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dc.contributor.authorSilins, Ien_US
dc.contributor.authorSundin, Aen_US
dc.contributor.authorLubberink, Men_US
dc.contributor.authorO'Sullivan, Len_US
dc.contributor.authorGurnell, Men_US
dc.contributor.authorAigbirhio, Fen_US
dc.contributor.authorBrown, Men_US
dc.contributor.authorWall, Aen_US
dc.contributor.authorÅkerström, Ten_US
dc.contributor.authorRoslin, Sen_US
dc.contributor.authorHellman, Pen_US
dc.contributor.authorAntoni, Gen_US
dc.date.accessioned2023-10-17T10:28:28Z
dc.date.available2022-08-23en_US
dc.date.issued2023-01en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/91345
dc.description.abstractPURPOSE: [11C]Metomidate positron emission tomography (PET) is currently used for staging of adrenocortical carcinoma and for lateralization in primary aldosteronism (PA). Due to the short half-life of carbon-11 and a high non-specific liver uptake of [11C]metomidate there is a need for improved adrenal imaging methods. In a previous pre-clinical study para-chloro-2-[18F]fluoroethyletomidate has been proven to be a specific adrenal tracer. The objective is to perform a first evaluation of para-chloro-2-[18F]fluoroethyletomidate positron emission computed tomography ([18F]CETO-PET/CT) in patients with adrenal tumours and healthy volunteers. METHODS: Fifteen patients underwent [18F]CETO-PET/CT. Five healthy volunteers were recruited for test-retest analysis and three out of the five underwent additional [15O]water PET/CT to measure adrenal blood flow. Arterial blood sampling and tracer metabolite analysis was performed. The kinetics of [18F]CETO were assessed and simplified quantitative methods were validated by comparison to outcome measures of tracer kinetic analysis. RESULTS: Uptake of [18F]CETO was low in the liver and high in adrenals. Initial metabolization was rapid, followed by a plateau. The kinetics of [18F]CETO in healthy adrenals and all adrenal pathologies, except for adrenocortical carcinoma, were best described by an irreversible single-tissue compartment model. Standardized uptake values (SUV) correlated well with the uptake rate constant K1. Both K1 and SUV were highly correlated to adrenal blood flow in healthy controls. Repeatability coefficients of K1, SUV65-70, and SUV120 were 25, 22, and 17%. CONCLUSIONS: High adrenal uptake combined with a low unspecific liver uptake suggests that 18F]CETO is a suitable tracer for adrenal imaging. Adrenal SUV, based on a whole-body scan at 1 h p.i., correlated well with the net uptake rate Ki. TRIAL REGISTRATION: ClinicalTrials.gov , NCT05361083 Retrospectively registered 29 April 2022. at,  https://clinicaltrials.gov/ct2/show/NCT05361083.en_US
dc.format.extent398 - 409en_US
dc.languageengen_US
dc.relation.ispartofEur J Nucl Med Mol Imagingen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectAdrenal traceren_US
dc.subjectPositron emission tomographyen_US
dc.subject[18F]CETOen_US
dc.subjectHumansen_US
dc.subjectPositron Emission Tomography Computed Tomographyen_US
dc.subjectAdrenocortical Carcinomaen_US
dc.subjectKineticsen_US
dc.subjectPositron-Emission Tomographyen_US
dc.subjectAdrenal Cortex Neoplasmsen_US
dc.titleFirst-in-human evaluation of [18F]CETO: a novel tracer for adrenocortical tumours.en_US
dc.typeArticle
dc.identifier.doi10.1007/s00259-022-05957-9en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36074157en_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume50en_US
dcterms.dateAccepted2022-08-23en_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States