Abstract
You have accessJournal of UrologyCME1 May 2022MP58-19 COMPARISON OF URONAV TRUS AND COGNITIVE FUSION TP BIOPSY IN DETECTION OF CLINICALLY SIGNIFICANT PROSTATE CANCER Amanda Sherman, Daneil Kuftinec, Lori Lyn Price, Alireza Moinzadeh, and William Faust Amanda ShermanAmanda Sherman More articles by this author , Daneil KuftinecDaneil Kuftinec More articles by this author , Lori Lyn PriceLori Lyn Price More articles by this author , Alireza MoinzadehAlireza Moinzadeh More articles by this author , and William FaustWilliam Faust More articles by this author View All Author Informationhttps://doi.org/10.1097/JU.0000000000002641.19AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract INTRODUCTION AND OBJECTIVE: Transperineal (TP) prostate biopsy is a safe and effective technique to sample the prostate gland with less risk of infection and bleeding. Targeting of abnormal lesions on MRI at time of biopsy can be performed with cognitive fusion or software-based platforms. The success of TP MRI-guided biopsy, particularly cognitive fusion, remains unclear. This study compares cancer detection rates between software-based transrectal US (TRUS)/MRI fusion biopsy and cognitive fusion TP prostate biopsy. METHODS: Biopsies (n=495) taken between 2019 and 2021 were performed using either TRUS with UroNav (TRUSUN) guidance, or via TP approach with cognitive fusion (TPCF) to target MRI lesion. Demographic characteristics, PSA, prostate volume, DRE status, highest PIRADS lesion on MRI and final biopsy pathology were collected. Cancer Detection Rate (CDR), clinically significant Cancer Detection Rate (csCDR), and clinically significant cancer detection rate in target only (csCDRt) were compared by technique type. Statistical analysis was performed using Chi-squared, Fisher's exact, and t-tests as appropriate. RESULTS: A total of 377 TRUSUN and 118 TPCF prostate biopsies were performed. TPCF detected more cancers of any grade (p=0.02), but there was no difference in csCDR or csCDRt. When stratified by lesion, there was no difference in cancer detection except in the PIRADS 5 group, where TPCF outperformed TRUSUN biopsy in detecting clinically significant prostate cancer (p=0.006). Further analysis of the PIRADS 5 group found no difference in baseline characteristics except for age (mean age 72.2y in TP group, 68.7y in TRUS p=0.008). CONCLUSIONS: TPCF prostate biopsy showed similar rates of csCDR and csCDRt as TRUSUN prostate biopsy. When analyzed by PI-RADS score, TPCF was found to have similar or, in the case of PI-RADS 5 lesion, superior csCDRt. Subgroup analysis did not find significant group differences, aside from age, to explain this finding. This data suggests that TPCF is as effective at detecting clinically significant prostate cancer as TRUSUN. Source of Funding: None © 2022 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 207Issue Supplement 5May 2022Page: e999 Advertisement Copyright & Permissions© 2022 by American Urological Association Education and Research, Inc.MetricsAuthor Information Amanda Sherman More articles by this author Daneil Kuftinec More articles by this author Lori Lyn Price More articles by this author Alireza Moinzadeh More articles by this author William Faust More articles by this author Expand All Advertisement PDF DownloadLoading ...
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