IMPEC: Impact of [11C]-Methionine PET/MRI in the Detection of Pituitary Adenomas Secreting ACTH and Causing Cushing's Disease

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Completed
CT.gov ID
NCT03346954
Collaborator
(none)
33
1
1
32.7
1

Study Details

Study Description

Brief Summary

Cushing's disease is characterized by the existence of a benign pituitary tumor developed from corticotropic cells responsible for excessive ACTH secretion. This results in hypercorticism causing high morbidity and mortality and severely impairing quality of life. The etiological diagnosis is based on Magnetic Resonance Imaging (MRI). However, pituitary MRI revealed a pituitary tumor in only 60% of patients. The diagnostic procedure is complicated by the existence of extra pituitary tumors responsible for ACTH ectopic secretion. This rare etiology imposes, in the absence of typical pituitary image, the realization of catheterization of the lower petrosal sinuses. Treatment of Cushing's disease is based on transsphenoidal surgical management, even in the absence of a formal MRI image, if pituitary origin is confirmed by the catheterization. Although pituitary surgery without identified target is part of French recommendations, this surgery is associated with a high risk of failure and morbidity. Optimization of the management of patients' with Cushing's disease thus requires the improvement of the diagnostic methods.

Hypothesis of our study is that [11C] MET MRI-PET may be performed as a first-line MRI for suspected Cushing's disease and may limit indications for catheterization of lower petrosal sinuses. Its localizing value should also make it possible to improve the surgical results with a better identification of the adenoma

Condition or Disease Intervention/Treatment Phase
  • Other: [11C]-Methionine PET/MRI
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Impact of [11C]-Methionine PET/MRI in the Detection of Pituitary Adenomas Secreting ACTH and Causing Cushing's Disease
Actual Study Start Date :
Dec 11, 2017
Actual Primary Completion Date :
Jun 11, 2019
Actual Study Completion Date :
Aug 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients with Cushing's disease

Implementation of [11C]-Methionine PET/MRI

Other: [11C]-Methionine PET/MRI
Implementation [11C]-Methionine PET/MRI performed for each patient in one place (department of nuclear medicine of the Hospices Civils de Lyon). The [11C]-Methionine PET/MRI will be performed after a pituitary MRI and before a transsphenoidal surgery.

Outcome Measures

Primary Outcome Measures

  1. Sensitivity of [11C]-Methionine PET/MRI [Within 3 months and 3 weeks after inclusion]

    Sensitivity of [11C]-Methionine PET/MRI to correctly localizes the pituitary corticotropic adenoma in comparison with the sensitivity of the pituitary MRI. The gold standard being the localization defined by anatomopathological analysis on operative resection.

Secondary Outcome Measures

  1. False negatives and false positives description [Within 3 months and 3 weeks after inclusion]

    Description of false negatives and false positives [11C]-Methionine PET/MRI to identify and localize the microadenoma. Characteristics of unidentified adenomas will be described using: volume, localization, type of fixation

  2. Description of identified microadenomas [Within 3 months and 3 weeks months after inclusion]

    Proportion of microadenomas identified by the [11C]-Methionine PET/MRI as a function of the degree of aggressiveness of the adenoma, evaluated by the number of mitoses, the level of expression of Ki67 and p53.

  3. Comparison of [11C]-Methionine PET/MRI and pituitary MRI [Within 3 months and 3 weeks months after inclusion]

    Study of the concordance between the results of [11C]-Methionine PET/MRI and pituitary MRI

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged 18 years old or over

  • Patient with a diagnosed Cushing's disease according to the French "protocole national de diagnostic et de soins (PNDS)"

  • Patient who underwent a MRI pituitary for diagnostic purposes

  • Patient who have undergone catheterization of the lower petrosal sinuses (if MRI does not detect pituitary adenoma) and have a result in favor of a central secretion of ACTH

  • Patient having an indication of surgical excision of the adenoma

  • Patient with a micro-adenoma (less than 1 cm in diameter) if the tumor is visualized on MRI

  • Patient for which informed and written consent to participate has been obtained.

Exclusion Criteria:
    • Patient participating in another study
  • Patient with a pituitary macro-adenoma with visual impairment

  • Patient with ACTH-dependent Cushing's syndrome secondary to ectopic ACTH secretion

  • Patient with recurrence and / or history of pituitary adenoma excision

  • Patient with a contraindication to pituitary surgery or general anesthesia

  • Pregnant woman, breastfeeding or old enough to have children but without effective recognized contraception

  • Contra-indication to the realization of an MRI: permanently fixed metal parts (pacemaker, cerebral clip, cephalic end piercing, cochlear implant, pin or screw for recent bone fracture, dental equipment, metal splinters), claustrophobia

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service de Médecine Nucléaire - Hospices Civils de Lyon Bron France 69677

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

  • Study Director: BOURNAUD Claire, MD, Hospices Civils de Lyon

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT03346954
Other Study ID Numbers:
  • 69HCL17_0167
  • 2017-002721-38
First Posted:
Nov 20, 2017
Last Update Posted:
Dec 1, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hospices Civils de Lyon
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 1, 2020