Epidermal growth factor receptor immunohistochemistry: new opportunities in metastatic colorectal cancer

被引:37
|
作者
Hutchinson, Ryan A. [1 ]
Adams, Richard A. [2 ]
Mcart, Darragh G. [1 ]
Salto-Tellez, Manuel [1 ]
Jasani, Bharat [3 ]
Hamilton, Peter W. [1 ]
机构
[1] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Belfast BT9 7AE, Antrim, North Ireland
[2] Cardiff Univ, Sch Med, Inst Canc & Genet, Inst Med Genet Bldg, Cardiff CF14 4XN, S Glam, Wales
[3] Nazarbayev Univ, Sch Med, Dept Biomed Sci, Astana 010000, Kazakhstan
关键词
Epidermal growth factor receptor; Immunohistochemistry; Personalised medicine; Heterogeneity; Metastatic colorectal cancer; Image analysis; Localisation; GENE COPY NUMBER; IN-SITU HYBRIDIZATION; CELL LUNG-CANCER; FOLFIRI PLUS BEVACIZUMAB; ANTI-EGFR THERAPY; PHASE-III TRIAL; BREAST-CANCER; 1ST-LINE TREATMENT; COMBINATION CHEMOTHERAPY; INTERNATIONAL KI67;
D O I
10.1186/s12967-015-0531-z
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页数:11
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