Testosterone therapy and cancer risks among men in the SEER-Medicare linked database

被引:3
|
作者
Butler, Ebonee N. [1 ,2 ]
Zhou, Cindy Ke [3 ]
Curry, Michael [4 ]
McMenamin, Una [5 ]
Cardwell, Christopher [5 ]
Bradley, Marie C. [1 ]
Graubard, Barry, I [6 ]
Cook, Michael B. [3 ]
机构
[1] NCI, Integrat Tumor Epidemiol Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[2] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[3] NCI, Metab Epidemiol Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[4] Informat Management Serv Inc, Calverton, MD USA
[5] Queens Univ Belfast, Ctr Publ Hlth, Canc Epidemiol Res Grp, Belfast, Antrim, North Ireland
[6] NCI, Biostat Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
关键词
SEX-HORMONES; PROSTATE-CANCER; MALIGNANT-MELANOMA; ANDROGEN; ADENOCARCINOMA; HYPOGONADISM; EPIDEMIOLOGY; ASSOCIATION; REGISTRY; TRENDS;
D O I
10.1038/s41416-022-02019-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background We examined associations between two forms of testosterone therapy (TT) and risks of seven cancers among men. Methods SEER-Medicare combines cancer registry data from the Surveillance, Epidemiology, and End Results programme with Medicare claims. Our population-based case-control study included incident cancer cases diagnosed between 1992-2015: prostate (n = 130,713), lung (n = 105,466), colorectal (n = 56,433), bladder (n = 38,873), non-Hodgkin lymphoma (n = 17,854), melanoma (n = 14,241), and oesophageal (n = 9116). We selected 100,000 controls from a 5% random sample of Medicare beneficiaries and used logistic regression to estimate odds ratios (OR) and 95% confidence intervals (CI). Results TT was associated with lower risk of distant-stage prostate cancer (injection/implantation OR = 0.72, 95% CI: 0.60-0.86; topical OR = 0.50, 95% CI: 0.24-1.03). We also observed inverse associations for distant-stage colorectal cancer (injection/implantation OR = 0.75, 95% CI: 0.62-0.90; topical OR = 0.11, 95% CI: 0.05-0.24). Risks of distant-stage colorectal and prostate cancers decreased with time after initiating TT by injection/implantation. By contrast, TT was positively associated with distant-stage melanoma (injection/implantation OR = 1.70, 95% CI: 1.37-2.11). TT was not associated with bladder cancer, oesophageal cancer, lung cancer or non-Hodgkin lymphoma. Conclusion TT was inversely associated with distant-stage prostate and colorectal cancers but was positively associated with distant-stage melanoma. These observations may suggest an aetiologic role for TT or the presence of residual confounding.
引用
收藏
页码:48 / 56
页数:9
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