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Retzius-Sparing Robot-Assisted Radical Prostatectomy
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Does benign prostatic tissue contribute to measurable PSA levels after radical prostatectomy?
Guilherme Godoy1, Basir U Tareen, Herbert Lepor
1Division of Urologic Oncology, Department of Urology, New York University School of Medicine, New York, New York 10016, USA.
Urology
|May 2, 2009
Summary
For men with extremely low-risk prostate cancer, a measurable prostate-specific antigen (PSA) level after radical prostatectomy is rare. Benign prostatic tissue is an unlikely source of elevated PSA post-surgery.
Area of Science:
- Urology
- Oncology
Background:
- Prostate-specific antigen (PSA) is a key biomarker in prostate cancer management.
- Elevated PSA after radical prostatectomy can indicate residual disease or benign prostatic tissue.
- Distinguishing the source of PSA is crucial for patient treatment strategies.
Purpose of the Study:
- To investigate the likelihood of benign prostatic tissue being the source of measurable PSA post-radical prostatectomy.
- To evaluate PSA levels in a cohort of patients with extremely low-risk prostate cancer.
Main Methods:
- A cohort of 1308 men undergoing radical prostatectomy was analyzed.
- 331 patients with extremely low-risk disease (preoperative PSA <10 ng/mL, low Gleason score, etc.) were selected.
- Measurable PSA was defined as 0.05-0.14 ng/mL on two occasions 6 months apart; biochemical recurrence was >0.15 ng/mL.
Main Results:
- In patients with extremely low-risk disease, 0.6% developed measurable PSA and 0.3% had biochemical recurrence.
- Follow-up ranged from 3 months to 6 years (mean 36.2 months).
- The single case of biochemical recurrence responded to salvage radiotherapy, suggesting a malignant origin.
Conclusions:
- Measurable PSA or biochemical recurrence is exceptionally rare in extremely low-risk prostate cancer patients post-prostatectomy.
- Retained benign prostatic elements are unlikely to be the source of elevated PSA in this select group.
- These findings support the interpretation of post-operative PSA elevations as indicative of residual malignancy.
