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Int. braz. j. urol ; 45(4): 724-731, July-Aug. 2019. tab, graf
Article in English | LILACS | ID: biblio-1019880

ABSTRACT

ABSTRACT Objectives To evaluate the diagnostic performance and interobserver agreement of PI-RADS v2. Materials and Methods In this Institutional Review Board approved single-center retrospective study, 98 patients with clinically suspected PCa who underwent 3-T multiparametric MRI followed by MRI/TRUS fusion-guided prostate biopsy were included from June 2013 to February 2015. Two radiologists (R1 and R2) with 8 and 1 years of experience in abdominal radiology reviewed the MRI scans and assigned PI-RADS v2 scores in all prostate zones. PI-RADS v2 were compared to MRI/TRUS fusion-guided biopsy results, which were classified as negative, PCa, and significant PCa (sPCa). Results Sensitivity, specificity, NPV, PPV and accuracy for PCa was 85.7% (same for all metrics) for R1 and 81.6%, 79.6%, 81.2%, 80.0% and 80.6% for R2. For detecting sPCa, the corresponding values were 95.3%, 85.4%, 95.9%, 83.7% and 89.8% for R1 and 93.0%, 81.8%, 93.7%, 86.7% and 86.7% for R2. There was substantial interobserver agreement in assigning PI-RADS v2 score as negative (1, 2, 3) or positive (4, 5) (Kappa=0.78). On multivariate analysis, PI-RADS v2 (p <0.001) was the only independent predictor of sPCa compared with age, abnormal DRE, prostate volume, PSA and PSA density. Conclusions Our study population demonstrated that PI-RADS v2 had high diagnostic accuracy, substantial interobserver agreement, and it was the only independent predictor of sPCa.


Subject(s)
Humans , Male , Aged , Prostatic Neoplasms/diagnostic imaging , Magnetic Resonance Imaging/methods , Prostatic Neoplasms/pathology , Reference Values , Brazil , Logistic Models , Observer Variation , Reproducibility of Results , Retrospective Studies , Risk Factors , Sensitivity and Specificity , Prostate-Specific Antigen/blood , Statistics, Nonparametric , Risk Assessment , Neoplasm Grading , Image-Guided Biopsy/methods , Middle Aged
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