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dc.contributor.authorBarrett, Tristanen
dc.contributor.authorPatterson, Andrewen
dc.contributor.authorKoo, Brendan Cen
dc.contributor.authorWadhwa, Karanen
dc.contributor.authorWarren, Anneen
dc.contributor.authorDoble, Andrewen
dc.contributor.authorGnanapragasam, Vincenten
dc.contributor.authorKastner, Christofen
dc.contributor.authorGallagher, Ferdiaen
dc.date.accessioned2015-07-24T14:06:07Z
dc.date.available2015-07-24T14:06:07Z
dc.date.issued2015en
dc.identifier.citationWorld Journal of Urology 2015. doi: 10.1007/s00345-015-1650-0en
dc.identifier.issn0724-4983
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/249067
dc.description.abstractPurpose To compare histological outcomes in patients undergoing MRI-transrectal ultrasound fusion transperineal (MTTP) prostate biopsy and determine the incremental benefit of targeted cores. Methods 76 consecutive patients with 89 MRI-identified targets underwent MTTP biopsy. Separate targeted biopsies and background cores were obtained according to a standardized protocol. Target biopsies were considered of added diagnostic value if these cores showed a higher Gleason grade than non-targeted cores taken from the same sector (Group 1, n = 41). Conversely, where background cores demonstrated an equal or higher Gleason grade, target cores were considered to be non-beneficial (Group 2, n = 48). Results There was no significant difference in age, PSA, prostate volume, time-to-biopsy, or number of cores obtained between the groups. A greater proportion of target cores were positive for cancer (158/228; 69.3%) compared to background (344/1881; 18.38%). The median target volume was 0.54 cm^3 for Group 1 (range 0.09 - 2.79 cm^3), and 1.65 cm^3 for Group 2 (0.3 - 9.07 cm^3); p <0.001. The targets in Group 1 had statistically lower diameters for short and long axes, even after correction for gland size. The highest area under the receiver operating characteristic curve was demonstrated when a lesion cut-off value of 1.0 cm in short axis was applied, resulting in a sensitivity of 83.3% and specificity of 82.9%. Conclusions When a combined systematic and targeted transperineal prostate biopsy is performed, there is limited benefit in acquiring additional cores from larger volume targets with a short axis diameter greater than 1.0 cm.
dc.description.sponsorshipThe authors acknowledge research support from Cancer Research UK, National Institute of Health Research Cambridge Biomedical Research Centre, Cancer Research UK and the Engineering and Physical Sciences Research Council Imaging Centre in Cambridge and Manchester and the Cambridge Experimental Cancer Medicine Centre.
dc.languageEnglishen
dc.language.isoenen
dc.publisherSpringer
dc.rightsCreative Commons Attribution 4.0
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectImage-Guided Biopsyen
dc.subjectMagnetic Resonance Imagingen
dc.subjectUltrasounden
dc.subjectTransperinealen
dc.subjectProstate Canceren
dc.titleTargeted transperineal biopsy of the prostate has limited additional benefit over background cores for larger MRI-identified tumorsen
dc.typeArticle
dc.description.versionThis is the final version of the article. It first appeared from Springer via http://dx.doi.org/10.1007/s00345-015-1650-0en
prism.publicationDate2015en
prism.publicationNameWorld Journal of Urologyen
dc.rioxxterms.funderCRUK
dc.rioxxterms.funderNIH
dc.rioxxterms.funderEPSRC
dcterms.dateAccepted2015-07-21en
rioxxterms.versionofrecord10.1007/s00345-015-1650-0en
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.licenseref.startdate2015en
dc.contributor.orcidBarrett, Tristan [0000-0002-1180-1474]
dc.contributor.orcidWarren, Anne [0000-0002-1170-7867]
dc.contributor.orcidGnanapragasam, Vincent [0000-0003-4722-4207]
dc.contributor.orcidGallagher, Ferdia [0000-0003-4784-5230]
dc.identifier.eissn1433-8726
rioxxterms.typeJournal Article/Reviewen
pubs.funder-project-idCancer Research UK (16628)
pubs.funder-project-idPROSTATE CANCER UK (PA14-012)


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Creative Commons Attribution 4.0
Except where otherwise noted, this item's licence is described as Creative Commons Attribution 4.0