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.
机构:
Univ Paris 05, Sorbonne Paris Cite, France
INSERM, UMR S775, F-75654 Paris 13, France
Hop Europeen Georges Pompidou, AP HP, Paris, FranceUniv Paris 05, Sorbonne Paris Cite, France
Laurent-Puig, Pierre
Manceau, Gilles
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Univ Paris 05, Sorbonne Paris Cite, France
INSERM, UMR S775, F-75654 Paris 13, FranceUniv Paris 05, Sorbonne Paris Cite, France
Manceau, Gilles
Zucman-Rossi, Jessica
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Univ Paris 05, Sorbonne Paris Cite, France
Hop Europeen Georges Pompidou, AP HP, Paris, France
INSERM, UMR S674, F-75654 Paris 13, FranceUniv Paris 05, Sorbonne Paris Cite, France
Zucman-Rossi, Jessica
Blons, Helene
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INSERM, UMR S775, F-75654 Paris 13, France
Hop Europeen Georges Pompidou, AP HP, Paris, FranceUniv Paris 05, Sorbonne Paris Cite, France
机构:
Oncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, SpainOncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain
M Ponz-Sarvisé
J Rodríguez
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Oncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, SpainOncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain
J Rodríguez
A Viudez
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机构:
Oncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, SpainOncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain
A Viudez
A Chopitea
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机构:
Oncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, SpainOncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain
A Chopitea
A Calvo
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Division of Oncology, CIMA, SpainOncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain
A Calvo
J García-Foncillas
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Oncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain Division of Oncology, CIMA, SpainOncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain
J García-Foncillas
I Gil-Bazo
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机构:
Oncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain Division of Oncology, CIMA, SpainOncology Department, Clínica Universitaria, Universidad de Navarra, Pamplona 31008, Spain
机构:
Univ Texas MD Anderson Canc Ctr, BCOP, Div Pharm, Unit 377, Houston, TX 77030 USAUniv Texas MD Anderson Canc Ctr, BCOP, Div Pharm, Unit 377, Houston, TX 77030 USA