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Endocrine Abstracts (2024) 99 RC3.2 | DOI: 10.1530/endoabs.99.RC3.2

1University Hospital Würzburg, Division of Endocrinology and Diabetology, Würzburg; 2University Hospital Würzburg, Department of Nuclear Medicine, Würzburg; 3Klinik für Endokrinologie, Diabetologie und Klinische Ernährung, UniversitätsSpital Zürich (USZ) und Universität Zürich (UZH), Switzerland, Switzerland; 4Department of Nuclear Medicine, University Medical Center of the Johannes Gutenberg University Mainz, Germany, Germany; 5University Hospital Leipzig, Medizinische Klinik und Poliklinik III – Endokrinologie, Nephrologie, Rheumatologie, Leipzig, Germany; 6Klinikum der Universität München, Department of Nuclear Medicine, Munich, Germany; 7Department of Endocrinology and Metabolism, I Medical Clinic, University Medical Center of the Johannes Gutenberg University Mainz; 8Department of Nuclear Medicine, West German Cancer Center (WTZ), University Hospital Essen, University of Duisburg-Essen; German Cancer Consortium (DKTK), Partner Site University Hospital Essen; 9Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Nuclear Medicine, 10Klinik und Poliklinik für Nuklearmedizin, Universitätsklinikum Leipzig, 11Institute of Pathology, University of Würzburg, 12Medical Research Council Laboratory of Medical Sciences, London, UK, 13Institute of Medical Bioinformatics and Biostatistics, Philipps University of Marburg


Adrenal tumours are frequently detected by conventional cross-sectional imaging, which, however, has limited specificity in identifying the most prevalent tumour type, benign, non-functional adrenocortical adenomas (ACA) not requiring surgery. We assessed the diagnostic accuracy of adrenal molecular imaging with [18F]Fluorodeoxyglucose-positron emission tomography (FDG-PET) and [123I]Iodometomidate-single photon emission tomography (IMTO-SPECT). We performed a prospective, multicentre study in adult patients (≥30 years) with indeterminate adrenal masses (diameter >3 cm and unenhanced computed tomography [CT] tumour attenuation ≥10 Hounsfield units [HU]). We assessed the diagnostic performance of combined FDG/IMTO imaging in detecting ACA, using a reference standard of histopathology. Low FDG uptake (=FDG-negative) with high IMTO uptake (=IMTO-positive) was considered indicative of ACA. We also assessed the utility of FDG and unenhanced CT tumour attenuation in detecting malignancy. Between July 2015 and December 2020, 85 patients were enrolled and 77 included in the final analysis; 53 harboured benign and 24 malignant adrenal masses. Combined FDG/IMTO-imaging identified ACA with high specificity (95·7% [95%CI 85·2-99·5%]; positive predictive value 87·5% [95%CI 61·7-98·5%]; positive likelihood ratio 11·1 [95%CI 3·2-122·2%]). However, sensitivity was low (48·3% [95%CI 29·4-67·5%]) due to moderate or high FDG uptake in 14 of 30 ACAs. Malignant masses were identified with high sensitivity but low specificity both by unenhanced CT (cut-off HU≥20 sensitivity 100% [95%CI 85·8-100%], specificity 26·4% [95%CI 15·3-40·3%]) and FDG (sensitivity 95·8% [95%CI 78·9-99·9%], specificity 62·3% [95%CI 47·9-75·2%]). Combined FDG/IMTO-imaging identifies ACA with high specificity in this cohort with indeterminate masses. However, the presence of a sub-cohort of FDG-positive ACA decreases sensitivity.

Volume 99

26th European Congress of Endocrinology

Stockholm, Sweden
11 May 2024 - 14 May 2024

European Society of Endocrinology 

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