Oncotarget

Meta-Analysis:

Clinicopathological impacts of high c-Met expression in renal cell carcinoma: a meta-analysis and review

Jung Han Kim _, Bum Jun Kim and Hyeong Su Kim

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Oncotarget. 2017; 8:75478-75487. https://doi.org/10.18632/oncotarget.20796

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Abstract

Jung Han Kim1,*, Bum Jun Kim1,2,* and Hyeong Su Kim1

1Division of Hemato-Oncology, Department of Internal Medicine, Kangnam Sacred-Heart Hospital, Hallym University Medical Center, Hallym University College of Medicine, Seoul 07441, Republic of Korea

2Department of Internal Medicine, National Army Capital Hospital, The Armed Forces Medical Command, Sungnam 13574, Republic of Korea

*These authors contributed equally to this work

Correspondence to:

Jung Han Kim, email: harricil@hotmail.com, harricil@hallym.or.kr

Keywords: c-Met, renal cell carcinoma, prognosis, meta-analysis

Received: June 14, 2017     Accepted: August 21, 2017     Published: September 08, 2017

ABSTRACT

c-Met overexpression has been observed in renal cell carcinoma (RCC). However, its clinicopathological impacts remain uncertain. We performed this meta-analysis to evaluate the pathologic and prognostic impacts of high c-Met expression in patients with RCC. A systematic computerized search of the electronic databases PubMed and Embase was performed. From 12 studies, 1,724 patients with RCC were included in the meta-analysis. Compared with RCCs showing low c-Met expression, tumors with high c-Met expression showed significantly higher nuclear grade (odds ratio = 2.45 [95% CI: 1.43–4.19], P = 0.001) and pT stage (odds ratio = 2.18 [95% CI: 1.27–3.72], P = 0.005). In addition, patients with c-Met-high RCC showed significantly worse overall survival than those with c-Met-low tumor (hazard ratio = 1.32 [95% CI: 1.12–1.56], P = 0.0009). In conclusion, this meta-analysis demonstrates that high c-Met expression correlate with significantly worse pathological features and overall survival, indicating c-Met overexpression is a potential adverse prognostic marker for patients with RCC.


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