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Updated: May 17, 2026

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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Landmarks in hormonal therapy for prostate cancer
Peter Hammerer1, Stephan Madersbacher
1Department of Urology, Academic Hospital Braunschweig, Vienna, Austria. p.hammerer@klinikumbraunschweig.de
BJU International
|October 11, 2012
Summary
Androgen-deprivation therapy (ADT) is standard for advanced prostate cancer, with luteinizing hormone-releasing hormone (LHRH) agonists widely used. New agents are needed as castration-resistant disease is inevitable.
Area of Science:
- Oncology
- Urology
- Endocrinology
Background:
- Prostate cancer is the most common cancer in men.
- Androgen deprivation therapy (ADT) has been the standard of care for over 70 years.
- Luteinizing hormone-releasing hormone (LHRH) agonists are the primary form of ADT due to extensive evidence.
Purpose of the Study:
- To review the evolution and current status of ADT in prostate cancer management.
- To highlight the importance of personalized treatment strategies.
- To emphasize the ongoing need for novel therapeutic agents.
Main Methods:
- Review of historical data and clinical trial evidence.
- Analysis of treatment guidelines and therapeutic progress.
- Discussion of current ADT modalities and future directions.
Main Results:
- ADT remains the cornerstone for non-localized prostate cancer.
- LHRH agonists are the established standard of care for ADT.
- Individualized treatment approaches are crucial for optimal outcomes.
Conclusions:
- Despite advances, ADT is essential for prostate cancer treatment.
- The development of castration-resistant prostate cancer necessitates new therapeutic agents.
- Continued research into novel ADT agents is critical for improving patient survival and quality of life.
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