ENTRAP: Exendin PET/CT for Imaging of Paragangliomas

Sponsor
Radboud University Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT05418907
Collaborator
(none)
10
1
13
0.8

Study Details

Study Description

Brief Summary

Functional imaging of paragangliomas (PGLs) is not unequivocal. Existing functional imaging modalities show good but variable results in PGLs, warranting the search for additional molecular imaging targets. Investigators aim to evaluate the glucagon-like peptide 1 receptor (GLP-1R) as a novel target for molecular imaging of PGLs. For this purpose investigators will use the tracer 68Ga-NODAGA-exendin 4 for positron emission tomography/computed tomography (PET/CT) imaging.

Condition or Disease Intervention/Treatment Phase
  • Radiation: 68Ga-NODAGA-exendin-4 PET/CT

Detailed Description

Rationale:

Functional imaging of paragangliomas (PGLs) is not unequivocal. Existing functional imaging modalities show good but variable results in PGLs, warranting the search for additional molecular imaging targets. Investigators aim to evaluate the glucagon-like peptide 1 receptor (GLP-1R) as a novel target for molecular imaging of PGLs. For this purpose investigators will use the tracer 68Ga-NODAGA-exendin 4 for positron emission tomography/computed tomography (PET/CT) imaging.

Objective:

The primary objective is to examine the feasibility of 68Ga-exendin-4 PET/CT for localization and functional characterization of PGLs.

Study design:

In this prospective pilot imaging study 68Ga-exendin-4 PET/CT will be performed in 10 patients with confirmed PGL who have undergone CT, somatostatin receptor (SSTR) PET/CT and 18F-FDG PET/CT (as standard diagnostic procedures) and are scheduled for surgery. 100 ± 10 MBq 68Ga-NODAGA-exendin-4 will be administered to 10 patients in total. In the first 5 patients PET/CT imaging will be performed 1, 2 and 4 hours after injection to determine the optimal imaging timepoint for the remainder of the patients, which will be applied in the remaining patients.

The images will be reconstructed and evaluated by a nuclear medicine physician who is blinded to the results of the CT, SSTR PET/CT and 18F-FDG PET/CT to assess tumor detection. Additionally, quantitative analysis of 68Ga-exendin-4, SSTR PET and 18F-FDG PET/CT images will be performed. After the patients have undergone surgery, immunohistochemical analysis of surgical specimens will be performed to assess GLP-1R expression, which will be compared with in vivo tracer uptake.

Study Design

Study Type:
Observational
Anticipated Enrollment :
10 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Exendin PET/CT for Paragangliomas
Actual Study Start Date :
Jun 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Jul 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Patients with confirmed paraganglioma

10 patients with confirmed PGL who have undergone CT, somatostatin receptor (SSTR) PET/CT and 18F-FDG PET/CT (as standard diagnostic procedures) and are scheduled for surgery.

Radiation: 68Ga-NODAGA-exendin-4 PET/CT
PET/CT imaging 1 hour after injection of 100 MB 68Ga-NODAGA-exendin-4

Outcome Measures

Primary Outcome Measures

  1. detection rate of PGL's using 68Ga-exendin-4 PET/CT [1 year]

    Detection based on visual inspection of PET/CT images

Secondary Outcome Measures

  1. optimal timepoint for imaging PGLs using 68Ga-exendin-4 PET/CT [After inclusion of the first 5 patients (up to 6 months)]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Proven sympathetic PGL with a single tumor detected using standard diagnostic imaging

  • No evidence of metastatic disease

  • CT, SSTR PET/CT and 18F-FDG PET/CT performed (golden standard diagnostic imaging)

  • Scheduled for surgery

  • Able to sign informed consent

Exclusion Criteria:
  • Breast feeding

  • Pregnancy or the wish to become pregnant within 1 month

  • Calculated creatinine clearance below 40ml/min

  • Evidence of other malignancy than PGL in conventional imaging (suspicious liver, bone and lung lesions)

  • Age < 18 years

  • Not able to sign informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Radboud University Medical Center Nijmegen Netherlands 6500 HB

Sponsors and Collaborators

  • Radboud University Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Radboud University Medical Center
ClinicalTrials.gov Identifier:
NCT05418907
Other Study ID Numbers:
  • 2021-000194-93
First Posted:
Jun 14, 2022
Last Update Posted:
Jun 14, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 14, 2022