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Use of [18F]FET PET-MRI to Improve Detection of Pituitary Adenomas in Cushing's Disease (FIND)

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University Hospital Basel

Status

Invitation-only

Conditions

Cushing Disease

Treatments

Diagnostic Test: [18F]FET PET-MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT07108244
FIND study

Details and patient eligibility

About

In ACTH-dependent hypercortisolism it is important to distinguish between Cushing's disease (CD), with ACTH production by a pituitary neuroendocrine tumour (PitNET) and Cushing's syndrome (CS), with ectopic ACTH production. Bilateral inferior petrosal sinus sampling (IPSS) is the gold standard for this distinction, with a diagnostic accuracy of 98%. However, IPSS is an invasive procedure and an indi-rect diagnostic method, rarely providing reliable data on the exact location of the PitNET. This has a major impact on the therapeutic approach, short and long-term remission rates, and other outcomes. Hybrid Positron-emission tomography-Magnetic Resonance Imaging (PET-MRI) using O-(2-[18F]-fluo-roethyl)-L-tyrosine ([18F]FET) is promising in this respect. Recent data published by our research group demonstrate a a sensitivity of 100% a high accuracy in in the precise localization of ACTH-secreting PitNETs. We hypothesize that [18F]FET PET-MRI could become the new non-invasive diagnostic stand-ard, but data regarding a direct comparison between the diagnostic impact of [18F]FET PET-MRI versus IPSS in the differentiation between CD and ectopic CS are lacking. In addition, there are currently no other reliable biomarkers to distinguish the two disorders. The investigators hypothesize that the ACTH-dependent biomarker copeptin could be a valuable addition in this regard. The aim of this prospective diagnostic study is to compare the diagnostic accuracy of [18F]FET-PET-MRI and IPSS in differentiating CD from ectopic CS in patients with ACTH-dependent hypercortisolism.

Enrollment

43 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18 years
  • Biochemically confirmed ACTH-dependent hypercortisolism, defined as:
  • Non-suppressed ACTH levels plus minimal 2 of the following:
  • Overnight 1mg dexamethasone suppression test > 50 nmol/L
  • Elevated late night salivary cortisol (min. 2/3 measurements)
  • Elevated 24-hours urinary free cortisol (min. 2 measurements)
  • Pituitary microadenoma (< 10mm) OR negative / inconclusive findings on standard MRI of the pituitary sella-region.
  • Indication for further evaluation with IPSS

Exclusion criteria

  • Non-ACTH dependent hypercortisolism
  • Pituitary macroadenoma (≥ 10mm)
  • Suspicion of Pseudo-Cushing's disease (e.g. due to alcohol use disorder, PCO's, obesity, de-pression) according to standard work up / guidelines
  • use of glucocorticosteroids
  • Impaired renal function, defined as eGFR (MDRD) <30ml/min/1,73 m2. An exception can be made in consultation with the treating physician.
  • Impaired Liver function
  • Pregnancy/breastfeeding. For the latter, temporary discontinuation may be considered.
  • Known allergic reaction to therapeutic radiopharmaceuticals.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

43 participants in 1 patient group

[18F]FET-PET-MRI vs IPSS for diagnosing CD vs ectopic CS in ACTH-dependent cases
Other group
Description:
Participants will undergo both \[18F\]FET-PET-MRI and inferior petrosal sinus sampling (IPSS) to evaluate their diagnostic performance in differentiating Cushing's disease from ectopic ACTH secretion. Results of both procedures will be made available to the treating medical team and participants as they become available.
Treatment:
Diagnostic Test: [18F]FET PET-MRI

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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