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Efficacy of Testosterone Suppression with Sustained-Release Triptorelin in Advanced Prostate Cancer
Jürgen Breul1, Eija Lundström2, Daniela Purcea3
1Loretto Hospital, Freiburg, Germany.
Advances in Therapy
|December 29, 2016
Summary
Sustained-release triptorelin effectively suppresses testosterone in advanced prostate cancer (PC) patients. This androgen deprivation therapy (ADT) formulation achieves levels below 20 ng/dl, potentially offering greater clinical benefit.
Area of Science:
- Oncology
- Endocrinology
- Pharmacology
Background:
- Androgen deprivation therapy (ADT) is a standard treatment for advanced prostate cancer (PC).
- Current ADT aims for testosterone suppression below 50 ng/dl, but lower levels may improve outcomes.
- Triptorelin, a gonadotropin-releasing hormone (GnRH) agonist, is used in ADT.
Purpose of the Study:
- To evaluate the efficacy of 1-, 3-, and 6-month sustained-release (SR) triptorelin formulations.
- To assess the ability of triptorelin SR to suppress serum testosterone concentrations below 20 ng/dl.
- To analyze success rates of testosterone suppression across different triptorelin SR formulations.
Main Methods:
- Pooled retrospective analysis of 920 male PC patients from 9 prospective studies.
- Patients received triptorelin SR formulations for 2-12 months.
- Primary endpoint: serum testosterone concentration, with a target threshold of <20 ng/dl.
Main Results:
- After 1, 3, 6, 9, and 12 months, 79%, 92%, 93%, 90%, and 91% of patients achieved testosterone <20 ng/dl.
- Success rates for 1-, 3-, and 6-month formulations ranged from 80-92%, 83-93%, and 65-97%, respectively.
- Median testosterone levels at study end were 2.9, 5.0, and 8.7 ng/dl for 1-, 3-, and 6-month formulations.
Conclusions:
- Triptorelin SR formulations effectively suppress serum testosterone to <20 ng/dl in most PC patients.
- Routine monitoring of testosterone levels in PC patients on ADT is recommended.
- Further research is needed to determine the clinical benefits of very low testosterone levels.
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