiffany A.
Triple-Negative Breast Cancer: Adjuvant Therapeutic Options
title Triple-Negative Breast Cancer: Adjuvant Therapeutic Options
title_full Triple-Negative Breast Cancer: Adjuvant Therapeutic Options
title_fullStr Triple-Negative Breast Cancer: Adjuvant Therapeutic Options
title_full_unstemmed Triple-Negative Breast Cancer: Adjuvant Therapeutic Options
title_short Triple-Negative Breast Cancer: Adjuvant Therapeutic Options
title_sort triple-negative breast cancer: adjuvant therapeutic options
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265248/
https://www.ncbi.nlm.nih.gov/pubmed/22312556
http://dx.doi.org/10.1155/2011/696208
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