Cargando…

FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA)

Disclosure: E. Goodchild: None. R. Senanayake: None. X. Wu: None. W. Bashari: None. J. Salsbury: None. G. Argentesi: None. S.M. O'Toole: None. J. McFarlane: None. K. Laycock: None. D. Gillett: None. I. Boros: None. A. Sahdev: None. N. Bird: None. S. Hader: None. V. Warnes: None. K. Cruickshank:...

Descripción completa

Detalles Bibliográficos
Autores principales: Goodchild, Emily, Senanayake, Russell, Wu, Xilin, Bashari, Waiel, Salsbury, Jackie, Argentesi, Giulia, Matthew O'Toole, Samuel, McFarlane, James, Laycock, Kate, Gillett, Daniel, Boros, Istvan, Sahdev, Anju, Bird, Nicholas, Hader, Stephan, Warnes, Victoria, Cruickshank, Kennedy, Aigbirhio, Franklin, Cheow, Heok, Drake, William, Gurnell, Mark, Jonathan Brown, Morris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554891/
http://dx.doi.org/10.1210/jendso/bvad114.668
_version_ 1785116522973233152
author Goodchild, Emily
Senanayake, Russell
Wu, Xilin
Bashari, Waiel
Salsbury, Jackie
Argentesi, Giulia
Matthew O'Toole, Samuel
McFarlane, James
Laycock, Kate
Gillett, Daniel
Boros, Istvan
Sahdev, Anju
Bird, Nicholas
Hader, Stephan
Warnes, Victoria
Cruickshank, Kennedy
Aigbirhio, Franklin
Cheow, Heok
Drake, William
Gurnell, Mark
Jonathan Brown, Morris
author_facet Goodchild, Emily
Senanayake, Russell
Wu, Xilin
Bashari, Waiel
Salsbury, Jackie
Argentesi, Giulia
Matthew O'Toole, Samuel
McFarlane, James
Laycock, Kate
Gillett, Daniel
Boros, Istvan
Sahdev, Anju
Bird, Nicholas
Hader, Stephan
Warnes, Victoria
Cruickshank, Kennedy
Aigbirhio, Franklin
Cheow, Heok
Drake, William
Gurnell, Mark
Jonathan Brown, Morris
author_sort Goodchild, Emily
collection PubMed
description Disclosure: E. Goodchild: None. R. Senanayake: None. X. Wu: None. W. Bashari: None. J. Salsbury: None. G. Argentesi: None. S.M. O'Toole: None. J. McFarlane: None. K. Laycock: None. D. Gillett: None. I. Boros: None. A. Sahdev: None. N. Bird: None. S. Hader: None. V. Warnes: None. K. Cruickshank: None. F. Aigbirhio: None. H. Cheow: None. W. Drake: None. M. Gurnell: None. M.J. Brown: None. Introduction: Our MATCH study demonstrated 11-C ligand MTO was non-inferior to adrenal vein sampling in predicting adrenalectomy outcomes in patients with PA.(1) The 20-minute half-life of 11-C imposes major logistic constraints. We investigated an 18-F ligand, CETO; its 2 hour half-life permits use in anywhere with fluorodeoxyglucose (FDG)-positron emission tomography (PET) scan facilities. Objective: To determine whether molecular adrenal imaging, using CETO, is as accurate as MTO in predicting which patients with PA will achieve biochemical and/or clinical remission after unilateral adrenalectomy. Methods: This was an extension to the MATCH study (clinical trial number NCT02945904). All patients had an AVS and MTO scanning,(1) and in 31 patients, a second (CETO) scan was performed and interpreted in ignorance of the AVS results. Results: The probability of unilateral APA was in agreement in 27/31 patients (Kappa= 0.76). The number of APAs detected by CETO (18 on the left side, 19 on the right) was similar to MTO (21 left, 19 right) (Wilcoxon P=0.424 and P=0.773). The mean tumour maximum standardised uptake value (SUVmax), by time of flight (TOF), did not differ between CETO (21.9 on the left side, 22.6 on the right) and MTO (22.8 on the left, 24.1 on the right) (Wilcoxon P=0.142). The probability of an adenoma identified by CETO or MTO was very similar: CETO, low 48.4%, medium 22.6%, high 29.0% on the left; low 48.4%, medium 12.9%, high 38.7% on the right; MTO, low 38.7%, medium 19.4% and high 41.9% on left; low 48.4%, medium 16.1%, high 35.5% on the right (Kappa 0.765 for the left and 0.833 for the right). Analysis of scans by SharpIR gave similar probabilities as thee TOF analyses. There was less liver uptake measured by CETO than MTO, (CETO mean 3.7, MTO mean 14.5, Wilcoxon P<0.001). Conclusions: There is no significant difference in the primary outcome of CETO and MTO scans in the investigation of PA. CETO has the potential to be a more favourable ligand, for clinical use, due to its longer half-life, and consequent potential for greater geographical distribution. (18)-F CETO PET-CT imaging has the potential to increase lateralisation rates in PA. References: 1)11C-metomidate PET CT versus Adrenal Vein Sampling for diagnosing surgically curable primary aldosteronism. Nature Medicine https://www.nature.com/articles/s41591-022-02114-5. In press. Presentation: Friday, June 16, 2023
format Online
Article
Text
id pubmed-10554891
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-105548912023-10-06 FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA) Goodchild, Emily Senanayake, Russell Wu, Xilin Bashari, Waiel Salsbury, Jackie Argentesi, Giulia Matthew O'Toole, Samuel McFarlane, James Laycock, Kate Gillett, Daniel Boros, Istvan Sahdev, Anju Bird, Nicholas Hader, Stephan Warnes, Victoria Cruickshank, Kennedy Aigbirhio, Franklin Cheow, Heok Drake, William Gurnell, Mark Jonathan Brown, Morris J Endocr Soc Cardiovascular Endocrinology Disclosure: E. Goodchild: None. R. Senanayake: None. X. Wu: None. W. Bashari: None. J. Salsbury: None. G. Argentesi: None. S.M. O'Toole: None. J. McFarlane: None. K. Laycock: None. D. Gillett: None. I. Boros: None. A. Sahdev: None. N. Bird: None. S. Hader: None. V. Warnes: None. K. Cruickshank: None. F. Aigbirhio: None. H. Cheow: None. W. Drake: None. M. Gurnell: None. M.J. Brown: None. Introduction: Our MATCH study demonstrated 11-C ligand MTO was non-inferior to adrenal vein sampling in predicting adrenalectomy outcomes in patients with PA.