Abstract

Objectives:To compare the effect of different PSA density (PSAD) thresholds on the accuracy for clinically significant prostate cancer (csPCa) of the Prostate Imaging Reporting And Data System v.2.1 (PI-RADSv2.1).Methods:We retrospectively included 123 biopsy-naïve men who underwent multiparametric magnetic resonance imaging (mpMRI) and transperineal mpMRI-targeted and systematic prostate biopsy between April 2019 and October 2020. mpMRI, obtained on a 3.0T magnet with a PI-RADSv2.1-compliant protocol, was read by two radiologists (>1500/>500 mpMRI examinations). csPCa was defined as International Society of Urogenital Pathology grading group ≥2. Receiver operating characteristic analysis was used to calculate per-index lesion sensitivity, specificity, and area under the curve (AUC) of PI-RADSv.2.1 categories after adjusting for PSAD ≥0.10,≥0.15, and ≥0.20 ng/mL ml−1. Per-adjusted category cancer detection rate (CDR) was calculated, and decision analysis performed to compare PSAD-adjusted PI-RADSv.2.1 categories as a biopsy trigger.Results:csPCa prevalence was 43.9%. PSAD-adjustment increased the CDR of PI-RADSv2.1 category 4. Sensitivity/specificity/AUC were 92.6%/53.6%/0.82 for unadjusted PI-RADS, and 85.2%/72.4%/0.84, 62.9%/85.5%/0.83, and 92.4%/53.6%/0.82 when adjusting PI-RADS categories for a 0.10, 0.15, and 0.20 ng/ml ml−1 PSAD threshold, respectively. Triggering biopsy for PI-RADS four lesions and PSAD ≥0.10 ng/mL ml−1 was the strategy with greatest net benefit at 30 and 40% risk probability (0.307 and 0.271, respectively).Conclusions:PI-RADSv2.1 category four with PSAD ≥0.10 ng/mL ml−1 was the biopsy-triggering cut-off with the highest net benefit in the range of expected prevalence for csPCa.Advances in knowledge:0.10 ng/mL ml−1 is the PSAD threshold with higher clinical utility in stratifying the risk for prostate cancer of PI-RADSv.2.1 categories.

Highlights

  • Over the last years, prostate magnetic resonance imaging (MRI) has been validated as a tool to minimize the detection of clinically indolent and maximize the detection of clinically significant, prostate cancer compared to conventional transrectal ultrasound-g­ uided systematic biopsy.[1,2,3,4,5] the high sensitivity and low false-n­ egative rate of prostate MRI account for a potential 30% reduction of unnecessary biopsies in men without clinically significant prostate cancer.[6]

  • Of the 123 men, those with category ≥3 index lesions (75.6%) underwent targeted biopsy plus systematic biopsy, while the remaining 30 men with negative multiparametric magnetic resonance imaging (mpMRI) underwent systematic biopsy only. clinically significant prostate cancer (csPCa) was found in 54/123 men (43.9%; 95% confidence intervals (95% CI) 40.5–70.4), with 27/54 International Society of Urological Pathology (ISUP) 2 cancers (50.0%), 17/54 ISUP 3 cancers (31.5%), 6/54 ISUP 4 cancers (11.1%), and 4/54 ISUP 5 cancers (7.4%)

  • PI-R­ ADS 4h category adjusted for PSA density (PSAD) ≥0.10 ng/ml ml−1 was the biopsy trigger with the greatest net benefit for risk probabilities corresponding to the expected prevalence of csPCa in unselected biopsy-n­ aïve patients

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Summary

Introduction

Prostate magnetic resonance imaging (MRI) has been validated as a tool to minimize the detection of clinically indolent and maximize the detection of clinically significant, prostate cancer compared to conventional transrectal ultrasound-g­ uided systematic biopsy.[1,2,3,4,5] the high sensitivity and low false-n­ egative rate of prostate MRI account for a potential 30% reduction of unnecessary biopsies in men without clinically significant prostate cancer (csPCa).[6]. System (PI-R­ ADS) category 3 findings, which harbor csPCa in 25% of cases only.[8] Most successful attempts to stratify csPCa risk inherent to category 3 observations have relied on PSA density (PSAD), which has been advocated as a tool to differentiate between PI-­RADS 3 lesions requiring biopsy (high PSAD, need to avoid false-­negatives) or not (low PSAD, need to avoid false-­positives).[9] Adjusting PI-R­ ADS categories for PSAD showed the potential to increase cancer detection rate (CDR) in PI-­RADS 1–2 categories,[3,10,11] suggesting that PSAD-­based adjustments might be of value in different PI-­RADS categories

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