Estimating age-specific breast cancer risks:: a descriptive tool to identify age interactions

被引:42
作者
Anderson, William F.
Matsuno, Rayna K.
Sherman, Mark E.
Lissowska, Jolanta
Gail, Mitchell H.
Brinton, Louise A.
Yang, Xiaohong
Peplonska, Beata
Chen, Bingshu E.
Rosenberg, Philip S.
Chatterjee, Nilanjan
Szeszenia-Dabrowska, Neonila
Bardin-Mikolajczak, Alicja
Zatonski, Witold
Devesa, Susan S.
Garcia-Closas, Montserrat
机构
[1] NCI, DHHS, DCEG, Biostat Branch,EPS,NIH, Bethesda, MD 20892 USA
[2] NCI, Div Canc Epidemiol & Genet, NIH, Bethesda, MD 20892 USA
[3] Ctr Canc, Dept Canc Epidemiol & Prevent, PL-02781 Warsaw, Poland
[4] Marie Sklodowska Curie Inst Oncol, PL-02781 Warsaw, Poland
[5] Nofer Inst Occupat Med, Lodz, Poland
关键词
population-based case-control study; absolute risks; relative risks; odds ratio; rate ratios;
D O I
10.1007/s10552-006-0092-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Clarifying age-specific female breast cancer risks and interactions may provide important etiologic clues. Method: Using a population-based case-control study in Poland (2000-2003) of 2,386 incident breast cancer cases and 2,502 control subjects aged 25-74 years, we estimated age-specific breast cancer incidence rates according to risk factors. Results: Breast cancer risks were elevated among women with positive family history (FH), younger age at menarche, older age at first full-term birth, nulliparity, exogenous hormonal usage, and reduced physical activity (PA). Notwithstanding overall risks, we observed statistically significant quantitative (non-crossover) and qualitative (crossover) age interactions for all risk factors except for FH and PA. For example, nulliparity compared to parity reduced breast cancer risk among women ages 25-39 years then rates crossed or reversed, after which nulliparity increased relative risks among women ages 40-74 years. Conclusion: Though quantitative age interactions could be expected, qualitative interactions were somewhat counterintuitive. If confirmed in other populations, qualitative interactions for a continuous covariate such as age will be difficult to reconcile in a sequential (multistep or monolithic) 'stochastic' breast cancer model. Alternatively, the reversal of relative risks among younger and older women suggests subgroup heterogeneity with different etiologic mechanisms for early-onset and late-onset breast cancer types. © 2007 Springer Science+Business Media B.V.
引用
收藏
页码:439 / 447
页数:9
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