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Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer

Human epidermal growth factor receptor (HER)2 over-expression is associated with a shortened disease-free interval and poor survival. Although the addition of trastuzumab to chemotherapy in the first-line setting has improved response rates, progression-free survival, and overall survival, response...

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Detalles Bibliográficos
Autores principales: Morrow, Phuong Khanh H, Zambrana, Francisco, Esteva, Francisco J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750101/
https://www.ncbi.nlm.nih.gov/pubmed/19664181
http://dx.doi.org/10.1186/bcr2324
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author Morrow, Phuong Khanh H
Zambrana, Francisco
Esteva, Francisco J
author_facet Morrow, Phuong Khanh H
Zambrana, Francisco
Esteva, Francisco J
author_sort Morrow, Phuong Khanh H
collection PubMed
description Human epidermal growth factor receptor (HER)2 over-expression is associated with a shortened disease-free interval and poor survival. Although the addition of trastuzumab to chemotherapy in the first-line setting has improved response rates, progression-free survival, and overall survival, response rates declined when trastuzumab was used beyond the first-line setting because of multiple mechanisms of resistance. Studies have demonstrated the clinical utility of continuing trastuzumab beyond progression, and further trials to explore this concept are ongoing. New tyrosine kinase inhibitors, monoclonal antibodies, PTEN (phosphatase and tensin homolog) pathway regulators, HER2 antibody-drug conjugates, and inhibitors of heat shock protein-90 are being evaluated to determine whether they may have a role to play in treating trastuzumab-resistant metastatic breast cancer.
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spelling pubmed-27501012010-01-15 Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer Morrow, Phuong Khanh H Zambrana, Francisco Esteva, Francisco J Breast Cancer Res Review Human epidermal growth factor receptor (HER)2 over-expression is associated with a shortened disease-free interval and poor survival. Although the addition of trastuzumab to chemotherapy in the first-line setting has improved response rates, progression-free survival, and overall survival, response rates declined when trastuzumab was used beyond the first-line setting because of multiple mechanisms of resistance. Studies have demonstrated the clinical utility of continuing trastuzumab beyond progression, and further trials to explore this concept are ongoing. New tyrosine kinase inhibitors, monoclonal antibodies, PTEN (phosphatase and tensin homolog) pathway regulators, HER2 antibody-drug conjugates, and inhibitors of heat shock protein-90 are being evaluated to determine whether they may have a role to play in treating trastuzumab-resistant metastatic breast cancer. BioMed Central 2009 2009-07-15 /pmc/articles/PMC2750101/ /pubmed/19664181 http://dx.doi.org/10.1186/bcr2324 Text en Copyright © 2009 BioMed Central Ltd
spellingShingle Review
Morrow, Phuong Khanh H
Zambrana, Francisco
Esteva, Francisco J
Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer
title Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer
title_full Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer
title_fullStr Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer
title_full_unstemmed Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer
title_short Recent advances in systemic therapy: Advances in systemic therapy for HER2-positive metastatic breast cancer
title_sort recent advances in systemic therapy: advances in systemic therapy for her2-positive metastatic breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750101/
https://www.ncbi.nlm.nih.gov/pubmed/19664181
http://dx.doi.org/10.1186/bcr2324
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