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Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer

Two anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (MoAbs) have been approved in Canada for the treatment of metastatic colorectal cancer (mCRC) – cetuximab, a mouse-human chimeric MoAb, and panitumumab, a fully human MoAb. This paper reviews the efficacy of the anti-EGFR monoclo...

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Detalles Bibliográficos
Autores principales: Fakih, M., Wong, R.
Formato: Texto
Lenguaje:English
Publicado: Multimed Inc. 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901794/
https://www.ncbi.nlm.nih.gov/pubmed/20680105
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author Fakih, M.
Wong, R.
author_facet Fakih, M.
Wong, R.
author_sort Fakih, M.
collection PubMed
description Two anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (MoAbs) have been approved in Canada for the treatment of metastatic colorectal cancer (mCRC) – cetuximab, a mouse-human chimeric MoAb, and panitumumab, a fully human MoAb. This paper reviews the efficacy of the anti-EGFR monoclonal antibodies cetuximab and panitumumab – both as monotherapy and in combination with cytotoxic chemotherapy – in the treatment of mCRC. Both cetuximab and panitumumab have demonstrated clinical efficacy in monotherapy in patients with mCRC, an advantage that has recently been found to be limited largely to those with wild-type KRAS tumors. Advantages of using these agents in monotherapy include reduced cost and toxicity. While the addition of cetuximab to irinotecan has shown superior progression-free survival and response compared with cetuximab monotherapy, there is currently no evidence for a benefit of panitumumab in combination with irinotecan.
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spelling pubmed-29017942010-08-02 Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer Fakih, M. Wong, R. Curr Oncol Medical Oncology Two anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (MoAbs) have been approved in Canada for the treatment of metastatic colorectal cancer (mCRC) – cetuximab, a mouse-human chimeric MoAb, and panitumumab, a fully human MoAb. This paper reviews the efficacy of the anti-EGFR monoclonal antibodies cetuximab and panitumumab – both as monotherapy and in combination with cytotoxic chemotherapy – in the treatment of mCRC. Both cetuximab and panitumumab have demonstrated clinical efficacy in monotherapy in patients with mCRC, an advantage that has recently been found to be limited largely to those with wild-type KRAS tumors. Advantages of using these agents in monotherapy include reduced cost and toxicity. While the addition of cetuximab to irinotecan has shown superior progression-free survival and response compared with cetuximab monotherapy, there is currently no evidence for a benefit of panitumumab in combination with irinotecan. Multimed Inc. 2010-07 /pmc/articles/PMC2901794/ /pubmed/20680105 Text en 2010 Multimed Inc. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Medical Oncology
Fakih, M.
Wong, R.
Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer
title Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer
title_full Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer
title_fullStr Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer
title_full_unstemmed Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer
title_short Efficacy of the monoclonal antibody EGFR inhibitors for the treatment of metastatic colorectal cancer
title_sort efficacy of the monoclonal antibody egfr inhibitors for the treatment of metastatic colorectal cancer
topic Medical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901794/
https://www.ncbi.nlm.nih.gov/pubmed/20680105
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