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Impact of KRAS Mutations on Management of Colorectal Carcinoma

The epidermal growth factor receptor (EGFR) pathway is a therapeutic target in the management of colorectal cancer (CRC). EGFR antagonists are active in this disease; however, only a subset of patients respond to such therapy. A Kirsten ras sarcoma viral oncogene (KRAS) wild-type (WT) status of the...

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Autores principales: Sullivan, Kevin M., Kozuch, Peter S.
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062096/
https://www.ncbi.nlm.nih.gov/pubmed/21437184
http://dx.doi.org/10.4061/2011/219309
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author Sullivan, Kevin M.
Kozuch, Peter S.
author_facet Sullivan, Kevin M.
Kozuch, Peter S.
author_sort Sullivan, Kevin M.
collection PubMed
description The epidermal growth factor receptor (EGFR) pathway is a therapeutic target in the management of colorectal cancer (CRC). EGFR antagonists are active in this disease; however, only a subset of patients respond to such therapy. A Kirsten ras sarcoma viral oncogene (KRAS) wild-type (WT) status of the tumor is necessary, but possibly not sufficient, for a response to anti-EGFR monoclonal antibody therapy. Mechanisms of primary resistance to such therapy in patients harboring KRAS WT tumors are discussed. Strategies to overcome resistance to anti-EGFR monoclonal antibody therapy, including novel agents and combinations of novel therapies, are explored. Also, the use of anti-EGFR monoclonal antibodies in the adjuvant and neoadjuvant setting is reviewed.
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spelling pubmed-30620962011-03-24 Impact of KRAS Mutations on Management of Colorectal Carcinoma Sullivan, Kevin M. Kozuch, Peter S. Patholog Res Int Review Article The epidermal growth factor receptor (EGFR) pathway is a therapeutic target in the management of colorectal cancer (CRC). EGFR antagonists are active in this disease; however, only a subset of patients respond to such therapy. A Kirsten ras sarcoma viral oncogene (KRAS) wild-type (WT) status of the tumor is necessary, but possibly not sufficient, for a response to anti-EGFR monoclonal antibody therapy. Mechanisms of primary resistance to such therapy in patients harboring KRAS WT tumors are discussed. Strategies to overcome resistance to anti-EGFR monoclonal antibody therapy, including novel agents and combinations of novel therapies, are explored. Also, the use of anti-EGFR monoclonal antibodies in the adjuvant and neoadjuvant setting is reviewed. SAGE-Hindawi Access to Research 2011-03-15 /pmc/articles/PMC3062096/ /pubmed/21437184 http://dx.doi.org/10.4061/2011/219309 Text en Copyright © 2011 K. M. Sullivan and P. S. Kozuch. 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
Sullivan, Kevin M.
Kozuch, Peter S.
Impact of KRAS Mutations on Management of Colorectal Carcinoma
title Impact of KRAS Mutations on Management of Colorectal Carcinoma
title_full Impact of KRAS Mutations on Management of Colorectal Carcinoma
title_fullStr Impact of KRAS Mutations on Management of Colorectal Carcinoma
title_full_unstemmed Impact of KRAS Mutations on Management of Colorectal Carcinoma
title_short Impact of KRAS Mutations on Management of Colorectal Carcinoma
title_sort impact of kras mutations on management of colorectal carcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062096/
https://www.ncbi.nlm.nih.gov/pubmed/21437184
http://dx.doi.org/10.4061/2011/219309
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