Histology core-specific evaluation of the European Society of Urogenital Radiology (ESUR) standardised scoring system of multiparametric magnetic resonance imaging (mpMRI) of the prostate

Objectives To evaluate the Prostate Imaging Reporting and Data System (PIRADS) in multiparametric magnetic resonance imaging (mpMRI) based on single cores and single-core histology. To calculate positive (PPV) and negative predictive values (NPV) of different modalities of mpMRI. Patients and Method...

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Hauptverfasser: Kuru, Timur Hasan (VerfasserIn) , Röthke, Matthias C. (VerfasserIn) , Rieker, Philip (VerfasserIn) , Roth, Wilfried (VerfasserIn) , Fenchel, Michael Christian (VerfasserIn) , Hohenfellner, Markus (VerfasserIn) , Schlemmer, Heinz-Peter (VerfasserIn) , Hadaschik, Boris (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 23 May 2013
In: BJU international
Year: 2013, Jahrgang: 112, Heft: 8, Pages: 1080-1087
ISSN:1464-410X
DOI:10.1111/bju.12259
Online-Zugang:Verlag, Volltext: https://doi.org/10.1111/bju.12259
Verlag, Volltext: https://bjui-journals.onlinelibrary.wiley.com/doi/abs/10.1111/bju.12259
Volltext
Verfasserangaben:Timur H. Kuru, Matthias C. Roethke, Philip Rieker, Wilfried Roth, Michael Fenchel, Markus Hohenfellner, Heinz-Peter Schlemmer and Boris A. Hadaschik

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520 |a Objectives To evaluate the Prostate Imaging Reporting and Data System (PIRADS) in multiparametric magnetic resonance imaging (mpMRI) based on single cores and single-core histology. To calculate positive (PPV) and negative predictive values (NPV) of different modalities of mpMRI. Patients and Methods We performed MRI-targeted transrectal ultrasound-guided perineal prostate biopsies on 50 patients (mean age 66 years, mean PSA level of 9.9 ng/mL) with suspicion of prostate cancer. The biopsy trajectories of every core taken were documented in three dimensions (3D) in a 3D-prostate model. Every core was evaluated separately for prostate cancer and the performed biopsy trajectories were projected on mpMRI images. PIRADS scores of 1177 cores were then assessed by a histology ‘blinded’ uro-radiologist in T2-weighted (T2W), dynamic contrast-enhanced (DCE), diffusion-weighted imaging (DWI) and magnetic resonance spectroscopy (MRS). Results The PIRADS score was significantly higher in cores positive for cancer than in negative cores. There was a significant correlation between the PIRADS score and histopathology for every modality. Receiver operating characteristic (ROC) analysis showed excellent specificity for T2W (90% peripheral zone/97% transition zone) and DWI (98%/97%) images regardless of the prostate region observed. These numbers decreased for DCE (80%/93%) and MRS (76%/83%). All modalities had NPVs of 99%, if a PIRADS score threshold of 2 (for T2W, DCE, and MRS) or 3 (for DWI) was used. However, PPVs were low. Conclusions Our results show that PIRADS scoring is feasible for clinical routine and allows standardised reporting. PIRADS can be used as a decision-support system for targeting of suspicious lesions. mpMRI has a high NPV for prostate cancer and, thus, might be a valuable tool in the initial diagnostic evaluation. 
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