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A New Technique for Treating Low-risk Prostate Cancer—Super Active Surveillance
Published on: November 7, 2025
Primary cryoablation nadir prostate specific antigen and biochemical failure
David A Levy1, Louis L Pisters, J Stephen Jones
1Department of Regional Urology, Glickman Urological and Kidney Institute, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA. Levyd3@ccf.org
The Journal of Urology
|July 21, 2009
Summary
Nadir prostate specific antigen levels after cryoablation predict long-term outcomes for prostate cancer patients. A PSA level of 0.6 ng/ml or higher indicates a higher risk of biochemical failure, necessitating close monitoring.
Area of Science:
- Oncology
- Urology
Background:
- Prostate cancer is a significant health concern, with cryoablation emerging as a treatment option.
- Assessing treatment efficacy is crucial for patient management and long-term outcomes.
Purpose of the Study:
- To correlate nadir prostate specific antigen (PSA) levels post-cryoablation with long-term biochemical disease-free survival.
- To evaluate the prognostic value of PSA in risk-stratified prostate cancer patients treated with cryoablation.
Main Methods:
- Analysis of data from 2,427 patients in the Cryo On-Line Data Registry.
- Biochemical disease-free survival was assessed using PSA levels up to 60 months post-cryoablation, based on nadir + 2 criteria.
- Patients were stratified into low, intermediate, and high-risk groups.
Main Results:
- For nadir PSA < 0.1 ng/ml, 60-month survival rates ranged from 71% (high-risk) to 91.8% (low-risk).
- For nadir PSA 0.1-0.5 ng/ml, 60-month survival rates ranged from 51% (high-risk) to 86% (low-risk).
- PSA levels of 0.6 ng/ml or greater were associated with a 29.5% biochemical failure rate at 24 months, irrespective of risk group.
Conclusions:
- Nadir PSA after prostate cryoablation serves as a prognostic indicator for biochemical disease-free survival.
- A nadir PSA of 0.6 ng/ml or higher warrants close follow-up due to a significant biochemical failure rate.
- Nadir PSA alone is insufficient to define disease-free survival without correlation to disease-specific or metastasis-free survival.

