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Updated: Jun 6, 2025

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A Cognitive Fusion-guided Prostate Biopsy Using Multiparametric Magnetic Resonance Imaging and Transrectal Ultrasound
Published on: March 21, 2025
137
Long-Term Risk of Clinically Significant Prostate Cancer in Biopsy-Negative Patients With Baseline Biparametric
Laura Parhiala1,2,3, Juha Knaapila4, Ivan Jambor5,6,7
1Department of Urology, University of Turku, Turku, Finland.
Journal of Magnetic Resonance Imaging : JMRI
|November 27, 2024
Summary
Men with initial negative prostate biopsy and low PI-RADS scores on MRI have a low risk of clinically significant prostate cancer (csPCa). This suggests conservative follow-up may be appropriate for these patients.
Area of Science:
- Radiology
- Oncology
- Urology
Background:
- The long-term prevalence of clinically significant prostate cancer (csPCa) after an initial negative prostate biopsy remains unclear.
- Accurate risk stratification is crucial for managing patients with suspected prostate cancer.
Purpose of the Study:
- To determine the incidence of csPCa in men with initially negative prostate biopsies.
- To evaluate the role of baseline biparametric MRI (bpMRI) and Prostate Imaging Reporting Data System (PI-RADS) scores in predicting csPCa development.
Main Methods:
- Retrospective analysis of prospectively collected data from 197 men with negative initial biopsies and baseline bpMRI.
- BpMRI interpretation using PI-RADS v2.1; biopsy results served as the reference standard.
- Statistical analysis included Kruskal-Wallis, Fisher's exact, Pearson's chi-square tests, and regression analysis; Kaplan-Meier method for time to diagnosis.
Main Results:
- Of 197 men, 38% had PI-RADS 1-2, 29% had PI-RADS 3, and 34% had PI-RADS 4-5.
- During a median follow-up of 52 months, csPCa developed in 8.1% (PI-RADS 1-2), 5.3% (PI-RADS 3), and 18.2% (PI-RADS 4-5) of men.
- Baseline PI-RADS score was the only significant predictor of csPCa diagnosis during follow-up.
Conclusions:
- Men with negative initial biopsies and low baseline bpMRI PI-RADS scores (1-3) exhibit a low rate of csPCa development.
- These findings support a more conservative follow-up strategy for select patient groups.
- Further research with extended follow-up is recommended to validate these observations.

