Abstract

BackgroundThe aim of this study is to investigate whether quantitative DW metrics can provide additive value to the reliable categorization of lesions within existing PI-RADSv2 guidelines. Fifty-eight patients with clinically suspicious prostate cancer who underwent PR examination, PSA serum levels, sextant TRUS-guided biopsies, and bi-parametric MR imaging were included in the study.ResultsSixty-six lesions were detected by histopathological analysis of surgical specimens. The mean ADC values were significantly lower in tumor than non-tumor tissue. The mean ADC value inversely correlated with Gleason score of tumors with a significant p value < 0.001.Conversely, a positive relationship was found between the ADC ratio (ADC of benign prostatic tissue to prostate cancer) and the pathologic Gleason score with a significant elevation of the ADC ratio along with an increase of the pathologic Gleason score (p < 0.001). ROC curves constructed for the tumor ADC and ADC ratio helped to distinguish pathologically aggressive (Gleason score ≥ 7) from non-aggressive (Gleason score ≤ 6) tumors and to correlate it with PIRADSv2 scoring to predict the presence of clinically significant PCA (PIRADSv2 DW ≥ 4). The ability of the tumor ADC and ADC ratio to predict highly aggressive tumors (GS> 7) was high (AUC for ADC and ADC ratio, 0.946 and 0.897; p = 0.014 and 0.039, respectively). The ADC cut-off value for GS ≥ 7 was < 0.7725 and for GS ≤ 6 was > 0.8620 with sensitivity and specificity 97 and 94%. The cutoff ADC ratio for predicting (GS > 7) was 1.42 and for GS ≤ 6 was > 1.320 with sensitivity and specificity 97 and 92%. By applying this ADC ratio cut-off value the sensitivity and specificity of reader 1 for correct categorization of PIRADSv2 DW > 4 increased from 90 and 68% to 95 and 90% and that of reader 2 increased from 94 and 88% to 97 and 92%, respectively.ConclusionEstimation of DW metrics (ADC and ADC ratio between benign prostatic tissue and prostate cancer) allow the non-invasive assessment of biological aggressiveness of prostate cancer and allow reliable application of the PIRADSv2 scoring to determine clinically significant cancer (DW score > 4) which may contribute in planning initial treatment strategies.

Highlights

  • The aim of this study is to investigate whether quantitative DW metrics can provide additive value to the reliable categorization of lesions within existing PI-RADSv2 guidelines

  • The specific aims of Prostate Imaging Reporting and Data System (PIRADS) 2 were to establish guidelines for minimum acceptable technical parameters in multi-parametric prostate Magnetic resonance imaging (MRI), to simplify and standardize the terminology and content of multi-parametric magnetic resonance imaging (mp-MRI) reports, and to develop assessment categories that summarize the levels of suspicion or risk of having significant prostatic cancer [7]

  • Even for the transition zone (TZ), Diffusion weighted imaging (DWI) enables a final determination of clinically significant cancer (CSC) when the findings of T2-weighted imaging (T2WI) are inconclusive [9].The role of dynamic contrast enhancement in routine evaluation of prostate cancer is uncertain

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Summary

Introduction

The aim of this study is to investigate whether quantitative DW metrics can provide additive value to the reliable categorization of lesions within existing PI-RADSv2 guidelines. Today with the use of multi-parametric magnetic resonance imaging (mp-MRI), accurate diagnosis and grading of prostatic cancer has become increasingly popular It includes a combination of T2-weighted, diffusion weighted, and dynamic contrast-enhanced imaging [4, 5]. The specific aims of PIRADS 2 were to establish guidelines for minimum acceptable technical parameters in multi-parametric prostate MRI, to simplify and standardize the terminology and content of mp-MRI reports, and to develop assessment categories that summarize the levels of suspicion or risk of having significant prostatic cancer [7]. Even for the TZ, DWI enables a final determination of clinically significant cancer (CSC) when the findings of T2-weighted imaging (T2WI) are inconclusive (e.g., a score of 3 on T2WI) [9].The role of dynamic contrast enhancement in routine evaluation of prostate cancer is uncertain. In the PIRADS version 2 suspicious enhancements (focal early enhancement) is considered a minor feature in evaluation [10]

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