c-Met as a Prognostic Marker in Gastric Cancer: A Systematic Review and Meta-Analysis

被引:69
作者
Yu, Shan [1 ]
Yu, Yiyi [1 ]
Zhao, Naiqing [2 ]
Cui, Jianlan [2 ]
Li, Wei [1 ]
Liu, Tianshu [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Med Oncol, Shanghai 200433, Peoples R China
[2] Fudan Univ, Dept Biostat, Shanghai 200433, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 11期
基金
中国国家自然科学基金;
关键词
HEPATOCYTE GROWTH-FACTOR; FACTOR-RECEPTOR; E-CADHERIN; POOR-PROGNOSIS; EXPRESSION; AMPLIFICATION; OVEREXPRESSION; GENE; CARCINOMAS; ACTIVATION;
D O I
10.1371/journal.pone.0079137
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: c-Met has been recognized as an important therapeutic target in gastric cancer, but the prognostic property of the c-Met status is still unclear. We aimed to characterize the prognostic effect of c-Met by systematic review and meta-analysis. Methods: We identified 15 studies assessing survival in gastric cancer by c-Met status. Effect measure of interest was hazard ratio (HR) for survival. Meta-regression was performed to estimate the relationship between HR and disease stage. Random-effects meta-analyses were used to account for heterogeneity. Results: 15 eligible studies provided outcome data stratified by c-Met status in 2210 patients. Meta-analysis of the HRs indicated a significantly poorer Os in patients with high c-Met expression (average HR=2.112, 95% CI: 1.622-2.748). Subgroup analysis showed the prognostic effect of c-Met was identical in protein-level and gene-level based methodology. The same effect was also seen in Asian and Western ethnicity subgroup analysis. Meta-regression showed HR was not associated with disease stage. Conclusions: Patients with tumors that harbor high c-Met expression are more likely to have a worse Os, with this prognostic effect independent of disease stage. c-Met status should be evaluated in clinical prognosis.
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页数:10
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