Long-term Exposure to Testosterone Therapy and the Risk of High Grade Prostate Cancer

J Urol. 2015 Dec;194(6):1612-6. doi: 10.1016/j.juro.2015.05.099. Epub 2015 Jun 9.

Abstract

Purpose: To our knowledge no population based studies have been done to examine whether long-term exposure to testosterone therapy is associated with an increased risk of high grade prostate cancer. We examined whether exposure to testosterone during a 5-year period was associated with an increased risk of high grade prostate cancer and whether this risk increased in a dose-response fashion with the cumulative number of testosterone injections.

Materials and methods: Using SEER (Surveillance, Epidemiology and End Results)-Medicare linked data we identified 52,579 men diagnosed with incident prostate cancer between January 1, 2001 and December 31, 2006 who had a minimum of 5 years continuous enrollment in Medicare before the cancer diagnosis. We excluded patients diagnosed at death or after autopsy, those enrolled in a health maintenance organization in the 60 months before diagnosis and those with unknown tumor grade or tumor stage. In the 5 years before diagnosis 574 men had a history of testosterone use and 51,945 did not.

Results: On logistic regression adjusting for demographic and clinical characteristics exposure to testosterone therapy was not associated with an increased risk of high grade prostate cancer (OR 0.84, 95% CI 0.67-1.05) or receipt of primary androgen deprivation therapy following diagnosis (OR 0.97, 95% CI 0.74-1.30). In addition the risk of high grade disease did not increase according to the total number of testosterone injections (OR 1.00, 95% CI 0.98-1.01).

Conclusions: Our finding that testosterone therapy was not associated with an increased risk of high grade prostate cancer may provide important information regarding the risk-benefit assessment for men with testosterone deficiency considering treatment.

Keywords: SEER program; androgens; neoplasm grade; prostatic neoplasms; testosterone.

MeSH terms

  • Aged
  • Dose-Response Relationship, Drug
  • Hormone Replacement Therapy / adverse effects*
  • Humans
  • Logistic Models
  • Long-Term Care
  • Male
  • Neoplasm Grading
  • Prostatic Neoplasms / chemically induced*
  • Prostatic Neoplasms / pathology*
  • Risk Assessment
  • SEER Program
  • Testosterone / administration & dosage
  • Testosterone / adverse effects
  • Testosterone / analogs & derivatives*
  • United States

Substances

  • Testosterone
  • testosterone 17 beta-cypionate