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Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer
The treatment of cancer is becoming more precise, targeting specific oncogenic drivers with targeted molecular therapies. The epidermal growth factor receptor has been found to be over-expressed in a multitude of solid tumours. Immunohistochemistry is widely used in the fields of diagnostic and pers...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492076/ https://www.ncbi.nlm.nih.gov/pubmed/26149458 http://dx.doi.org/10.1186/s12967-015-0531-z |
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author | Hutchinson, Ryan A Adams, Richard A McArt, Darragh G Salto-Tellez, Manuel Jasani, Bharat Hamilton, Peter W |
author_facet | Hutchinson, Ryan A Adams, Richard A McArt, Darragh G Salto-Tellez, Manuel Jasani, Bharat Hamilton, Peter W |
author_sort | Hutchinson, Ryan A |
collection | PubMed |
description | The treatment of cancer is becoming more precise, targeting specific oncogenic drivers with targeted molecular therapies. The epidermal growth factor receptor has been found to be over-expressed in a multitude of solid tumours. Immunohistochemistry is widely used in the fields of diagnostic and personalised medicine to localise and visualise disease specific proteins. To date the clinical utility of epidermal growth factor receptor immunohistochemistry in determining monoclonal antibody efficacy has remained somewhat inconclusive. The lack of an agreed reproducible scoring criteria for epidermal growth factor receptor immunohistochemistry has, in various clinical trials yielded conflicting results as to the use of epidermal growth factor receptor immunohistochemistry assay as a companion diagnostic. This has resulted in this test being removed from the licence for the drug panitumumab and not performed in clinical practice for cetuximab. In this review we explore the reasons behind this with a particular emphasis on colorectal cancer, and to suggest a way of resolving the situation through improving the precision of epidermal growth factor receptor immunohistochemistry with quantitative image analysis of digitised images complemented with companion molecular morphological techniques such as in situ hybridisation and section based gene mutation analysis. |
format | Online Article Text |
id | pubmed-4492076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44920762015-07-07 Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer Hutchinson, Ryan A Adams, Richard A McArt, Darragh G Salto-Tellez, Manuel Jasani, Bharat Hamilton, Peter W J Transl Med Review The treatment of cancer is becoming more precise, targeting specific oncogenic drivers with targeted molecular therapies. The epidermal growth factor receptor has been found to be over-expressed in a multitude of solid tumours. Immunohistochemistry is widely used in the fields of diagnostic and personalised medicine to localise and visualise disease specific proteins. To date the clinical utility of epidermal growth factor receptor immunohistochemistry in determining monoclonal antibody efficacy has remained somewhat inconclusive. The lack of an agreed reproducible scoring criteria for epidermal growth factor receptor immunohistochemistry has, in various clinical trials yielded conflicting results as to the use of epidermal growth factor receptor immunohistochemistry assay as a companion diagnostic. This has resulted in this test being removed from the licence for the drug panitumumab and not performed in clinical practice for cetuximab. In this review we explore the reasons behind this with a particular emphasis on colorectal cancer, and to suggest a way of resolving the situation through improving the precision of epidermal growth factor receptor immunohistochemistry with quantitative image analysis of digitised images complemented with companion molecular morphological techniques such as in situ hybridisation and section based gene mutation analysis. BioMed Central 2015-07-07 /pmc/articles/PMC4492076/ /pubmed/26149458 http://dx.doi.org/10.1186/s12967-015-0531-z Text en © Hutchinson et al. 2015 This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Hutchinson, Ryan A Adams, Richard A McArt, Darragh G Salto-Tellez, Manuel Jasani, Bharat Hamilton, Peter W Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer |
title | Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer |
title_full | Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer |
title_fullStr | Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer |
title_full_unstemmed | Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer |
title_short | Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer |
title_sort | epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492076/ https://www.ncbi.nlm.nih.gov/pubmed/26149458 http://dx.doi.org/10.1186/s12967-015-0531-z |
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