Abstract

Simple SummaryFor the transfer of suspicious lesions in magnetic resonance imaging (MRI) to ultrasound in prostate fusion biopsy, biopsy platforms can be distinguished by rigid or elastic image registration. This study evaluates the detection rate of these different platforms for transperineal fusion-guided prostate biopsy to detect clinically significant prostate cancer under consideration of the surgeon’s learning curve. In our cohort, rigid and elastic registration systems showed a similar prostate cancer detection rate in experienced surgeons, whereas novices seem to benefit from rigid fusion. In the total cohort, targeted fusion biopsy with a rigid registration system outperformed elastic registration target biopsy with a superior significant prostate cancer detection rate, each compared to systematic saturation biopsy. Thus, rigid target biopsy aided in reducing targeting errors that result in missing MRI-visualized significant prostate cancer. These results can provide valuable decision support in selecting a biopsy fusion platform to increase the detection rate and risk stratification of prostate cancer, especially at the beginning of the surgeon’s learning curve.Multiparametric magnetic resonance imaging (mpMRI) and MRI/ultrasound fusion-targeted prostate biopsy (FB) have excellent sensitivity in detecting significant prostate cancer (sPC). FB platforms can be distinguished by rigid (RTB) or elastic image registration (ETB). We compared RTB and ETB by analyzing sPC detection rates of both RTB and ETB at different stages of the surgeons’ learning curve. Patients undergoing RTB between 2015–2017 (n = 502) were compared to patients undergoing ETB from 2017–2019 (n = 437). SPC detection rates were compared by Chi-square-test on patient-basis. Combination of transperineal systematic biopsy and each TB served as reference and sub-analyses were performed for different grades of surgeon’s experience. In the RTB subgroup, 233 men (46%) had sPC, compared to 201 (46%) in the ETB subgroup. RTB alone detected 94% of men with sPC and ETB 87% (p = 0.02). However, for at least intermediate-experienced surgeons (>100 FB), no differences occurred between RTB and ETB. In the total cohort, at least intermediate-experienced surgeons detected significantly more sPC (10%, p = 0.008) than novices. Thus, targeted transperineal MRI/TRUS-FB with a RTB registration system showed a similar sPC detection rate to ETB in experienced surgeons but a superior sPC detection rate to ETB in the total cohort. Low-experienced surgeons seem to benefit from RTB.

Highlights

  • Multiparametric magnetic resonance imaging and mpMRI-guided biopsies of the prostate have an important role in prostate cancer (PC) detection as they improve the detection of clinically significant PC while mitigating insignificant PC [1,2,3,4]

  • We identified a group of 502 patients undergoing RTB from January 2015 until February

  • The two groups were similar in the detection rates of significant prostate cancer (sPC), age, and prostate specific antigen (PSA) level

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Summary

Introduction

Multiparametric magnetic resonance imaging (mpMRI) and mpMRI-guided biopsies of the prostate have an important role in prostate cancer (PC) detection as they improve the detection of clinically significant PC (sPC) while mitigating insignificant PC [1,2,3,4]. The risk assessment by MRI prior to biopsy followed by MRI-guided biopsy has been found to be superior to the standard approach using 12-core transrectal ultrasound (TRUS)-guided biopsy [2]. Demonstrating superior detection rates of sPC, mpMRI has been recommended to be used regularly prior to prostate biopsy even in biopsy-naïve patients [1,2,4]. Performing targeted biopsy (TB) under direct MRI guidance is expensive, timeconsuming, and not widely available. TRUS-guided prostate biopsy, despite the lower detection rates, has the advantages of speed, lower costs, and wider availability [7]. Cognitive or software-guided MRI/TRUS fusion biopsy has become the standard diagnostic procedure to perform MRI-guided biopsy [8,9]. Prostate biopsy can lead to complications such as bleeding and urinary retention [11]

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