Investigating the ability of multiparametric MRI to exclude significant prostate cancer prior to transperineal biopsy
We characterized false negative prostate magnetic resonance imaging (MRI) reporting by using histology derived from MRI-transrectal ultrasound (TRUS)-guided transperineal (MTTP) fusion biopsies. In total, 148 consecutive patients were retrospectively reviewed. Men underwent multiparametric MRI (mpMR...
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Veröffentlicht in: | Canadian Urological Association journal 2015-11, Vol.9 (11-12), p.E853-E858 |
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container_title | Canadian Urological Association journal |
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creator | Serrao, Eva M Barrett, Tristan Wadhwa, Karan Parashar, Deepak Frey, Julia Koo, Brendan C Warren, Anne Y Doble, Andrew Kastner, Christof Gallagher, Ferdia A |
description | We characterized false negative prostate magnetic resonance imaging (MRI) reporting by using histology derived from MRI-transrectal ultrasound (TRUS)-guided transperineal (MTTP) fusion biopsies.
In total, 148 consecutive patients were retrospectively reviewed. Men underwent multiparametric MRI (mpMRI), reported by a consultant/attending radiologist in line with European Society of Urogenital Radiology (ESUR) standards. MTTP biopsy of the lesions was performed according to the Ginsburg recommendations. Cases with an MRI-histology mismatch were identified and underwent a second read by an experienced radiologist. A third review was performed with direct histology comparison to determine a true miss from an MRI-occult cancer. Statistical analysis was performed with McNemar's test.
False negative lesions were identified in 29 MRI examinations (19.6%), with a total of 46 lesions. Most false negative lesions (21/46) were located in the anterior sectors of the prostate. The second read led to a significant decrease of false-negative lesions with 7/29 further studies identified as positive on a patient-by-patient basis (24.1% of studies, p = 0.016) and 11/46 lesions (23.9%; p = 0.001). Of these, 30 lesions following the first read and 23 lesions after the second read were considered significant cancer according to the University College London criteria. However, on direct comparison with histology, most lesions were MRI occult.
We demonstrate that MRI can fail to detect clinically relevant lesions. Improved results were achieved with a second read but despite this, a number of lesions remain MRI-occult. Further advances in imaging are required to reduce false negative results. |
doi_str_mv | 10.5489/cuaj.2895 |
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In total, 148 consecutive patients were retrospectively reviewed. Men underwent multiparametric MRI (mpMRI), reported by a consultant/attending radiologist in line with European Society of Urogenital Radiology (ESUR) standards. MTTP biopsy of the lesions was performed according to the Ginsburg recommendations. Cases with an MRI-histology mismatch were identified and underwent a second read by an experienced radiologist. A third review was performed with direct histology comparison to determine a true miss from an MRI-occult cancer. Statistical analysis was performed with McNemar's test.
False negative lesions were identified in 29 MRI examinations (19.6%), with a total of 46 lesions. Most false negative lesions (21/46) were located in the anterior sectors of the prostate. The second read led to a significant decrease of false-negative lesions with 7/29 further studies identified as positive on a patient-by-patient basis (24.1% of studies, p = 0.016) and 11/46 lesions (23.9%; p = 0.001). Of these, 30 lesions following the first read and 23 lesions after the second read were considered significant cancer according to the University College London criteria. However, on direct comparison with histology, most lesions were MRI occult.
