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First-in-human evaluation of [18F]CETO : a novel tracer for adrenocortical tumours

Silins, Isabella, 1983- (author)
Uppsala universitet,Endokrinkirurgi
Sundin, Anders, 1954- (author)
Uppsala universitet,Radiologi
Lubberink, Mark, 1972- (author)
Uppsala universitet,Radiologi
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O'Sullivan, Lleah (author)
Uppsala universitet,Institutionen för kirurgiska vetenskaper
Gurnell, Mark (author)
Institute of Metabolic Science & Department of Medicine, University of Cambridge, Cambridge, UK
Aigbirhio, Franklin (author)
Wolfson Brain Imaging Centre, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK
Brown, Morris (author)
William Harvey Heart Centre, Queen Mary University of London, London, UK
Wall, Anders (author)
Uppsala universitet,Radiologi
Åkerström, Tobias (author)
Uppsala universitet,Endokrinkirurgi
Roslin, Sara (author)
Uppsala universitet,Preparativ läkemedelskemi
Hellman, Per (author)
Uppsala universitet,Endokrinkirurgi
Antoni, Gunnar (author)
Uppsala universitet,Preparativ läkemedelskemi
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 (creator_code:org_t)
2022-09-08
2023
English.
In: European Journal of Nuclear Medicine and Molecular Imaging. - : Springer Nature. - 1619-7070 .- 1619-7089. ; 50:2, s. 398-409
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Purpose[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.MethodsFifteen 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.ResultsUptake 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%.ConclusionsHigh 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 registrationClinicalTrials.gov, NCT05361083 Retrospectively registered 29 April 2022. at, https://clinicaltrials.gov/ct2/show/NCT05361083

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Radiologi och bildbehandling (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Radiology, Nuclear Medicine and Medical Imaging (hsv//eng)

Keyword

[18F]CETO
Adrenal tracer
Positron emission tomography
Surgery
Kirurgi

Publication and Content Type

ref (subject category)
art (subject category)

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