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Published on: February 19, 2021
Complementing the active surveillance criteria with multiparametric magnetic resonance imaging
Tae Un Kim1, Seung Ryong Baek2, Won Hoon Song2
1Department of Radiology, Pusan National University Yangsan Hospital, Yangsan, Korea.
Multiparametric MRI (mpMRI) helps identify clinically significant prostate cancer (PCa) missed by systematic biopsy. PI-RADS 5 scores indicate unfavorable disease in active surveillance (AS) candidates, suggesting mpMRI improves PCa detection.
Area of Science:
- Urology
- Radiology
- Oncology
Background:
- Active surveillance (AS) is an option for low-risk prostate cancer (PCa).
- Accurate risk stratification is crucial to avoid misclassification.
- Multiparametric magnetic resonance imaging (mpMRI) may improve diagnostic accuracy.
Purpose of the Study:
- To assess the utility of mpMRI in preventing misclassification of patients with clinically significant PCa into AS.
- To determine if mpMRI can identify patients who might benefit from treatment rather than AS.
Main Methods:
- Retrospective analysis of patients with Gleason grade group (GG) 1 PCa undergoing mpMRI before radical prostatectomy (RP).
- Comparison of mpMRI (PI-RADS scores) and pathology results between AS and NOT-AS candidates.
- Definition of unfavorable disease as T3-4 disease or GG upgrade in RP specimens.
Main Results:
- No significant difference in PI-RADS scores between AS and NOT-AS candidates.
- Among AS candidates, 37.5% had GG upgrading and 39.1% had unfavorable disease post-RP.
- Patients with PI-RADS 5 scores had a significantly higher rate of unfavorable disease (83.3%) compared to those with PI-RADS ≤4 (34.5%).
- PI-RADS 5 lesions in AS candidates were often anterior, with 75% showing GG upgrading on targeted biopsy.
Conclusions:
- PI-RADS scores alone did not significantly differentiate AS candidates from those needing treatment.
- mpMRI, particularly PI-RADS 5 lesions, identified a high rate of unfavorable disease in AS candidates.
- Anterior prostate lesions, including in the transitional zone, may be missed by systematic biopsy but detected by mpMRI.
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