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A New Technique for Treating Low-risk Prostate Cancer—Super Active Surveillance
Published on: November 7, 2025
254
A modified Delphi study to develop a practical guide for selecting patients with prostate cancer for active
Samuel W D Merriel1, Daniel Moon2,3, Phil Dundee3
1College of Medicine and Health, University of Exeter, 1.18 College House, St Luke's Campus, Heavitree Road, Exeter, EX1 2LU, UK. s.w.d.merriel@exeter.ac.uk.
BMC Urology
|February 5, 2021
Summary
Active surveillance for lower-risk prostate cancer requires standardized diagnostic tests like PSA, MRI, and biopsy for patient selection. Experts reached consensus on key factors, excluding genetic testing, to guide clinical practice and improve patient outcomes.
Area of Science:
- Oncology
- Urology
- Clinical Practice Guidelines
Background:
- Active surveillance (AS) is a management option for low-risk prostate cancer.
- International variation exists in AS protocols, lacking evidence for optimal approaches.
- Guidance for clinicians is needed to standardize AS practices.
Purpose of the Study:
- To establish international expert consensus on patient selection for active surveillance in prostate cancer.
- To provide evidence-based guidance for clinicians managing low-risk prostate cancer.
Main Methods:
- Modified Delphi approach with online questionnaires and a face-to-face workshop.
- International panel of 12 prostate cancer experts.
- 7-point Likert scale for agreement on AS patient selection criteria.
Main Results:
- Consensus reached on minimum diagnostic tests: PSA, PSA density, Multiparametric MRI, and biopsy (systematic and/or targeted).
- Agreement on patient factors and clinical parameters for AS suitability.
- Genetic and genomic testing not recommended for AS clinical decision-making.
Conclusions:
- International AS practice for low-risk prostate cancer shows inconsistency.
- Areas of common practice identified to inform clinical decision-making.
- Consensus provides a foundation for optimizing AS outcomes.

