Prognostic value of c-MET in head and neck cancer: A systematic review and meta-analysis of aggregate data.
Details
Serval ID
serval:BIB_BFC5FC0A60D1
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Prognostic value of c-MET in head and neck cancer: A systematic review and meta-analysis of aggregate data.
Journal
Oral oncology
ISSN
1879-0593 (Electronic)
ISSN-L
1368-8375
Publication state
Published
Issued date
11/2017
Peer-reviewed
Oui
Volume
74
Pages
68-76
Language
english
Notes
Publication types: Journal Article ; Meta-Analysis ; Review ; Systematic Review
Publication Status: ppublish
Publication Status: ppublish
Abstract
The hepatocyte growth factor (HGF)/mesenchymal-epithelial transition factor (c-MET) ligand/receptor axis has been implicated in pathogenesis of malignant diseases including squamous cell carcinoma of the head and neck (SCCHN). Overexpression of c-MET has been reported as a common molecular abnormality in SCCHN, although its prognostic and predictive value remains to be validated.
We systematically searched literature for studies evaluating c-MET expression on immunohistochemistry in newly diagnosed, non-metastatic SCCHN. The c-MET expressing cases were classified into three categories according to predefined cut-off values for positivity. Our aim was to assess the prevalence of c-MET expression and its relationship with selected clinicopathological variables.
Twenty-eight studies with 2019 cases were included. Relative frequencies of c-MET expression above cut-off levels I, II, and III were 81.8%, 63.8%, and 46.2%, respectively. Differences between these three values were statistically significant (p<1.0×10 <sup>-6</sup> ). Above cut-off level II, c-MET positivity was associated with worse overall survival (p=4.0×10 <sup>-6</sup> ), positive nodal status (p=1.0×10 <sup>-4</sup> ), higher disease stage (p=7.0×10 <sup>-4</sup> ), older age (p=2.1×10 <sup>-3</sup> ), disease recurrence (p=2.0×10 <sup>-2</sup> ), and primary tumour localization in the oral cavity (p=2.3×10 <sup>-2</sup> ). Above cut-off level III, c-MET positivity was associated with worse disease-free or progression-free survival (p=9.0×10 <sup>-6</sup> ), p16 negativity (p=2.4×10 <sup>-4</sup> ), worse overall survival (p=4.0×10 <sup>-4</sup> ), positive epidermal growth factor receptor (EGFR) status (p=7.2×10 <sup>-4</sup> ), and larger primary tumours (p=4.6×10 <sup>-3</sup> ).
In SCCHN, immunohistochemical overexpression of c-MET above cut-off levels III and particularly II was associated with inferior survival outcomes and advanced disease. Moreover, it represents a promising predictive biomarker for c-MET targeting, yet the optimal scoring method remains to be defined.
We systematically searched literature for studies evaluating c-MET expression on immunohistochemistry in newly diagnosed, non-metastatic SCCHN. The c-MET expressing cases were classified into three categories according to predefined cut-off values for positivity. Our aim was to assess the prevalence of c-MET expression and its relationship with selected clinicopathological variables.
Twenty-eight studies with 2019 cases were included. Relative frequencies of c-MET expression above cut-off levels I, II, and III were 81.8%, 63.8%, and 46.2%, respectively. Differences between these three values were statistically significant (p<1.0×10 <sup>-6</sup> ). Above cut-off level II, c-MET positivity was associated with worse overall survival (p=4.0×10 <sup>-6</sup> ), positive nodal status (p=1.0×10 <sup>-4</sup> ), higher disease stage (p=7.0×10 <sup>-4</sup> ), older age (p=2.1×10 <sup>-3</sup> ), disease recurrence (p=2.0×10 <sup>-2</sup> ), and primary tumour localization in the oral cavity (p=2.3×10 <sup>-2</sup> ). Above cut-off level III, c-MET positivity was associated with worse disease-free or progression-free survival (p=9.0×10 <sup>-6</sup> ), p16 negativity (p=2.4×10 <sup>-4</sup> ), worse overall survival (p=4.0×10 <sup>-4</sup> ), positive epidermal growth factor receptor (EGFR) status (p=7.2×10 <sup>-4</sup> ), and larger primary tumours (p=4.6×10 <sup>-3</sup> ).
In SCCHN, immunohistochemical overexpression of c-MET above cut-off levels III and particularly II was associated with inferior survival outcomes and advanced disease. Moreover, it represents a promising predictive biomarker for c-MET targeting, yet the optimal scoring method remains to be defined.
Keywords
Carcinoma, Squamous Cell/genetics, Carcinoma, Squamous Cell/pathology, Carcinoma, Squamous Cell/physiopathology, Epithelial-Mesenchymal Transition, Female, Head and Neck Neoplasms/genetics, Head and Neck Neoplasms/pathology, Head and Neck Neoplasms/physiopathology, Humans, Immunohistochemistry, Male, Middle Aged, Prognosis, Proto-Oncogene Proteins c-met/genetics, Proto-Oncogene Proteins c-met/physiology, Squamous Cell Carcinoma of Head and Neck, Survival Analysis, Head and neck cancer, Overexpression, Predictive factor, Prognostic factor, c-MET receptor
Pubmed
Web of science
Create date
28/12/2024 23:38
Last modification date
29/12/2024 8:10