Targeted vs systematic robot‐assisted transperineal magnetic resonance imaging‐transrectal ultrasonography fusion prostate biopsy

Objective To evaluate the performance of transperineal robot‐assisted (RA) targeted (TB) and systematic (SB) prostate biopsy in primary and repeat biopsy settings. Patients and Methods Patients underwent RA biopsy between 2014 and 2016. Before RA‐TB, multiparametric magnetic resonance imaging (mpMRI...

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Veröffentlicht in:BJU international 2018-05, Vol.121 (5), p.791-798
Hauptverfasser: Mischinger, Johannes, Kaufmann, Sascha, Russo, Giorgio I., Harland, Niklas, Rausch, Steffen, Amend, Bastian, Scharpf, Marcus, Loewe, Lorenz, Todenhoefer, Tilman, Notohamiprodjo, Mike, Nikolaou, Konstantin, Stenzl, Arnulf, Bedke, Jens, Kruck, Stephan
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container_end_page 798
container_issue 5
container_start_page 791
container_title BJU international
container_volume 121
creator Mischinger, Johannes
Kaufmann, Sascha
Russo, Giorgio I.
Harland, Niklas
Rausch, Steffen
Amend, Bastian
Scharpf, Marcus
Loewe, Lorenz
Todenhoefer, Tilman
Notohamiprodjo, Mike
Nikolaou, Konstantin
Stenzl, Arnulf
Bedke, Jens
Kruck, Stephan
description Objective To evaluate the performance of transperineal robot‐assisted (RA) targeted (TB) and systematic (SB) prostate biopsy in primary and repeat biopsy settings. Patients and Methods Patients underwent RA biopsy between 2014 and 2016. Before RA‐TB, multiparametric magnetic resonance imaging (mpMRI) was performed. Prostate lesions were scored (Prostate Imaging, Reporting and Data System, version 2) and used for RA‐TB planning. In addition, RA‐SB was performed. Available, whole‐gland pathology was analysed. Results In all, 130 patients were biopsy naive and 72 had had a previous negative transrectal ultrasonography‐guided biopsy. In total, 202 patients had suspicious mpMRI lesions. Clinically significant prostate cancer was found in 85% of all prostate cancer cases (n = 123). Total and clinically significant prostate cancer detection rates for RA‐TB vs RA‐SB were not significantly different at 77% vs 84% and 80% vs 82%, respectively. RA‐TB demonstrated a better sampling performance compared to RA‐SB (26.4% vs 13.9%; P < 0.001). Conclusion Transperineal RA‐TB and ‐SB showed similar clinically significant prostate cancer detection rates in primary and repeat biopsy settings. However, RA‐TB offered a 50% reduction in biopsy cores. Omitting RA‐SB is associated with a significant risk of missing clinically significant prostate cancer.
doi_str_mv 10.1111/bju.14089
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Patients and Methods Patients underwent RA biopsy between 2014 and 2016. Before RA‐TB, multiparametric magnetic resonance imaging (mpMRI) was performed. Prostate lesions were scored (Prostate Imaging, Reporting and Data System, version 2) and used for RA‐TB planning. In addition, RA‐SB was performed. Available, whole‐gland pathology was analysed. Results In all, 130 patients were biopsy naive and 72 had had a previous negative transrectal ultrasonography‐guided biopsy. In total, 202 patients had suspicious mpMRI lesions. Clinically significant prostate cancer was found in 85% of all prostate cancer cases (n = 123). Total and clinically significant prostate cancer detection rates for RA‐TB vs RA‐SB were not significantly different at 77% vs 84% and 80% vs 82%, respectively. RA‐TB demonstrated a better sampling performance compared to RA‐SB (26.4% vs 13.9%; P &lt; 0.001). Conclusion Transperineal RA‐TB and ‐SB showed similar clinically significant prostate cancer detection rates in primary and repeat biopsy settings. However, RA‐TB offered a 50% reduction in biopsy cores. Omitting RA‐SB is associated with a significant risk of missing clinically significant prostate cancer.