We demonstrate that MRI can fail to detect clinically relevant lesions. Improved results were achieved with a second read but despite this, a number of lesions remain MRI-occult. Further advances in imaging are required to reduce false negative results.</description><identifier>ISSN: 1911-6470</identifier><identifier>ISSN: 1920-1214</identifier><identifier>EISSN: 1920-1214</identifier><identifier>DOI: 10.5489/cuaj.2895</identifier><identifier>PMID: 26788234</identifier><language>eng</language><publisher>Canada: Canadian Urological Association</publisher><subject>Care and treatment ; Development and progression ; Magnetic resonance imaging ; Original Research ; Patient outcomes ; Prostate cancer ; Prostate-specific antigen</subject><ispartof>Canadian Urological Association journal, 2015-11, Vol.9 (11-12), p.E853-E858</ispartof><rights>COPYRIGHT 2015 Canadian Urological Association</rights><rights>Copyright: © 2015 Canadian Urological Association or its licensors 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-db0ca7544ca74e790d09b70471f5eb1e904887ee1e47a585ee387f422014c2a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707904/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707904/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26788234$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Serrao, Eva M</creatorcontrib><creatorcontrib>Barrett, Tristan</creatorcontrib><creatorcontrib>Wadhwa, Karan</creatorcontrib><creatorcontrib>Parashar, Deepak</creatorcontrib><creatorcontrib>Frey, Julia</creatorcontrib><creatorcontrib>Koo, Brendan C</creatorcontrib><creatorcontrib>Warren, Anne Y</creatorcontrib><creatorcontrib>Doble, Andrew</creatorcontrib><creatorcontrib>Kastner, Christof</creatorcontrib><creatorcontrib>Gallagher, Ferdia A</creatorcontrib><title>Investigating the ability of multiparametric MRI to exclude significant prostate cancer prior to transperineal biopsy</title><title>Canadian Urological Association journal</title><addtitle>Can Urol Assoc J</addtitle><description>We characterized false negative prostate magnetic resonance imaging (MRI) reporting by using histology derived from MRI-transrectal ultrasound (TRUS)-guided transperineal (MTTP) fusion biopsies.
In total, 148 consecutive patients were retrospectively reviewed. Men underwent multiparametric MRI (mpMRI), reported by a consultant/attending radiologist in line with European Society of Urogenital Radiology (ESUR) standards. MTTP biopsy of the lesions was performed according to the Ginsburg recommendations. Cases with an MRI-histology mismatch were identified and underwent a second read by an experienced radiologist. A third review was performed with direct histology comparison to determine a true miss from an MRI-occult cancer. Statistical analysis was performed with McNemar's test.
False negative lesions were identified in 29 MRI examinations (19.6%), with a total of 46 lesions. Most false negative lesions (21/46) were located in the anterior sectors of the prostate. The second read led to a significant decrease of false-negative lesions with 7/29 further studies identified as positive on a patient-by-patient basis (24.1% of studies, p = 0.016) and 11/46 lesions (23.9%; p = 0.001). Of these, 30 lesions following the first read and 23 lesions after the second read were considered significant cancer according to the University College London criteria. However, on direct comparison with histology, most lesions were MRI occult.
We demonstrate that MRI can fail to detect clinically relevant lesions. Improved results were achieved with a second read but despite this, a number of lesions remain MRI-occult. Further advances in imaging are required to reduce false negative results.</description><subject>Care and treatment</subject><subject>Development and progression</subject><subject>Magnetic resonance imaging</subject><subject>Original Research</subject><subject>Patient outcomes</subject><subject>Prostate cancer</subject><subject>Prostate-specific antigen</subject><issn>1911-6470</issn><issn>1920-1214</issn><issn>1920-1214</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNptkl9rFDEUxQdRbK0--AUkKIg-TE2ydyYzL0Ip_lmoCtr3kMnemU3JJNMkU7rf3gxdyy74kuQmP869nJyieM3oeQVN-0nP6uacN231pDhlLacl4wyeLmfGyhoEPSlexHhDaZ1vxPPihNeiafgKTot57e4wJjOoZNxA0haJ6ow1aUd8T8bZJjOpoEZMwWjy4_eaJE_wXtt5gySawZneaOUSmYKPSSUkudIYcm18WOAUlIsTBuNQWdIZP8Xdy-JZr2zEV_v9rLj--uX68nt59evb-vLiqtRQ01RuOqqVqADyCihauqFtJygI1lfYMWwpNI1AZAhCVU2FuGpED5xTBpqr1Vnx-UF2mrsRNxpdHsbKPNqowk56ZeTxizNbOfg7mS3L3SALfNgLBH87Z5_kaKJGa5VDP0fJRE1bVjPeZvTdAzooi9K43mdFveDyAgAo1ByqTL39D6UncysPoY9HkPYu4X0a1ByjXP_5eSz4_oDdZovTNno7J-NdPAb3ojp_VAzYP9rAqFxSJJcUySVFmX1z6Nsj-S82q78D8sKg</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Serrao, Eva