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Endocrine Abstracts (2019) 65 OP1.3 | DOI: 10.1530/endoabs.65.OP1.3

Adrenal and Cardiovascular

Combining 11C-metomidate PET/CT and 18F-FDG PET/CT – a new approach to phenotyping indeterminate adrenal lesions

Russell Senanayake1,2, Waiel Bashari1,2, Chad Bisambar2, Iosif Mendichovszky2, Heok Cheow2, Vasilis Kosmoliaptsis2, Ruth Casey2 & Mark Gurnell1,2


1University of Cambridge, School of Clinical Medicine, Cambridge, UK; 2Addenbrooke’s Hospital, Cambridge, UK

Background: 11C-Metomidate (MTO)-PET/CT has recently found utility as an alternative to adrenal vein sampling for lateralisation in primary aldosteronism. MTO binds with high affinity to 11b-hydroxylase (CYP11B1) and aldosterone synthase (CYP11B2) and can be considered an adrenocortical-specific tracer. We and others have therefore hypothesised that combining MTO-PET/CT with 18F-FDG(FDG)-PET/CT would permit indeterminate adrenal lesions to be categorised in terms of (i) adrenocortical origin (MTO positive) or not (MTO negative) and (ii) malignant potential (as determined by extent of FDG positivity).

Method: Eight patients (4 male, 4 female) with a new indeterminate adrenal lesion were investigated using MTO-PET/CT and FDG-PET/CT (single centre, 2015–2019). Intensity and distribution of tracer uptake was independently assessed by two radiologists. Histological confirmation of the adrenal lesion was available for six patients.

Results: Benign and malignant lesions of adrenocortical and non-adrenocortical origin were correctly identified using dual PET studies. MTO uptake was only seen in lesions of adrenocortical origin, whereas high level FDG uptake reliably identified malignant lesions (Table 1).

Table 1
Side of lesionLeftLeftRightRightRightLeftRightRight
Metomidate uptakePositiveNegativePositiveNegativeNegativeNegativeNegativeNegative
FDG uptakeLowLowHighHighHighHighHighHigh
CategoryAdC BenignNon-AdC BenignAdC MalignantNon-AdC MalignantNon-AdC MalignantNon-AdC MalignantNon-AdC MalignantNon-AdC Malignant
DiagnosisACA*GNACCAdrenal Met*Phaeo1LymphomaLymphomaLymphoma
Key: ACA, adrenocortical adenoma; ACC, adrenocortical carcinoma; AdC, adrenocortical; FDG, 18F-FDG; GN, ganglioneuroma; Met, metastasis; MTO, 11C-metomidate; Phaeo, phaeochromocytoma; *histological confirmation of diagnosis not available; 1 patient with normal normetanephrine and borderline raised metanephrines levels.

Conclusion: In this proof-of-concept study MTO- and FDG-PET-CT reliably distinguished between benign from malignant, and adrenocortical from non-adrenocortical, lesions. Further studies are required to confirm these findings.

Volume 65

Society for Endocrinology BES 2019

Brighton, United Kingdom
11 Nov 2019 - 13 Nov 2019

Society for Endocrinology 

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