Modest effect of p53, EGFR and HER-2/neu on prognosis in epithelial ovarian cancer: a meta-analysis

被引:92
作者
de Graeff, P. [3 ]
Crijns, A. P. G. [3 ]
de Jong, S. [2 ]
Boezen, M. [1 ]
Post, W. J. [1 ]
de Vries, E. G. E. [2 ]
van der Zee, A. G. J. [3 ]
de Bock, G. H. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, NL-9713 GZ Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Med Oncol, NL-9713 GZ Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Gynaecol Oncol, NL-9713 GZ Groningen, Netherlands
关键词
p53; EGFR; HER-2/neu; ovarian cancer; meta-analysis; EPIDERMAL-GROWTH-FACTOR; FACTOR RECEPTOR EXPRESSION; TUMOR-SUPPRESSOR GENE; PROTEIN EXPRESSION; POOR-PROGNOSIS; EARLY-STAGE; C-MYC; IMMUNOHISTOCHEMICAL EXPRESSION; MULTIVARIATE-ANALYSIS; CLINICAL-SIGNIFICANCE;
D O I
10.1038/sj.bjc.6605112
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: P53, EGFR and HER-2/neu are the most frequently studied molecular biological parameters in epithelial ovarian cancer, but their prognostic impact is still unequivocal. We performed a meta-analysis to more precisely estimate their prognostic significance. METHODS: Published studies that investigated the association between p53, EGFR and HER-2/neu status and survival were identified. Meta-analysis was performed using a DerSimonian-Laird model. Publication bias was investigated using funnel plots and sources of heterogeneity were identified using meta-regression analysis. RESULTS: A total of 62 studies were included for p53, 15 for EGFR and 20 for HER-2/neu. P53, EGFR and HER-2/neu status had a modest effect on overall survival (pooled HR 1.47, 95% CI 1.33-1.61 for p53; HR 1.65, 95% CI 1.25-2.19 for EGFR and HR 1.67, 95% CI 1.34-2.08 for HER-2/neu). Meta-regression analysis for p53 showed that FIGO stage distribution influenced study outcome. For EGFR and HER-2/neu, considerable publication bias was present. CONCLUSIONS: Although p53, EGFR and HER-2/neu status modestly influences survival, these markers are, by themselves, unlikely to be useful as prognostic markers in clinical practice. Our study highlights the need for well-defined, prospective clinical trials and more complete reporting of results of prognostic factor studies. British Journal of Cancer ( 2009) 101, 149-159. doi: 10.1038/sj.bjc.6605112 www.bjcancer.com Published online 9 June 2009 (C) 2009 Cancer Research UK
引用
收藏
页码:149 / 159
页数:11
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