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/bju.14089</identifier><identifier>PMID: 29211932</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Aged ; Biopsy ; Early Detection of Cancer - instrumentation ; Humans ; Image-Guided Biopsy ; Magnetic resonance imaging ; Magnetic Resonance Imaging, Interventional ; Male ; Middle Aged ; mpMRI‐TRUS fusion ; NMR ; Nuclear magnetic resonance ; PCSM ; Performance evaluation ; Perineum - diagnostic imaging ; Prostate - diagnostic imaging ; Prostate - pathology ; Prostate cancer ; Prostate Imaging Reporting and Data System ; ProstateCancer ; Prostatic Neoplasms - diagnostic imaging ; Prostatic Neoplasms - pathology ; Rectum - diagnostic imaging ; Reproducibility of Results ; Retrospective Studies ; robot‐assisted transperineal prostate biopsy ; Sensitivity and Specificity ; targeted biopsy ; Ultrasonic imaging ; Ultrasonography, Interventional ; Ultrasound</subject><ispartof>BJU international, 2018-05, Vol.121 (5), p.791-798</ispartof><rights>2017 The Authors BJU International © 2017 BJU International Published by John Wiley &amp; Sons Ltd</rights><rights>2017 The Authors BJU International © 2017 BJU International Published by John Wiley &amp; Sons Ltd.</rights><rights>BJUI © 2018 BJU International</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3889-22bab30754fa1aab9486c637a7741d6015433b619c4ae4949aef1ba99e58f1823</citedby><cites>FETCH-LOGICAL-c3889-22bab30754fa1aab9486c637a7741d6015433b619c4ae4949aef1ba99e58f1823</cites><orcidid>0000-0003-4687-7353 ; 0000-0002-8514-3371</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbju.14089$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbju.14089$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29211932$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mischinger, Johannes</creatorcontrib><creatorcontrib>Kaufmann, Sascha</creatorcontrib><creatorcontrib>Russo, Giorgio I.</creatorcontrib><creatorcontrib>Harland, Niklas</creatorcontrib><creatorcontrib>Rausch, Steffen</creatorcontrib><creatorcontrib>Amend, Bastian</creatorcontrib><creatorcontrib>Scharpf, Marcus</creatorcontrib><creatorcontrib>Loewe, Lorenz</creatorcontrib><creatorcontrib>Todenhoefer, Tilman</creatorcontrib><creatorcontrib>Notohamiprodjo, Mike</creatorcontrib><creatorcontrib>Nikolaou, Konstantin</creatorcontrib><creatorcontrib>Stenzl, Arnulf</creatorcontrib><creatorcontrib>Bedke, Jens</creatorcontrib><creatorcontrib>Kruck, Stephan</creatorcontrib><title>Targeted vs systematic robot‐assisted transperineal magnetic resonance imaging‐transrectal ultrasonography fusion prostate biopsy</title><title>BJU international</title><addtitle>BJU Int</addtitle><description>Objective To evaluate the performance of transperineal robot‐assisted (RA) targeted (TB) and systematic (SB) prostate biopsy in primary and repeat biopsy settings. Patients and Methods Patients underwent RA biopsy between 2014 and 2016. Before RA‐TB, multiparametric magnetic resonance imaging (mpMRI) was performed. Prostate lesions were scored (Prostate Imaging, Reporting and Data System, version 2) and used for RA‐TB planning. In addition, RA‐SB was performed. Available, whole‐gland pathology was analysed. Results In all, 130 patients were biopsy naive and 72 had had a previous negative transrectal ultrasonography‐guided biopsy. In total, 202 patients had suspicious mpMRI lesions. Clinically significant prostate cancer was found in 85% of all prostate cancer cases (n = 123). Total and clinically significant prostate cancer detection rates for RA‐TB vs RA‐SB were not significantly different at 77% vs 84% and 80% vs 82%, respectively. RA‐TB demonstrated a better sampling performance compared to RA‐SB (26.4% vs 13.9%; P &lt; 0.001). Conclusion Transperineal RA‐TB and ‐SB showed similar clinically significant prostate cancer detection rates in primary and repeat biopsy settings. However, RA‐TB offered a 50% reduction in biopsy cores. 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Kaufmann, Sascha ; Russo, Giorgio I. ; Harland, Niklas ; Rausch, Steffen ; Amend, Bastian ; Scharpf, Marcus ; Loewe, Lorenz ; Todenhoefer, Tilman ; Notohamiprodjo, Mike ; Nikolaou, Konstantin ; Stenzl, Arnulf ; Bedke, Jens ; Kruck, Stephan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3889-22bab30754fa1aab9486c637a7741d6015433b619c4ae4949aef1ba99e58f1823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aged</topic><topic>Biopsy</topic><topic>Early Detection of Cancer - instrumentation</topic><topic>Humans</topic><topic>Image-Guided Biopsy</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging, Interventional</topic><topic>Male</topic><topic>Middle Aged</topic><topic>mpMRI‐TRUS fusion</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>PCSM</topic><topic>Performance evaluation</topic><topic>Perineum - diagnostic imaging</topic><topic>Prostate - diagnostic imaging</topic><topic>Prostate - pathology</topic><topic>Prostate cancer</topic><topic>Prostate Imaging Reporting and Data System</topic><topic>ProstateCancer</topic><topic>Prostatic Neoplasms - diagnostic imaging</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Rectum - diagnostic imaging</topic><topic>Reproducibility of Results</topic><topic>Retrospective Studies</topic><topic>robot‐assisted transperineal prostate biopsy</topic><topic>Sensitivity and Specificity</topic><topic>targeted biopsy</topic><topic>Ultrasonic imaging</topic><topic>Ultrasonography, Interventional</topic><topic>Ultrasound</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mischinger, Johannes</creatorcontrib><creatorcontrib>Kaufmann, Sascha</creatorcontrib><creatorcontrib>Russo, Giorgio I.