<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Silins I</submitter><funding>Akademiska Sjukhuset</funding><funding>Uppsala University</funding><funding>Medical Research Council</funding><funding>Medical Research Council of the United Kingdom</funding><pagination>398-409</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9816205</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>50(2)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>[&lt;sup>11&lt;/sup>C]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 [&lt;sup>11&lt;/sup>C]metomidate there is a need for improved adrenal imaging methods. In a previous pre-clinical study para-chloro-2-[&lt;sup>18&lt;/sup>F]fluoroethyletomidate has been proven to be a specific adrenal tracer. The objective is to perform a first evaluation of para-chloro-2-[&lt;sup>18&lt;/sup>F]fluoroethyletomidate positron emission computed tomography ([&lt;sup>18&lt;/sup>F]CETO-PET/CT) in patients with adrenal tumours and healthy volunteers.&lt;h4>Methods&lt;/h4>Fifteen patients underwent [&lt;sup>18&lt;/sup>F]CETO-PET/CT. Five healthy volunt</pubmed_abstract><journal>European journal of nuclear medicine and molecular imaging</journal><pubmed_title>First-in-human evaluation of [&amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;F]CETO: a novel tracer for adrenocortical tumours.</pubmed_title><pmcid>PMC9816205</pmcid><funding_grant_id>MR/P01710X/1</funding_grant_id><pubmed_authors>Antoni G</pubmed_authors><pubmed_authors>Brown M</pubmed_authors><pubmed_authors>Wall A</pubmed_authors><pubmed_authors>Aigbirhio F</pubmed_authors><pubmed_authors>Silins I</pubmed_authors><pubmed_authors>Lubberink M</pubmed_authors><pubmed_authors>O'Sullivan L</pubmed_authors><pubmed_authors>Gurnell M</pubmed_authors><pubmed_authors>Roslin S</pubmed_authors><pubmed_authors>Sundin A</pubmed_authors><pubmed_authors>Hellman P</pubmed_authors><pubmed_authors>Akerstrom T</pubmed_authors></additional><is_claimable>false</is_claimable><name>First-in-human evaluation of [&amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;F]CETO: a novel tracer for adrenocortical tumours.</name><description>&lt;h4>Purpose&lt;/h4>[&lt;sup>11&lt;/sup>C]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 [&lt;sup>11&lt;/sup>C]metomidate there is a need for improved adrenal imaging methods. In a previous pre-clinical study para-chloro-2-[&lt;sup>18&lt;/sup>F]fluoroethyletomidate has been proven to be a specific adrenal tracer. The objective is to perform a first evaluation of para-chloro-2-[&lt;sup>18&lt;/sup>F]fluoroethyletomidate positron emission computed tomography ([&lt;sup>18&lt;/sup>F]CETO-PET/CT) in patients with adrenal tumours and healthy volunteers.&lt;h4>Methods&lt;/h4>Fifteen patients underwent [&lt;sup>18&lt;/sup>F]CETO-PET/CT. Five healthy volunt</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-05-27T23:14:52.48Z</modification><creation>2024-12-04T12:40:47.955Z</creation></dates><accession>S-EPMC9816205</accession><cross_references><pubmed>36074157</pubmed><doi>10.1007/s00259-022-05957-9</doi></cross_references></HashMap>