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dc.contributor.authorEsmaeili, Morteza
dc.contributor.authorTayari, Nassim
dc.contributor.authorScheenen, Tom WJ
dc.contributor.authorElschot, Mattijs
dc.contributor.authorSandsmark, Elise
dc.contributor.authorBertilsson, Helena
dc.contributor.authorHeerschap, Arend
dc.contributor.authorSelnæs, Kirsten Margrete
dc.contributor.authorBathen, Tone Frost
dc.date.accessioned2019-09-18T14:00:15Z
dc.date.available2019-09-18T14:00:15Z
dc.date.created2019-02-27T09:57:35Z
dc.date.issued2018
dc.identifier.citationFrontiers in Oncology. 2018, 8 .nb_NO
dc.identifier.issn2234-943X
dc.identifier.urihttp://hdl.handle.net/11250/2617487
dc.description.abstractPurpose: To investigate the associations of metabolite levels derived from magnetic resonance spectroscopic imaging (MRSI) and 18F-fluciclovine positron emission tomography (PET) with prostate tissue characteristics. Methods: In a cohort of 19 high-risk prostate cancer patients that underwent simultaneous PET/MRI, we evaluated the diagnostic performance of MRSI and PET for discrimination of aggressive cancer lesions from healthy tissue and benign lesions. Data analysis comprised calculations of correlations of mean standardized uptake values (SUVmean), maximum SUV (SUVmax), and the MRSI-derived ratio of (total choline + spermine + creatine) to citrate (CSC/C). Whole-mount histopathology was used as gold standard. Results: The results showed a moderate significant correlation between both SUVmean and SUVmax with CSC/C ratio. Conclusions: We demonstrated that the simultaneous acquisition of 18F-fluciclovine PET and MRSI with an integrated PET/MRI system is feasible and a combination of these imaging modalities has potential to improve the diagnostic sensitivity and specificity of prostate cancer lesions.nb_NO
dc.language.isoengnb_NO
dc.publisherFrontiers Medianb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleSimultaneous 18F-fluciclovine Positron Emission Tomography and Magnetic Resonance Spectroscopic Imaging of Prostate Cancernb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber7nb_NO
dc.source.volume8nb_NO
dc.source.journalFrontiers in Oncologynb_NO
dc.identifier.doi10.3389/fonc.2018.00516
dc.identifier.cristin1680965
dc.description.localcode© 2018 Esmaeili, Tayari, Scheenen, Elschot, Sandsmark, Bertilsson, Heerschap, Selnæs and Bathen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).nb_NO
cristin.unitcode194,65,25,0
cristin.unitcode194,65,15,0
cristin.unitcode1920,2,0,0
cristin.unitcode1920,4,0,0
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameKirurgisk klinikk
cristin.unitnameKlinikk for bildediagnostikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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