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Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers

Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of...

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Detalles Bibliográficos
Autores principales: Harandi, Amir, Zaidi, Aisha S., Stocker, Abigail M., Laber, Damian A.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2677718/
https://www.ncbi.nlm.nih.gov/pubmed/19424511
http://dx.doi.org/10.1155/2009/567486
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author Harandi, Amir
Zaidi, Aisha S.
Stocker, Abigail M.
Laber, Damian A.
author_facet Harandi, Amir
Zaidi, Aisha S.
Stocker, Abigail M.
Laber, Damian A.
author_sort Harandi, Amir
collection PubMed
description Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of clinical trials in the management of solid malignancies have become available indicating the clinical efficacy of anti-EGFR monoclonal antibodies and oral small molecule tyrosine kinase inhibitors (TKIs). This review addresses frequently used EGFR inhibitors, summarizes clinical efficacy data of these new therapeutic agents, and discusses their associated toxicity and management.
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spelling pubmed-26777182009-05-07 Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers Harandi, Amir Zaidi, Aisha S. Stocker, Abigail M. Laber, Damian A. J Oncol Review Article Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of clinical trials in the management of solid malignancies have become available indicating the clinical efficacy of anti-EGFR monoclonal antibodies and oral small molecule tyrosine kinase inhibitors (TKIs). This review addresses frequently used EGFR inhibitors, summarizes clinical efficacy data of these new therapeutic agents, and discusses their associated toxicity and management. Hindawi Publishing Corporation 2009 2009-05-06 /pmc/articles/PMC2677718/ /pubmed/19424511 http://dx.doi.org/10.1155/2009/567486 Text en Copyright © 2009 Amir Harandi et al. 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
Harandi, Amir
Zaidi, Aisha S.
Stocker, Abigail M.
Laber, Damian A.
Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
title Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
title_full Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
title_fullStr Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
title_full_unstemmed Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
title_short Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
title_sort clinical efficacy and toxicity of anti-egfr therapy in common cancers
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2677718/
https://www.ncbi.nlm.nih.gov/pubmed/19424511
http://dx.doi.org/10.1155/2009/567486
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