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Exendin PET/CT for Imaging of Paragangliomas

Exendin PET/CT for Paragangliomas

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05418907
Acronym
ENTRAP
Enrollment
10
Registered
2022-06-14
Start date
2022-06-01
Completion date
2024-12-01
Last updated
2023-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Paraganglioma

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.

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.

Interventions

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

Sponsors

Radboud University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
detection rate of PGL's using 68Ga-exendin-4 PET/CT1 yearDetection based on visual inspection of PET/CT images

Secondary

MeasureTime frame
optimal timepoint for imaging PGLs using 68Ga-exendin-4 PET/CTAfter inclusion of the first 5 patients (up to 6 months)

Countries

Netherlands

Contacts

Primary ContactMarti Boss, PhD
marti.boss@radboudumc.nl+31243613813

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026