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Pathological and Prognostic Impacts of FGFR2 Overexpression in Gastric Cancer: A Meta-Analysis

Overview
Journal J Cancer
Specialty Oncology
Date 2019 Jan 22
PMID 30662521
Citations 26
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Abstract

Fibroblast growth factor receptor-2 (FGFR2) protein expression by immunohistochemistry has been reported in up to 60% of patients with gastric cancer (GC). However, the clicopathological impacts of high FGFR2 expression have not been consistent among studies. We conducted this meta-analysis to evaluate the pathological and prognostic significance of FGFR2 overexpression in patients with GC. A systematic search of the electronic databases including PubMed, PMC, EMBASE, and Google Scholar was performed. From ten studies, 4,294 patients were included in the pooled analyses of odds ratios (ORs) with 95% confidence intervals (CIs) for pathological features and hazard ratios (HRs) with 95% CIs for overall survival according to the FGFR2 expression status. Compared with tumors showing low FGFR2 expression, GCs with FGFR2 overexpression revealed deeper depth of invasion (pT3-4) (OR = 2.63, 95% CI: 1.70-4.06, p < 0.0001), higher rate of lymph node metastasis (OR = 1.87, 95% CI: 1.31-2.67, p < 0.0001), and more advanced stage (III-IV) (OR = 1.78, 95% CI: 1.07-2.96, p = 0.03). In addition, patients with FGFR2-overexpressed GC showed significantly worse survival than those with FGFR2-low tumor (HR = 1.40, 95% CI: 1.25-1.58, p < 0.00001). In conclusion, this meta-analysis indicates that FGFR2 overexpression is associated with poor pathological features and prognosis in patients with GC.

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References
1.
Yoo C, Noh S, Shin D, Choi S, Min J . Recurrence following curative resection for gastric carcinoma. Br J Surg. 2000; 87(2):236-42. DOI: 10.1046/j.1365-2168.2000.01360.x. View

2.
Lim D, Kim D, Kang M, Kim Y, Kang W, Park C . Patterns of failure in gastric carcinoma after D2 gastrectomy and chemoradiotherapy: a radiation oncologist's view. Br J Cancer. 2004; 91(1):11-7. PMC: 2364765. DOI: 10.1038/sj.bjc.6601896. View

3.
Eswarakumar V, Lax I, Schlessinger J . Cellular signaling by fibroblast growth factor receptors. Cytokine Growth Factor Rev. 2005; 16(2):139-49. DOI: 10.1016/j.cytogfr.2005.01.001. View

4.
Grose R, Dickson C . Fibroblast growth factor signaling in tumorigenesis. Cytokine Growth Factor Rev. 2005; 16(2):179-86. DOI: 10.1016/j.cytogfr.2005.01.003. View

5.
Dailey L, Ambrosetti D, Mansukhani A, Basilico C . Mechanisms underlying differential responses to FGF signaling. Cytokine Growth Factor Rev. 2005; 16(2):233-47. DOI: 10.1016/j.cytogfr.2005.01.007. View