Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28584
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dc.contributor.authorBischof, Gérard N-
dc.contributor.authorBartenstein, Peter-
dc.contributor.authorBarthel, Henryk-
dc.contributor.authorvan Berckel, Bart-
dc.contributor.authorDoré, Vincent-
dc.contributor.authorvan Eimeren, Thilo-
dc.contributor.authorFoster, Norman-
dc.contributor.authorHammes, Jochen-
dc.contributor.authorLammertsma, Adriaan A-
dc.contributor.authorMinoshima, Satoshi-
dc.contributor.authorRowe, Chris-
dc.contributor.authorSabri, Osama-
dc.contributor.authorSeibyl, John-
dc.contributor.authorVan Laere, Koen-
dc.contributor.authorVandenberghe, Rik-
dc.contributor.authorVillemagne, Victor L-
dc.contributor.authorYakushev, Igor-
dc.contributor.authorDrzezga, Alexander-
dc.date2021-03-12-
dc.date.accessioned2022-01-10T04:56:29Z-
dc.date.available2022-01-10T04:56:29Z-
dc.date.issued2021-07-01-
dc.identifier.citationJournal of Nuclear Medicine 2021; 62(7): 999-1005en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28584-
dc.description.abstractTo date, 3 18F-labeled PET tracers have been approved for assessing cerebral amyloid plaque pathology in the diagnostic workup of suspected Alzheimer disease (AD). Although scanning protocols are relatively similar across tracers, U.S. Food and Drug Administration- and the European Medicines Agency-approved visual rating protocols differ among the 3 tracers. This proof-of-concept study assessed the comparability of the 3 approved visual rating protocols to classify a scan as amyloid-positive or -negative, when applied by groups of experts and nonexperts to all 3 amyloid tracers. Methods: In an international multicenter approach, both expert (n = 4) and nonexpert raters (n = 3) rated scans acquired with 18F-florbetaben, 18F-florbetapir and 18F-flutemetamol. Scans obtained with each tracer were presented for reading according to all 3 approved visual rating protocols. In a randomized order, every single scan was rated by each reader according to all 3 protocols. Raters were blinded for the amyloid tracer used and asked to rate each scan as positive or negative, giving a confidence judgment after each response. Percentage of visual reader agreement, interrater reliability, and agreement of each visual read with binary quantitative measures (fixed SUV ratio threshold for positive or negative scans) were computed. These metrics were analyzed separately for expert and nonexpert groups. Results: No significant differences in using the different approved visual rating protocols were observed across the different metrics of agreement in the group of experts. Nominal differences suggested that the 18F-florbetaben visual rating protocol achieved the highest interrater reliability and accuracy especially under low confidence conditions. For the group of nonexpert raters, significant differences between the different visual rating protocols were observed with overall moderate-to-fair accuracy and with the highest reliability for the 18F-florbetapir visual rating protocol. Conclusion: We observed high interrater agreement despite applying different visual rating protocols for all 18F-labeled amyloid tracers. This implies that the results of the visual interpretation of amyloid imaging can be well standardized and do not depend on the rating protocol in experts. Consequently, the creation of a universal visual assessment protocol for all amyloid imaging tracers appears feasible, which could benefit especially the less-experienced readers.en
dc.language.isoeng-
dc.subjectamyloid PETen
dc.subjectflorbetabenen
dc.subjectflorbetapiren
dc.subjectflutemetamolen
dc.subjectvisual rating standardizationen
dc.titleToward a Universal Readout for 18F-Labeled Amyloid Tracers: The CAPTAINs Study.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Nuclear Medicine : Official Publication, Society of Nuclear Medicineen
dc.identifier.affiliationMolecular Imaging and Therapyen
dc.identifier.affiliationUniversity Hospital Cologne, Multimodal Neuroimaging Group, Department of Nuclear Medicine, Cologne, Germanyen
dc.identifier.affiliationCSIRO Health and Biosecurity, Parkville 3052, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurology, University Hospital Cologne, Cologne, Germanyen
dc.identifier.affiliationGerman Center of Neurodegenerative Disease (DZNE), Bonn, Germanyen
dc.identifier.affiliationDepartment of Nuclear Medicine, LMU Munich, Munich, Germanyen
dc.identifier.affiliationUniversity Hospital of Leipzig, Department of Nuclear Medicine, Leipzig, Germanyen
dc.identifier.affiliationAmsterdam University Medical Centers, Location VUmc Radiology and Nuclear Medicine, Amsterdam, The Netherlandsen
dc.identifier.affiliationDepartment of Radiology and Imaging Sciences, University of Utah, Salt Lake City, Utahen
dc.identifier.affiliationInstitute for Neurodegenerative Disorders, New Haven, Connecticuten
dc.identifier.affiliationNuclear Medicine and Molecular Imaging, University Hospital Leuven and Department of Imaging and Pathology KU Leuven, Leuven, Belgiumen
dc.identifier.affiliationMemory Clinic, University Hospital Leuven and Department of Neurosciences, KU Leuven, Belgiumen
dc.identifier.affiliationDepartment of Nuclear Medicine, Technical University of Munich, Germanyen
dc.identifier.affiliationInstitute of Neuroscience and Medicine (INM-2), Molecular Organization of the Brain, Forschungszentrum Jülich, Germanyen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/33712532/en
dc.identifier.doi10.2967/jnumed.120.250290en
dc.type.contentTexten
dc.identifier.orcid0000-0002-8051-0558en
dc.identifier.orcid0000-0003-3910-2453en
dc.identifier.orcid0000-0002-5832-9875en
dc.identifier.pubmedid33712532-
local.name.researcherDoré, Vincent
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptMolecular Imaging and Therapy-
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