Serum testosterone is associated with aggressive prostate cancer in older men: results from the Baltimore Longitudinal Study of Aging

• Published in: BJU international Vol. 105; no. 6; pp. 824 - 829
• Main Authors: Pierorazio, Phillip M., Ferrucci, Luigi, Kettermann, Anna, Longo, Dan L., Metter, E. Jeffrey, Carter, H. Ballentine
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.03.2010; Wiley-Blackwell
• Subjects: Adult; Age Factors; Aged; Aged, 80 and over; Baltimore - epidemiology; Biological and medical sciences; Disease Progression; Epidemiologic Methods; Gynecology. Andrology. Obstetrics; high‐risk; Humans; Male; Male genital diseases; Medical sciences; Middle Aged; Nephrology. Urinary tract diseases; prostate cancer; Prostatic Neoplasms - blood; Prostatic Neoplasms - epidemiology; Prostatic Neoplasms - pathology; testosterone; Testosterone - blood; Tumors; Tumors of the urinary system; Urinary tract. Prostate gland; Baltimore; Human; High risk; Nephrology; Urinary system disease; Androgen; Prostate disease; Ageing; Male; Malignant tumor; high-risk; Urology; Testosterone; Follow up study; Adult; Serum; Testicular hormone; Sex steroid hormone; Male genital diseases; Prostate cancer; Elderly; Age; Cancer; High malignancy
• ISSN: 1464-4096; 1464-410X
• DOI: 10.1111/j.1464-410X.2009.08853.x

Study Type – Prognosis (inception cohort)
Level of Evidence 1b OBJECTIVE To evaluate the relationship between testosterone levels and the development of high‐risk prostate cancer, by prospectively examining serum androgen concentrations in a well‐studied cohort, as the role of testosterone in prostate cancer progression is debated. PATIENTS AND METHODS The study comprised 781 men in the Baltimore Longitudinal Study of Aging who had sex steroid measurements before a diagnosis of prostate cancer, or at their last visit for those without cancer (no cancer, 636; cancer, not high risk, 109; cancer, high risk, 36). High‐risk cancer was defined as death from prostate cancer, a prostate specific antigen (PSA) level of ≥20 ng/mL at diagnosis, or a Gleason score of ≥8. The hazard ratio (HR) of high‐risk disease was determined using a Cox proportional hazards regression model with simple updating, and risk rates were stratified by age and tercile for androgens of interest based on the proportional hazards analyses. RESULTS The likelihood of high‐risk prostate cancer doubled per unit (0.1) increase in the free testosterone index (FTI) for patients aged >65 years (HR 2.07, 95% confidence interval, CI, 1.01–4.23; P = 0.047); the likelihood for men aged ≤65 years was inversely related to the FTI (HR 0.96, 95% CI 0.35–2.6; P = 0.9). The risk rate per person‐years increased from lowest to highest tercile of FTI for the oldest men (age >70 years) but this trend was not apparent among younger men. CONCLUSION Higher levels of serum free testosterone are associated with an increased risk of aggressive prostate cancer among older men. These data highlight the importance of prospective trials to insure the safety of testosterone‐replacement therapy.