Determinants of Epstein-Barr virus-positive gastric cancer: an international pooled analysis

被引:136
|
作者
Camargo, M. C. [1 ,2 ]
Murphy, G. [1 ]
Koriyama, C. [3 ]
Pfeiffer, R. M. [1 ]
Kim, W. H. [4 ]
Herrera-Goepfert, R. [5 ]
Corvalan, A. H. [6 ]
Carrascal, E. [7 ]
Abdirad, A. [8 ]
Anwar, M. [3 ]
Hao, Z. [9 ]
Kattoor, J. [10 ]
Yoshiwara-Wakabayashi, E. [11 ]
Eizuru, Y. [12 ]
Rabkin, C. S. [1 ]
Akiba, S. [3 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, NIH, Rockville, MD 20852 USA
[2] Univ Illinois, Div Epidemiol & Biostat, Chicago, IL 60612 USA
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Ctr Chron Viral Dis, Dept Epidemiol & Prevent Med, Kagoshima 8908544, Japan
[4] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
[5] Natl Canc Inst, Dept Pathol, Mexico City 14080, DF, Mexico
[6] Pontificia Univ Catolica, Dept Hematol & Oncol, Santiago 133202, Chile
[7] Univ Valle, Cali Canc Registry, Cali, Colombia
[8] Univ Tehran Med Sci, Inst Canc, Tehran 1417613151, Iran
[9] Guangzhou Med Coll, Affiliated Hosp 2, Dept Pathol, Guagngzhou 510260, Guangdong, Peoples R China
[10] Reg Canc Ctr, Dept Pathol, Trivandrum 695011, Kerala, India
[11] Policlin Peruano Japones, Lima, Peru
[12] Kagoshima Univ, Grad Sch Med & Dent Sci, Ctr Chron Viral Dis, Div Oncogen & Persistent Viruses, Kagoshima 8908544, Japan
基金
美国国家卫生研究院;
关键词
gastric cancer; EBV; prevalence; pooled analysis; HELICOBACTER-PYLORI; CLINICOPATHOLOGICAL FEATURES; PROTEIN EXPRESSION; CLINICAL-TRIALS; CARCINOMA; METAANALYSIS; LOCATION; EBV; ADENOCARCINOMAS; HISTOLOGY;
D O I
10.1038/bjc.2011.215
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Meta-analyses of the published literature indicate that about 9% of gastric cancers contain Epstein-Barr virus (EBV), with consistent and significant differences by sex and anatomic subsite. This study aimed to identify additional determinants of EBV positivity and their joint effects. METHODS: From 15 international populations with consistent laboratory testing for EBV, we pooled individual-level data for 5081 gastric cancer cases including information on age, sex, subsite, histologic type, diagnostic stage, geographic region, and period of diagnosis. First, we combined population-specific EBV prevalence estimates using random effects meta-analysis. We then aggregated individual-level data to estimate odds ratios of EBV positivity in relation to all variables, accounting for within-population clustering. RESULTS: In unadjusted analyses, EBV positivity was significantly higher in males, young subjects, non-antral subsites, diffuse-type histology, and in studies from the Americas. Multivariable analyses confirmed significant associations with histology and region. Sex interacted with age (P = 0.003) and subsite (P = 0.002) such that male predominance decreased with age for both subsites. The positivity of EBV was not significantly associated with either stage or time period. CONCLUSION: Aggregating individual-level data provides additional information over meta-analyses. Distinguishing histologic and geographic features as well as interactions among age, sex, and subsite further support classification of EBV-associated gastric cancer as a distinct aetiologic entity. British Journal of Cancer (2011) 105, 38-43. doi: 10.1038/bjc.2011.215 www.bjcancer.com Published online 7 June 2011 (C) 2011 Cancer Research UK
引用
收藏
页码:38 / 43
页数:6
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