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Study identifier: NCT07463625 Synced from ClinicalTrials.gov · July 28, 2026
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Evaluation of Positron Emission Tomography (PET) With [18F]FET for the Detection of ACTH-Secreting Corticotroph Pituitary Neuroendocrine Tumors.

Condition: Cushing Disease · ACTH-producing Pituitary Tumour  ·  Sponsor: Hospices Civils de Lyon

PhaseN/A
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Cushing's disease results from adrenocorticotropic hormone (ACTH) secretion by corticotroph pituitary neuroendocrine tumors (PitNETs). Magnetic resonance imaging (MRI) is the reference modality for etiological diagnosis but may to visualize small corticotroph microadenomas in up to 30% of the cases, and false positives may occur. The study hypothesis is that positron emission tomography (PET) using \[18F\]fluoroethyl-L-tyrosine (\[18F\]FET) improves localization of ACTH-secreting corticotroph microadenomas compared with MRI and could inform surgical planning and reduce reliance on invasive inferior petrosal sinus sampling. This observational cohort (retrospective and prospective data) will assess the diagnostic performance of \[18F\]FET PET for tumor localization using postoperative histopathology as the gold standard. Secondary aims include: 1. assessing cases in which PET modifies localization relative to MRI and is correct by gold standard; 2. inter-reader agreement between two nuclear medicine physicians; 3. correlations between PET signal and biochemical markers of hypercortisolism 4. uni- and multivariable analyses of clinical and imaging parameters influencing PET results; 5. association between PET findings and subsequent biological remission.

This description comes directly from the study's public registry record.

Talk to the study team

Anthime FLAUS, MD  ·  +33 4 72 35 69 99  ·  anthime.flaus@chu-lyon.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Hôpital Louis Pradel - Service de Médecine NucléaireBron, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07463625