Abstract

IntroductionMultiple scoring systems have been proposed for prostate MRI reporting. We sought to review the clinical impact of the new Prostate Imaging Reporting and Data System v2 (PI-RADS) and compare those results to our proposed Simplified Qualitative System (SQS) score with respect to detection of prostate cancers and clinically significant prostate cancers.MethodsAll patients who underwent multiparametric prostate MRI (mpMRI) had their images interpreted using PI-RADS v1 and SQS score. PI-RADS v2 was calculated from prospectively collected data points. Patients with positive mpMRIs were then referred by their urologists for enrollment in an IRB-approved prospective phase III trial of mpMRI-Ultrasound (MR/TRUS) fusion biopsy of suspicious lesions. Standard 12-core biopsy was performed at the same setting. Clinical data were collected prospectively.Results1060 patients were imaged using mpMRI at our institution during the study period. 341 participants were then referred to the trial. 312 participants underwent MR/TRUS fusion biopsy of 452 lesions and were included in the analysis. 202 participants had biopsy-proven cancer (64.7%) and 206 (45.6%) lesions were positive for cancer. Distribution of cancer detected at each score produced a Gaussian distribution for SQS while PI-RADS demonstrates a negatively skewed curve with 82.1% of cases being scored as a 4 or 5. Patient-level data demonstrated AUC of 0.702 (95% CI 0.65 to 0.73) for PI-RADS and 0.762 (95% CI 0.72 to 0.81) for SQS (p< 0.0001) with respect to the detection of prostate cancer. The analysis for clinically significant prostate cancer at a per lesion level resulted in an AUC of 0.725 (95% CI 0.69 to 0.76) and 0.829 (95% CI 0.79 to 0.87) for the PI-RADS and SQS score, respectively (p< 0.0001).ConclusionsmpMRI is a useful tool in the workup of patients at risk for prostate cancer, and serves as a platform to guide further evaluation with MR/TRUS fusion biopsy. SQS score provided a more normal distribution of scores and yielded a higher AUC than PI-RADS v2. However until our findings are validated, we recommend reporting of detailed sequence-specific findings. This will allow for prospectively collected data to be utilized in determining the impact of ongoing changes to these scoring systems as our understanding of mpMRI interpretation evolves.

Highlights

  • Multiple scoring systems have been proposed for prostate MRI reporting

  • Until our findings are validated, we recommend reporting of detailed sequence-specific findings. This will allow for prospectively collected data to be utilized in determining the impact of ongoing changes to these scoring systems as our understanding of Multiparametric MRI (mpMRI) interpretation evolves

  • Multiparametric MRI provides high quality imaging of the prostate that results in improved cancer detection with a positive predictive value of 93% [1] and negative predictive value of 95% [2]. mpMRI has been shown to improve risk stratification, enhance patient counseling regarding treatment options, and assist with selection of ideal candidates for active surveillance and other therapies [3,4,5,6]

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Summary

Introduction

Multiple scoring systems have been proposed for prostate MRI reporting. We sought to review the clinical impact of the new Prostate Imaging Reporting and Data System v2 (PIRADS) and compare those results to our proposed Simplified Qualitative System (SQS) score with respect to detection of prostate cancers and clinically significant prostate cancers.Accepted: November 3, 2015Published: November 25, 2015. Multiparametric MRI (mpMRI) provides high quality imaging of the prostate that results in improved cancer detection with a positive predictive value of 93% [1] and negative predictive value of 95% [2]. ACR PI-RADS v2 sought to establish technical parameters for prostate MRI; standardize terminology of reports; facilitate the use of MRI for targeted biopsy; aid in risk stratification; and enhance communication, quality assurance, and research[7, 8]. Overall ACR PI-RADS v2 assessment ( referred to as “PI-RADS”) uses a 5-point scale based on the likelihood that a combination of MRI findings on DWI, T2W, and DCE correlates with the presence of a clinically significant cancer at a particular location in the prostate gland (Figs 1 and 2)

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