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Prospective Evaluation of the Prostate Imaging Reporting and Data System Version 2 for Prostate Cancer Detection.
Mertan, Francesca V; Greer, Matthew D; Shih, Joanna H; George, Arvin K; Kongnyuy, Michael; Muthigi, Akhil; Merino, Maria J; Wood, Bradford J; Pinto, Peter A; Choyke, Peter L; Turkbey, Baris.
Affiliation
  • Mertan FV; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Greer MD; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Shih JH; Division of Cancer Treatment and Diagnosis: Biometric Research Program, National Cancer Institute, National Institutes of Health, Rockville, Maryland.
  • George AK; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Kongnyuy M; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Muthigi A; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Merino MJ; Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Wood BJ; Center for Interventional Oncology, National Cancer Institute and Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, Maryland.
  • Pinto PA; Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Choyke PL; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Turkbey B; Molecular Imaging Program, National Cancer Institute, National Institutes of Health, Bethesda, Maryland. Electronic address: turkbeyi@mail.nih.gov.
J Urol ; 196(3): 690-6, 2016 Sep.
Article in En | MEDLINE | ID: mdl-27101772
ABSTRACT

PURPOSE:

Prostate Imaging Reporting and Data System version 2 (PI-RADSv2) was developed to standardize the interpretation and reporting of multiparametric prostate magnetic resonance imaging and provide guidelines for biopsy of multiparametric magnetic resonance imaging findings. We prospectively evaluated the cancer detection rate at each overall PI-RADSv2 score. MATERIALS AND

METHODS:

This prospective study included 62 consecutive patients with 116 lesions who underwent multiparametric prostate magnetic resonance imaging at 3T with PI-RADSv2 evaluation and subsequent targeted magnetic resonance imaging/transrectal ultrasound fusion guided biopsy and concurrent 12-core systematic prostate biopsy between May and September 2015. Median patient age and prostate specific antigen values were 65.5 years (range 50.3 to 76.6) and 7.10 ng/ml (range 0.47 to 863.0), respectively. Mean lesion size was 12.7 mm overall. Lesion based cancer detection rates for all tumors and for Gleason 3+4 or greater tumors at each PI-RADSv2 score were calculated. Univariate analysis was performed to assess differences in the cancer detection rate among PI-RADSv2 scores.

RESULTS:

A total of 116 lesions in 62 patients were evaluated prospectively (0 PI-RADS 1, 18 PI-RADS 2, 19 PI-RADS 3, 47 PI-RADS 4, 32 PI-RADS 5), and the patients underwent magnetic resonance/transrectal ultrasound fusion guided biopsy and systematic biopsy. Histopathology revealed 55 of 116 (47.4%) cancers (17 Gleason 3+3, 16 Gleason 3+4, 6 Gleason 4+3, 12 Gleason 4+4, 3 Gleason 4+5 and 1 Gleason 5+4). Based on targeted biopsy on a per lesion basis, the overall cancer detection rates of PI-RADS 2, 3, 4 and 5 scores for all tumors was 22.2%, 15.8%, 29.8% and 78.1%, respectively. The cancer detection rate of PI-RADS 2, 3, 4 and 5 scores for Gleason 3+4 or greater tumors was 5.6%, 0%, 21.3% and 75%, respectively. Differences in the cancer detection rate between overall PI-RADS 4 and 5 scores were significant (p <0.001 for Gleason greater than 3+3 and Gleason 3+4 or greater cancers).

CONCLUSIONS:

A PI-RADS score of 5 had the highest prospective cancer detection rate (78%). A PI-RADS score of 4 had only a 30% cancer detection rate, which is lower than expected. Surprisingly, no or few significant cancers were detected at a PI-RADS score of 3 (16%). These early prospective data suggest that current criteria result in a high false-positive rate that lowers the cancer detection rate. Therefore, stricter criteria may be needed in the future to decrease false-positives and increase the cancer detection rate for PI-RADS scores of 3, 4 and 5.
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Full text: 1 Database: MEDLINE Main subject: Prostate / Prostatic Neoplasms / Neoplasm Grading Type of study: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: J Urol Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Prostate / Prostatic Neoplasms / Neoplasm Grading Type of study: Diagnostic_studies / Evaluation_studies / Observational_studies / Prognostic_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: J Urol Year: 2016 Type: Article