Gleason Score within Prostate Abnormal Areas Defined by Multiparametric Magnetic Resonance Imaging Did Not Vary

Hakim Slaoui1, Yann Neuzillet, Tarek Ghoneim

  • 1Department of Urology, Hospital Foch, Suresnes, France.

Abstract

Insights

Prostate Imaging Reporting and Data System (PI-RADS) scores do not significantly correlate with Gleason scores from radical prostatectomy specimens or MRI-targeted biopsies. The concordance between biopsy methods and surgical specimens was found to be weak.

Area of Science:

  • Urology
  • Radiology
  • Pathology

Background:

  • Multiparametric magnetic resonance imaging (mpMRI) is increasingly used for prostate cancer detection.
  • The Prostate Imaging Reporting and Data System (PI-RADS) version 2 provides a standardized method for reporting mpMRI findings.
  • Accurate Gleason scoring is crucial for prostate cancer management and treatment decisions.

Purpose of the Study:

  • To correlate PI-RADS version 2 scores with Gleason scores from both radical prostatectomy (RP) specimens and MRI fusion-targeted biopsies (FTB).
  • To evaluate the concordance of Gleason scores between FTB and RP specimens.
  • To compare the concordance of MRI-targeted biopsies with classical biopsies against RP specimens.

Main Methods:

  • Retrospective review of mpMRI from 74 patients who underwent RP after FTB.
  • Comparison of Gleason score distribution based on PI-RADS scores using the Kruskal-Wallis test.
  • Assessment of concordance using Cohen's kappa test for both MRI-targeted and classical biopsies against RP specimens, with a comparison to 903 additional RP specimens and biopsies.

Main Results:

  • An exact match in Gleason grade between RP specimens and FTB was observed in 62% of cases.
  • No significant difference in Gleason score distribution (≤7 vs. ≥7) was found according to PI-RADS scores (p=0.096).
  • Kappa coefficients indicated weak concordance for both MRI-targeted (κ=0.378) and classical biopsies (κ=0.316) compared to RP specimens.

Conclusions:

  • PI-RADS scores did not demonstrate a significant association with Gleason score distribution within the targeted areas.
  • The concordance of Gleason scores between both MRI-targeted biopsies and classical biopsies with radical prostatectomy specimens was weak.
  • These findings suggest limitations in the current ability of PI-RADS to precisely predict Gleason scores and guide biopsy targeting accuracy.