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A New Technique for Treating Low-risk Prostate Cancer—Super Active Surveillance
Published on: November 7, 2025
A Framework for Treatment Decision Making at Prostate Cancer Recurrence
Jane M Lange1, Bruce J Trock2, Roman Gulati1
1Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle WA (JML, RG, RE).
Salvage therapy (ST) after prostate-specific antigen recurrence (PSA-R) can reduce metastasis risk but may overtreat some men. A new framework helps decide if ST is beneficial, especially for men with higher Gleason scores.
Area of Science:
- Urology
- Oncology
- Medical Decision Making
Background:
- Prostate cancer patients undergoing radical prostatectomy face a significant risk of prostate-specific antigen recurrence (PSA-R).
- Deciding on salvage therapy (ST) at PSA-R is challenging due to potential benefits in reducing metastasis versus risks of overtreatment and side effects.
- A novel harm-benefit framework was developed to aid shared decision-making for ST post-PSA-R.
Purpose of the Study:
- To develop and apply a quantitative harm-benefit framework for salvage therapy (ST) decisions following prostate-specific antigen recurrence (PSA-R).
- To estimate the impact of ST on metastasis risk and overtreatment rates in patients treated with radical prostatectomy.
- To inform shared decision-making between patients and physicians regarding ST after PSA-R.
Main Methods:
- Analysis of 1,045 Johns Hopkins University Hospital patients with PSA-R post-radical prostatectomy (1984-2013).
- Utilized marginal structural models to estimate metastasis risk and ST effects, accounting for selection bias based on PSA growth.
- Developed a model to predict harm-benefit tradeoffs of ST, defining benefit as reduced metastasis risk and harm as overtreatment.
Main Results:
- Salvage therapy (ST) was associated with a 0.41 adjusted hazard ratio for metastasis.
- Treating all men at PSA-R reduced metastasis risk from 43% to 23% but resulted in 31% overtreatment.
- ST for men with Gleason score >7 reduced metastasis risk from 67% to 39% with only 13% overtreatment.
Conclusions:
- A quantitative framework evaluating ST harms and benefits aids decision-making after PSA-R.
- Immediate ST may be more appropriate for specific patient subgroups identified as having an elevated risk of metastasis.
- The framework supports personalized treatment strategies balancing metastasis prevention with avoiding unnecessary overtreatment.
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