Population-based study of disease trajectory after radical treatment for high-risk prostate cancer
- Pär Stattin 1, Sarah Fleming 2, Xiwu Lin 3, Florence Lefresne 4, Sabine D Brookman-May 5,6, Suneel D Mundle 5, Helen Pai 7, Dina Gifkins 7, David Robinson 8, Johan Styrke 9, Hans Garmo 1
- Pär Stattin 1, Sarah Fleming 2, Xiwu Lin 3
- 1Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
- 2Janssen Global Services, Titusville, NJ, USA.
- 3Janssen Global Services, Horsham, PA, USA.
- 4Janssen Research & Development, Los Angeles, CA, USA.
- 5Janssen Research & Development, Spring House, PA, USA.
- 6Department of Urology, Ludwig-Maximilians-University, Munich, Germany.
- 7Janssen Research & Development, Raritan, NJ, USA.
- 8Department of Urology, Ryhov County Hospital, Jönköping, Sweden.
- 9Department of Surgical and Perioperative Sciences, Urology and Andrology, Umeå University, Umeå, Sweden.
- 0Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
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View abstract on PubMed
Summary
This summary is machine-generated.Men with high-risk prostate cancer treated with radical prostatectomy (RP) had a lower risk of death from prostate cancer (PCa) and all causes compared to those treated with radiotherapy (RT). Early identification of progression is crucial.
Area Of Science
- Oncology
- Urology
- Radiotherapy
- Surgical Oncology
Background
- High-risk localized or locally advanced prostate cancer (HRLPC) requires effective long-term management strategies.
- Understanding disease trajectories after radical treatment is crucial for patient outcomes.
Purpose Of The Study
- To compare long-term disease trajectories in men with HRLPC treated with radical radiotherapy (RT) or radical prostatectomy (RP).
Main Methods
- Retrospective analysis of 13,240 men diagnosed with HRLPC between 2006-2020 from the Prostate Cancer data Base Sweden (PCBaSe) 5.0.
- Competing risk analyses using cumulative incidence were performed to assess treatment trajectories and risk of death from prostate cancer (PCa) or other causes.
- Follow-up extended to June 30, 2021, with a median follow-up of 6.2 years.
Main Results
- The 10-year risk of PCa-related death was 13% after RT versus 9% after RP. Overall mortality at 10 years was 32% after RT and 19% after RP.
- The 10-year risk of requiring androgen deprivation therapy (ADT) as secondary treatment was 42% after RT and 21% after RP.
- Among men receiving ADT, the 10-year risk of PCa-related death after ADT initiation was 33% following RT and 27% following RP.
Conclusions
- Approximately 10% of men with HRLPC died from PCa within 10 years of diagnosis, regardless of primary treatment (RT or RP).
- Men requiring secondary ADT, indicating disease progression, faced a significantly higher risk of PCa-related death.
- Prompt identification and aggressive management of men at high risk of progression post-radical treatment are essential for improving survival outcomes.
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