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Testosterone replacement therapy in men with prostate cancer: a time-varying analysis
Alan L Kaplan1, Andrew T Lenis, Adit Shah
1Department of Urology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
The Journal of Sexual Medicine
|December 16, 2014
Summary
Testosterone replacement therapy (TRT) after prostate cancer treatment is safe. Longer TRT duration did not increase mortality or the need for salvage androgen deprivation therapy (ADT).
Area of Science:
- Oncology
- Endocrinology
- Men's Health
Background:
- Testosterone replacement therapy (TRT) use in men with prostate cancer is controversial due to concerns about androgen-driven cancer progression.
- Emerging evidence suggests TRT may be safe, but dose-related effects remain uninvestigated.
Purpose of the Study:
- To determine if increasing TRT exposure is associated with adverse outcomes in men with prostate cancer using time-varying analysis.
- To investigate the relationship between TRT duration and mortality or need for salvage androgen deprivation therapy (ADT).
Main Methods:
- Utilized linked Surveillance, Epidemiology, and End Results-Medicare data for 149,354 men diagnosed with prostate cancer (1991-2007).
- Stratified men treated with TRT by treatment duration and used weighted propensity score methods for adjustment.
- Employed a Cox proportional hazards model to assess the impact of injectable TRT exposure on outcomes.
Main Results:
- TRT, irrespective of duration, was not linked to increased overall mortality (OM) or prostate cancer-specific mortality (PCSM). Hazard ratios (HR) for OM and PCSM were <1.0 (P ≤ 0.002).
- No significant difference in salvage ADT use was observed for TRT durations of ≤30 days (HR 1.23) or 31-60 days (HR 1.05) compared to no TRT.
- Long-term TRT use was associated with a lower need for salvage ADT (HR 0.70, P=0.04).
Conclusions:
- Testosterone replacement therapy following prostate cancer diagnosis and treatment does not elevate mortality rates or the requirement for salvage ADT.
- Time-varying analysis confirms that extended TRT duration is not associated with adverse mortality outcomes or increased need for ADT.
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