AI Article Synopsis

  • * The study analyzed data from 366 men, finding that lower-grade and less aggressive PI resulted in a significantly higher detection rate of csPCa compared to higher-grade and more aggressive PI, with false positive rates also varying accordingly.
  • * The authors conclude that bioptic PI is a significant factor impacting the false positive rates of mp-MRI, suggesting that clinicians need to be cautious about the influence of PI when interpreting MRI results for prostate cancer detection.

Article Abstract

Introduction: The aim of this article was to determine the impact of bioptic prostatic inflammation (PI) on the false positive rate of multiparametric magnetic resonance imaging (mp-MRI) in detecting clinically significant prostate ancer (csPCa).

Material And Methods: Our prostate biopsy database was queried to identify patients who underwent mp-MRI before PB at our institution. A dedicated uropathologist prospectively assessed bioptic PI using the Irani scores. We evaluated the association between mp-MRI findings, bioptic Gleason grade (GG) and aggressiveness of PI, and PCa detection.

Results: In total, 366 men were included. In patients with Prostate Imaging Reporting and Data System (PIRADS) 4-5 lesions, the csPCa (GG ≥2) rate was significantly higher in those with low-grade than in those with high-grade PI (36% vs 29.7%; p = 0.002), and in those with low-aggressive than in those with high-aggressive PI (37.7% vs 30.1%; p = 0.0003). The false positive rates of PIRADS 4-5 lesions for any PCa were 34.2% and 57.8% for low- and high-grade PI, respectively (p = 0.002); similarly, they were 29.5% and 59.4% for mildly and highly-aggressive PI (p = 0.0003). Potential study limitations include its retrospective analysis and single-center study and lack of assessment of the type of PI.

Conclusions: Bioptic PI directly correlates with false positive rates of mp-MRI in detecting csPCa. Clinicians should be aware that PI remains the most common pitfall of mp-MRI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552932PMC
http://dx.doi.org/10.5173/ceju.2021.3.074.R1DOI Listing

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