</creatorcontrib><creatorcontrib>Harland, Niklas</creatorcontrib><creatorcontrib>Rausch, Steffen</creatorcontrib><creatorcontrib>Amend, Bastian</creatorcontrib><creatorcontrib>Scharpf, Marcus</creatorcontrib><creatorcontrib>Loewe, Lorenz</creatorcontrib><creatorcontrib>Todenhoefer, Tilman</creatorcontrib><creatorcontrib>Notohamiprodjo, Mike</creatorcontrib><creatorcontrib>Nikolaou, Konstantin</creatorcontrib><creatorcontrib>Stenzl, Arnulf</creatorcontrib><creatorcontrib>Bedke, Jens</creatorcontrib><creatorcontrib>Kruck, Stephan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>BJU international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mischinger, Johannes</au><au>Kaufmann, Sascha</au><au>Russo, Giorgio I.</au><au>Harland, Niklas</au><au>Rausch, Steffen</au><au>Amend, Bastian</au><au>Scharpf, Marcus</au><au>Loewe, Lorenz</au><au>Todenhoefer, Tilman</au><au>Notohamiprodjo, Mike</au><au>Nikolaou, Konstantin</au><au>Stenzl, Arnulf</au><au>Bedke, Jens</au><au>Kruck, Stephan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeted vs systematic robot‐assisted transperineal magnetic resonance imaging‐transrectal ultrasonography fusion prostate biopsy</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2018-05</date><risdate>2018</risdate><volume>121</volume><issue>5</issue><spage>791</spage><epage>798</epage><pages>791-798</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>Objective To evaluate the performance of transperineal robot‐assisted (RA) targeted (TB) and systematic (SB) prostate biopsy in primary and repeat biopsy settings. Patients and Methods Patients underwent RA biopsy between 2014 and 2016. Before RA‐TB, multiparametric magnetic resonance imaging (mpMRI) was performed. Prostate lesions were scored (Prostate Imaging, Reporting and Data System, version 2) and used for RA‐TB planning. In addition, RA‐SB was performed. Available, whole‐gland pathology was analysed. Results In all, 130 patients were biopsy naive and 72 had had a previous negative transrectal ultrasonography‐guided biopsy. In total, 202 patients had suspicious mpMRI lesions. Clinically significant prostate cancer was found in 85% of all prostate cancer cases (n = 123). Total and clinically significant prostate cancer detection rates for RA‐TB vs RA‐SB were not significantly different at 77% vs 84% and 80% vs 82%, respectively. RA‐TB demonstrated a better sampling performance compared to RA‐SB (26.4% vs 13.9%; P &lt; 0.001). Conclusion Transperineal RA‐TB and ‐SB showed similar clinically significant prostate cancer detection rates in primary and repeat biopsy settings. However, RA‐TB offered a 50% reduction in biopsy cores. Omitting RA‐SB is associated with a significant risk of missing clinically significant prostate cancer.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29211932</pmid><doi>10.1111/bju.14089</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-4687-7353</orcidid><orcidid>https://orcid.org/0000-0002-8514-3371</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Biopsy
Early Detection of Cancer - instrumentation
Humans
Image-Guided Biopsy
Magnetic resonance imaging
Magnetic Resonance Imaging, Interventional
Male
Middle Aged
mpMRI‐TRUS fusion
NMR
Nuclear magnetic resonance
PCSM
Performance evaluation
Perineum - diagnostic imaging
Prostate - diagnostic imaging
Prostate - pathology
Prostate cancer
Prostate Imaging Reporting and Data System
ProstateCancer
Prostatic Neoplasms - diagnostic imaging
Prostatic Neoplasms - pathology
Rectum - diagnostic imaging
Reproducibility of Results
Retrospective Studies
robot‐assisted transperineal prostate biopsy
Sensitivity and Specificity
targeted biopsy
Ultrasonic imaging
Ultrasonography, Interventional
Ultrasound
title Targeted vs systematic robot‐assisted transperineal magnetic resonance imaging‐transrectal ultrasonography fusion prostate biopsy
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