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Published on: March 6, 2018
Persistent Testosterone Suppression After Cessation of Androgen Deprivation Therapy for Prostate Cancer
Jessica Delgado1, Jesse Ory2, Justin Loloi3
1Urology, University of Miami, Miami, USA.
Abstract:
Introduction Many men receiving temporary androgen deprivation therapy (ADT) for localized prostate cancer fail to achieve baseline testosterone levels after cessation. Testosterone recovery in men with localized prostate cancer receiving temporary ADT was assessed. Methods A global federated health research network (TriNetX) was used to identify men diagnosed with prostate cancer undergoing temporary ADT. Two cohorts were identified: men receiving luteinizing hormone-releasing hormone (LHRH) antagonists or LHRH agonists, and men receiving combined ADT (LHRH agonist and antiandrogens). Further stratification was based on a treatment duration of six months (short-term) or 18 months (long-term) to compare testosterone (T) recovery profiles five years after ADT cessation. Results A total of 28,583 men received LHRH agonist or antagonist therapy alone, and 20,188 men received combination ADT. A total of 46.7% of men who received short-term LHRH agonists or antagonists and 40.6% of men who received short-term combined ADT, recovered to mean baseline T levels at five years. Only men who received short-term LHRH agonists/antagonists recovered to eugonadal levels at the five-year follow-up. Around 50% of men who received long-term LHRH agonist/antagonist therapy and 10.7% of men who received combined ADT, recovered to mean baseline T levels at five years. However, neither group recovered to eugonadal T levels. Conclusions At the five-year follow-up after ADT cessation, most patients failed to recover to their mean baseline and eugonadal T levels. Given that testosterone deficiency is associated with metabolically adverse changes in body composition, increased insulin resistance, impaired bone health, and hypogonadal symptoms, serum T levels must be closely monitored in men receiving ADT following treatment cessation.
Insights
Most men do not recover baseline testosterone after temporary androgen deprivation therapy (ADT). Short-term LHRH antagonist/agonist therapy showed better testosterone recovery than combined ADT, but full eugonadal levels were rarely achieved.
Area of Science:
- Oncology
- Endocrinology
- Men's Health
Background:
- Androgen deprivation therapy (ADT) is used for localized prostate cancer.
- Testosterone recovery after temporary ADT cessation is often incomplete.
- Understanding recovery profiles is crucial for managing long-term health effects.
Purpose of the Study:
- To assess testosterone recovery in men with prostate cancer after temporary ADT.
- To compare recovery based on ADT type (LHRH antagonists/agonists vs. combined ADT) and duration (short-term vs. long-term).
Main Methods:
- Utilized the TriNetX global federated health research network.
- Identified cohorts receiving LHRH antagonists/agonists or combined ADT.
- Stratified by treatment duration (6 vs. 18 months) and analyzed testosterone levels 5 years post-cessation.
Main Results:
- 46.7% of short-term LHRH antagonist/agonist users and 40.6% of short-term combined ADT users recovered baseline testosterone.
- Only short-term LHRH antagonist/agonist users achieved eugonadal levels at 5 years.
- 50% of long-term LHRH antagonist/agonist users and 10.7% of long-term combined ADT users recovered baseline testosterone, but not eugonadal levels.
Conclusions:
- Most men fail to achieve mean baseline or eugonadal testosterone levels 5 years after temporary ADT cessation.
- Testosterone deficiency post-ADT is linked to adverse metabolic, bone, and hypogonadal symptoms.
- Close monitoring of serum testosterone levels after ADT cessation is recommended.
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