(1) The 20-minute half-life of 11-C imposes major logistic constraints. We investigated an 18-F ligand, CETO; its 2 hour half-life permits use in anywhere with fluorodeoxyglucose (FDG)-positron emission tomography (PET) scan facilities. Objective: To determine whether molecular adrenal imaging, using CETO, is as accurate as MTO in predicting which patients with PA will achieve biochemical and/or clinical remission after unilateral adrenalectomy. Methods: This was an extension to the MATCH study (clinical trial number NCT02945904). All patients had an AVS and MTO scanning,(1) and in 31 patients, a second (CETO) scan was performed and interpreted in ignorance of the AVS results. Results: The probability of unilateral APA was in agreement in 27/31 patients (Kappa= 0.76). The number of APAs detected by CETO (18 on the left side, 19 on the right) was similar to MTO (21 left, 19 right) (Wilcoxon P=0.424 and P=0.773). The mean tumour maximum standardised uptake value (SUVmax), by time of flight (TOF), did not differ between CETO (21.9 on the left side, 22.6 on the right) and MTO (22.8 on the left, 24.1 on the right) (Wilcoxon P=0.142). The probability of an adenoma identified by CETO or MTO was very similar: CETO, low 48.4%, medium 22.6%, high 29.0% on the left; low 48.4%, medium 12.9%, high 38.7% on the right; MTO, low 38.7%, medium 19.4% and high 41.9% on left; low 48.4%, medium 16.1%, high 35.5% on the right (Kappa 0.765 for the left and 0.833 for the right). Analysis of scans by SharpIR gave similar probabilities as thee TOF analyses. There was less liver uptake measured by CETO than MTO, (CETO mean 3.7, MTO mean 14.5, Wilcoxon P<0.001). Conclusions: There is no significant difference in the primary outcome of CETO and MTO scans in the investigation of PA. CETO has the potential to be a more favourable ligand, for clinical use, due to its longer half-life, and consequent potential for greater geographical distribution. (18)-F CETO PET-CT imaging has the potential to increase lateralisation rates in PA. References: 1)11C-metomidate PET CT versus Adrenal Vein Sampling for diagnosing surgically curable primary aldosteronism. Nature Medicine https://www.nature.com/articles/s41591-022-02114-5. In press. Presentation: Friday, June 16, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10554891/ http://dx.doi.org/10.1210/jendso/bvad114.668 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Cardiovascular Endocrinology
Goodchild, Emily
Senanayake, Russell
Wu, Xilin
Bashari, Waiel
Salsbury, Jackie
Argentesi, Giulia
Matthew O'Toole, Samuel
McFarlane, James
Laycock, Kate
Gillett, Daniel
Boros, Istvan
Sahdev, Anju
Bird, Nicholas
Hader, Stephan
Warnes, Victoria
Cruickshank, Kennedy
Aigbirhio, Franklin
Cheow, Heok
Drake, William
Gurnell, Mark
Jonathan Brown, Morris
FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA)
title FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA)
title_full FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA)
title_fullStr FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA)
title_full_unstemmed FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA)
title_short FRI156 Novel Radiolabeled Ligand, Para-chloro-2-[(18)F]fluoroethyletomidate (CETO) Is Equivalent To [11C]metomidate-PET (MTO) For The Lateralisation Of Primary Aldosteronism (PA)
title_sort fri156 novel radiolabeled ligand, para-chloro-2-[(18)f]fluoroethyletomidate (ceto) is equivalent to [11c]metomidate-pet (mto) for the lateralisation of primary aldosteronism (pa)
topic Cardiovascular Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554891/
http://dx.doi.org/10.1210/jendso/bvad114.668
work_keys_str_mv AT goodchildemily fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT senanayakerussell fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT wuxilin fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT bashariwaiel fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT salsburyjackie fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT argentesigiulia fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT matthewotoolesamuel fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT mcfarlanejames fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT laycockkate fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT gillettdaniel fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT borosistvan fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT sahdevanju fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT birdnicholas fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT haderstephan fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT warnesvictoria fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT cruickshankkennedy fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT aigbirhiofranklin fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT cheowheok fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT drakewilliam fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT gurnellmark fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa
AT jonathanbrownmorris fri156novelradiolabeledligandparachloro218ffluoroethyletomidatecetoisequivalentto11cmetomidatepetmtoforthelateralisationofprimaryaldosteronismpa