Recurrence of prostate cancer in patients receiving testosterone supplementation for hypogonadism

Am J Health Syst Pharm. 2015 Apr 1;72(7):536-41. doi: 10.2146/ajhp140128.

Abstract

Purpose: The relationship between recurrent prostate cancer risk and testosterone replacement therapy (TRT) for hypogonadal men is explored.

Summary: The medical literature was searched to identify articles evaluating the use of TRT in symptomatic hypogonadal men with a history of prostate cancer. Eight English-language articles investigating TRT use in hypogonadal men with a history of prostate cancer were analyzed. For evaluative purposes, the normal ranges used for prostate-specific antigen (PSA) and total testosterone levels were less than 4.0 ng/mL and 300-1000 ng/dL, respectively. Most trials were small and involved patients with localized prostate cancer treated with radical prostatectomy or radiotherapy, though patients with metastatic disease or a Gleason score of ≥8 were included in a few studies. TRT was administered in a variety of dosages and dosage forms for up to nine years to manage hypogonadal symptoms. Testosterone concentrations increased, as expected, after TRT, but serum PSA levels remained below 0.1 ng/mL in the majority of patients. PSA levels were found to increase in select patients with high-risk and metastatic disease, but these elevations were not accompanied by disease progression. These studies have suggested a potential benefit for TRT use in select symptomatic hypogonadal men with a history of prostate cancer. Data were limited, however, by the retrospective nature of most studies, the lack of control groups, small sample sizes, and short follow-up periods.

Conclusion: There is insufficient evidence to withhold TRT in certain populations of men with a history of prostate cancer.

Publication types

  • Review

MeSH terms

  • Adult
  • Aged
  • Humans
  • Hypogonadism / complications*
  • Hypogonadism / drug therapy
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local / chemically induced*
  • Prostatic Neoplasms / chemically induced*
  • Testosterone / adverse effects*
  • Testosterone / therapeutic use

Substances

  • Testosterone