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Published on: May 19, 2022
Risks of Progression After Early Androgen Deprivation Therapy for Biochemical Recurrence After Radical Prostatectomy
Timothy J Daskivich1, Shannon R Stock2,3, Stirling Cummings3
1Department of Urology, Cedars-Sinai Medical Center, Los Angeles, California.
Men receiving early androgen deprivation therapy (ADT) for prostate cancer recurrence after surgery have updated survival estimates. These findings help identify high-risk patients who may benefit from intensified treatment strategies.
Area of Science:
- Urology
- Oncology
- Prostate Cancer Research
Background:
- Prognostic models for prostate cancer recurrence often use outdated data.
- Current treatment involves early androgen deprivation therapy (ADT) before metastasis.
- Updated prognostic data is needed for men receiving early ADT post-prostatectomy.
Purpose of the Study:
- To define cancer progression and mortality rates in men receiving early ADT for biochemical recurrence (BCR) after radical prostatectomy (RP).
- To provide contemporary prognostic estimates for men with BCR post-RP treated with early ADT.
Main Methods:
- Observational study of 1108 men with nonmetastatic prostate cancer receiving ADT for BCR post-RP (1988-2019).
- Utilized Fine and Gray competing risk models to assess risks of metastasis, castrate-resistant prostate cancer (CRPC), and prostate cancer-specific mortality (PCSM).
- Key predictors analyzed included pre-ADT PSA, PSA doubling time, pathologic grade group, and seminal vesicle invasion.
Main Results:
- At 15 years post-ADT, risks were: metastasis (28%), CRPC (27%), and PCSM (19%).
- Higher pre-ADT PSA, shorter PSA doubling time, higher grade group, and seminal vesicle invasion predicted increased risk.
- Predictive nomograms and tables were developed for 3-, 5-, 10-, and 15-year risks.
Conclusions:
- Contemporary prognostic estimates are more relevant for men receiving early ADT for post-RP BCR.
- These estimates can aid in identifying high-risk patients.
- Identified patients may be candidates for intensified hormonal therapy.
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