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Clinicopathologic Characteristics of Patients Undergoing Prostate Core Biopsy with High-Risk (PI-RADS 5) Lesions by Multiparametric Prostate Magnetic Resonance Imaging.

Login to Access Video or Poster Abstract: MP38-18
Sources of Funding: None

Introduction

Multiparametric Prostate Magnetic Resonance Imaging (mpMRI) utilizes a PI-RADS classification system to identify clinically significant (Gleason score (GS) 7 or higher) prostate adenocarcinoma (PCa) with PI-RADS 5 lesions typically corresponding to a high-risk of clinically significant PCa.

Methods

All patients who underwent mpMRI between 1/1/2015 and 6/30/2016 at a large academic institution were identified. Patients with one or more PI-RADS 5 lesions who underwent an ultrasound-MRI fusion PBx were retrospectively reviewed to assess for presence or absence of PCa, location (targeted vs. 12-core/non-targeted cores), GS, and percentage pattern 4 in GS 7 tumors.

Results

138 patients with PI-RADS 5 lesions {1 lesion (107), 2 lesions (27), 3 lesions (4)} were identified, of which 76 (55%) underwent an in-house MRI fusion PBx. In the targeted cores, 7 (9%) patients had no PCa and 69 (91%) patients showed PCa. In 7 patients without PCa (total 12 PI-RADS 5 lesions), the targeted cores showed extensive simple atrophy (2), florid adenosis (1), central zone histology (2), atypical small acinar proliferation (1), focal high-grade prostatic intraepithelial neoplasia (1), granulomatous inflammation (1), carcinoid (1), focal simple atrophy (2) and focal adenosis (1). Clinically significant PCa was noted in 79% (60/76) cases, {GS 3+4 (35), GS 4+3 (16) and GS 8-10 (9)}. In 7 (9%) patients with GS 7 or higher PCa, the highest GS was found in the non-targeted cores. The median % Gleason pattern 4 in GS 7 tumors was 30 (inter-quartile range = 10-60). Of the remaining 62 (45%) patients who did not receive an MRI fusion PBx, 3 had saturation PBx and 27 had a radical prostatectomy (all show GS 7 or higher PCa); 9 received radiation and/or hormone therapy.

Conclusions

The vast majority of patients (79%) with PI-RADS 5 lesions showed GS 7 or higher PCa on targeted cores; however, a small subset (9%) showed no evidence of malignancy. The benign mimickers of PI-RADS 5 lesions include florid adenosis (1), granulomatous inflammation (1), carcinoid (1), central zone acini (2) and simple atrophy (2). PI-RADS 5 lesions can be biopsied for confirmation of clinically significant disease in the vast majority of cases or used to guide the patient's treatment towards more definitive therapies.

Funding

None

Authors
Joel Friedman
Aaron Udager
Nicole Curci
Chandy Ellimoottil
Rohit Mehra
Scott Tomlins
Jeffrey Montgomery
John Wei
Matthew Davenport
Angela Wu
Lakshmi Kunju
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