Testosterone therapy and cancer risks among men in the SEER-Medicare linked database
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 in...
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Veröffentlicht in: | British journal of cancer 2023-01, Vol.128 (1), p.48-56 |
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Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 0007-0920 1532-1827 1532-1827 |
DOI: | 10.1038/s41416-022-02019-7 |