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Título

Prognostic relevance of receptor tyrosine kinase expression in breast cancer: A meta-analysis

AutorSeruga, Bostjan; Amir, Eitan; Pandiella, Atanasio; Ocaña, Alberto
Palabras claveTargeted therapy
Meta-analysis
Overexpression
Prognosis
Breast cancer
Receptor tyrosine kinase
Fecha de publicación2014
EditorElsevier
CitaciónCancer Treatment Reviews 40(9): 1048-1055 (2014)
Resumen[Background]: Receptor tyrosine kinases (RTKs) may facilitate tumor progression if activated aberrantly. The prognostic impact of human epidermal growth factor receptor 2 (HER2) overexpression and effectiveness of its therapeutic targeting is well established, but the effects on prognosis of overexpression of other RTKs is unknown. Here we evaluate the association of RTK expression and survival in breast cancer. [Methods]: PubMed was searched to identify studies evaluating the association between expression of RTKs other than HER2 and survival of women with breast cancer. Published data were extracted and computed into odds ratios (OR) for death at 5 years with 95% confidence intervals (CI). Data were pooled in a meta-analysis using the Mantel-Haenszel random-effect model. For studies reporting data for more than one RTK the lowest and highest OR were used for separate analyses. [Results]: Sixteen studies comprising 11,056 patients were included in the analysis. There was an association between overexpression of RTKs and decreased 5-year OS and this was highly significant when using highest ORs from studies reporting more than one RTK (OR=2.42; 95% CI=1.92-3.06, P<0.001). Similar results were observed for 5-year BCSS. Worse OS was seen with overexpression of fibroblast growth factor receptor 2/3 (FGFR) (OR=3.81; 95% CI=1.79-8.11) and epidermal growth factor receptor (EGFR)/HER1 (OR=2.45; 95% CI=1.90-3.15). [Conclusion]: Overexpression of various RTKs is associated with poor outcomes. This data suggests the clinical evaluation of combination of agents against RTKs or relevant oncogenic nodes.
URIhttp://hdl.handle.net/10261/134654
DOI10.1016/j.ctrv.2014.08.003
Identificadoresdoi: 10.1016/j.ctrv.2014.08.003
e-issn: 1532-1967
issn: 0305-7372
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