M</creator><creator>Barrett, Tristan</creator><creator>Wadhwa, Karan</creator><creator>Parashar, Deepak</creator><creator>Frey, Julia</creator><creator>Koo, Brendan C</creator><creator>Warren, Anne Y</creator><creator>Doble, Andrew</creator><creator>Kastner, Christof</creator><creator>Gallagher, Ferdia A</creator><general>Canadian Urological Association</general><general>Canadian Medical Association</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151101</creationdate><title>Investigating the ability of multiparametric MRI to exclude significant prostate cancer prior to transperineal biopsy</title><author>Serrao, Eva M ; Barrett, Tristan ; Wadhwa, Karan ; Parashar, Deepak ; Frey, Julia ; Koo, Brendan C ; Warren, Anne Y ; Doble, Andrew ; Kastner, Christof ; Gallagher, Ferdia A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-db0ca7544ca74e790d09b70471f5eb1e904887ee1e47a585ee387f422014c2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Care and treatment</topic><topic>Development and progression</topic><topic>Magnetic resonance imaging</topic><topic>Original Research</topic><topic>Patient outcomes</topic><topic>Prostate cancer</topic><topic>Prostate-specific antigen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Serrao, Eva M</creatorcontrib><creatorcontrib>Barrett, Tristan</creatorcontrib><creatorcontrib>Wadhwa, Karan</creatorcontrib><creatorcontrib>Parashar, Deepak</creatorcontrib><creatorcontrib>Frey, Julia</creatorcontrib><creatorcontrib>Koo, Brendan C</creatorcontrib><creatorcontrib>Warren, Anne Y</creatorcontrib><creatorcontrib>Doble, Andrew</creatorcontrib><creatorcontrib>Kastner, Christof</creatorcontrib><creatorcontrib>Gallagher, Ferdia A</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Canadian Urological Association journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Serrao, Eva M</au><au>Barrett, Tristan</au><au>Wadhwa, Karan</au><au>Parashar, Deepak</au><au>Frey, Julia</au><au>Koo, Brendan C</au><au>Warren, Anne Y</au><au>Doble, Andrew</au><au>Kastner, Christof</au><au>Gallagher, Ferdia A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigating the ability of multiparametric MRI to exclude significant prostate cancer prior to transperineal biopsy</atitle><jtitle>Canadian Urological Association journal</jtitle><addtitle>Can Urol Assoc J</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>9</volume><issue>11-12</issue><spage>E853</spage><epage>E858</epage><pages>E853-E858</pages><issn>1911-6470</issn><issn>1920-1214</issn><eissn>1920-1214</eissn><abstract>We characterized false negative prostate magnetic resonance imaging (MRI) reporting by using histology derived from MRI-transrectal ultrasound (TRUS)-guided transperineal (MTTP) fusion biopsies.
In total, 148 consecutive patients were retrospectively reviewed. Men underwent multiparametric MRI (mpMRI), reported by a consultant/attending radiologist in line with European Society of Urogenital Radiology (ESUR) standards. MTTP biopsy of the lesions was performed according to the Ginsburg recommendations. Cases with an MRI-histology mismatch were identified and underwent a second read by an experienced radiologist. A third review was performed with direct histology comparison to determine a true miss from an MRI-occult cancer. Statistical analysis was performed with McNemar's test.
False negative lesions were identified in 29 MRI examinations (19.6%), with a total of 46 lesions. Most false negative lesions (21/46) were located in the anterior sectors of the prostate. The second read led to a significant decrease of false-negative lesions with 7/29 further studies identified as positive on a patient-by-patient basis (24.1% of studies, p = 0.016) and 11/46 lesions (23.9%; p = 0.001). Of these, 30 lesions following the first read and 23 lesions after the second read were considered significant cancer according to the University College London criteria. However, on direct comparison with histology, most lesions were MRI occult.
We demonstrate that MRI can fail to detect clinically relevant lesions. Improved results were achieved with a second read but despite this, a number of lesions remain MRI-occult. Further advances in imaging are required to reduce false negative results.</abstract><cop>Canada</cop><pub>Canadian Urological Association</pub><pmid>26788234</pmid><doi>10.5489/cuaj.2895</doi><tpages>E853</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Care and treatment Development and progression Magnetic resonance imaging Original Research Patient outcomes Prostate cancer Prostate-specific antigen |
title | Investigating the ability of multiparametric MRI to exclude significant prostate cancer prior to transperineal biopsy |
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