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dc.contributor.authorKarlberg, Anna Maria
dc.contributor.authorBerntsen, Erik Magnus
dc.contributor.authorJohansen, Håkon
dc.contributor.authorSkjulsvik, Anne Jarstein
dc.contributor.authorReinertsen, Ingerid
dc.contributor.authorHong, Yan Dai
dc.contributor.authorXiao, Yiming
dc.contributor.authorRivaz, Hassan
dc.contributor.authorBorghammer, Per
dc.contributor.authorSolheim, Ole
dc.contributor.authorEikenes, Live
dc.date.accessioned2020-03-13T11:53:26Z
dc.date.available2020-03-13T11:53:26Z
dc.date.created2019-07-09T08:35:25Z
dc.date.issued2019
dc.identifier.citationClinical Nuclear Medicine. 2019, 44 (7), 550-559.nb_NO
dc.identifier.issn0363-9762
dc.identifier.urihttp://hdl.handle.net/11250/2646728
dc.description.abstractPurpose This pilot study aimed to evaluate the amino acid tracer 18F-FACBC with simultaneous PET/MRI in diagnostic assessment and neurosurgery of gliomas. Materials and Methods Eleven patients with suspected primary or recurrent low- or high-grade glioma received an 18F-FACBC PET/MRI examination before surgery. PET and MRI were used for diagnostic assessment, and for guiding tumor resection and histopathological tissue sampling. PET uptake, tumor-to-background ratios (TBRs), time-activity curves, as well as PET and MRI tumor volumes were evaluated. The sensitivities of lesion detection and to detect glioma tissue were calculated for PET, MRI, and combined PET/MRI with histopathology (biopsies for final diagnosis and additional image-localized biopsies) as reference. Results Overall sensitivity for lesion detection was 54.5% (95% confidence interval [CI], 23.4–83.3) for PET, 45.5% (95% CI, 16.7–76.6) for contrast-enhanced MRI (MRICE), and 100% (95% CI, 71.5–100.0) for combined PET/MRI, with a significant difference between MRICE and combined PET/MRI (P = 0.031). TBRs increased with tumor grade (P = 0.004) and were stable from 10 minutes post injection. PET tumor volumes enclosed most of the MRICE volumes (>98%) and were generally larger (1.5–2.8 times) than the MRICE volumes. Based on image-localized biopsies, combined PET/MRI demonstrated higher concurrence with malignant findings at histopathology (89.5%) than MRICE (26.3%). Conclusions Low- versus high-grade glioma differentiation may be possible with 18F-FACBC using TBR. 18F-FACBC PET/MRI outperformed MRICE in lesion detection and in detection of glioma tissue. More research is required to evaluate 18F-FACBC properties, especially in grade II and III tumors, and for different subtypes of gliomas.nb_NO
dc.language.isoengnb_NO
dc.publisherLippincott, Williams & Wilkinsnb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.title18F-FACBC PET/MRI in diagnostic assessment and neurosurgery of gliomasnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber550-559nb_NO
dc.source.volume44nb_NO
dc.source.journalClinical Nuclear Medicinenb_NO
dc.source.issue7nb_NO
dc.identifier.doi10.1097/RLU.0000000000002610
dc.identifier.cristin1710731
dc.description.localcode© 2019 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journalnb_NO
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cristin.unitcode194,65,30,0
cristin.unitnameInstitutt for sirkulasjon og bildediagnostikk
cristin.unitnameKlinikk for bildediagnostikk
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameLaboratoriemedisinsk klinikk
cristin.unitnameNasjonal kompetansetjeneste for ultralyd- og bildeveiledet behandling
cristin.unitnameNevroklinikken
cristin.unitnameInstitutt for nevromedisin og bevegelsesvitenskap
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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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