Predicitve Value of FDG Uptake in the Remaining Adrenal Gland Following Adrenalectomy for Adrenocortical Cancer.


Journal

Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
ISSN: 1439-4286
Titre abrégé: Horm Metab Res
Pays: Germany
ID NLM: 0177722

Informations de publication

Date de publication:
Jan 2021
Historique:
pubmed: 22 10 2020
medline: 1 10 2021
entrez: 21 10 2020
Statut: ppublish

Résumé

Following initial surgery, patients with adrenocortical carcinoma (ACC) are commonly treated with the adrenolytic substance mitotane in an adjuvant or therapeutic setting. Treatment responses, however, are variable. The objective of the study was to investigate a possible correlation between FDG-PET activity of the remaining adrenal gland and therapeutic response of mitotane treatment. This is a retrospective study enrolling patients from two German centers with operated ACC and minimal information on PET-CT scanning. Eighty-two ACC patients after adrenalectomy were included (66 treated with mitotane and 16 without medical therapy). FDG uptake of the contralateral adrenal gland, liver and mediastinum was analyzed from a total of 291 PET/CT scans (median 4 scans per patient) and correlated with clinical annotations including overall and recurrence free survival. The majority of patients (81%) displayed a temporary increase in adrenal FDG uptake within the first 18 months following surgery, which was not associated with a morphological correlate for potential malignancy. This increase was mainly present in patients treated with mitotane (51/61, 84%) but less frequent in the control group (4/7, 57%). No direct correlation with mitotane plasma levels were evident. Patients following R0 resection with high adrenal uptake showed a tendency towards better clinical outcome without reaching a significance value (HR 1.41; CI 0.42-4.75; p=0.059). FDG update of the contralateral adrenal gland may not be misinterpreted as sign of malignancy but might be rather associated with a trend towards better clinical outcome.

Identifiants

pubmed: 33086388
doi: 10.1055/a-1268-8301
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D
Mitotane 78E4J5IB5J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

24-31

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

The authors declare that they have no conflict of interest.

Auteurs

Ruben Loewe (R)

Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.

Natalie Rogowski-Lehmann (N)

Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.

Thomas Pfluger (T)

Klinik und Poliklink für Nuklearmedizin, Klinikum der Universität München, Munich, Germany.

Martin Reincke (M)

Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.

Stefanie Hahner (S)

Department of Medicine, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.

Christina Bluemel (C)

Department of Nuclear Medicine, University Hospital, University of Würzburg, Würzburg, Germany.

Martin Fassnacht (M)

Department of Medicine, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.
Comprehensive Cancer Center Mainfranken, University of Würzburg, Würzburg, Germany.

Felix Beuschlein (F)

Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Munich, Germany.
Klinik für Endokrinologie, Diabetologie und Klinische Ernährung, Universitätsspital Zürich, Zürich, Switzerland.

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Classifications MeSH