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CXCR4-PET/CT for Diagnosing Giant Cell Arteritis

Not Applicable
Completed
Conditions
Vasculitis
Diagnoses Disease
Interventions
Diagnostic Test: CXCR4-PET
Registration Number
NCT05604482
Lead Sponsor
Matthias Fröhlich
Brief Summary

Giant cell arteritis (GCA) is the most common vasculitis in the elderly. Accurate diagnosis is of utmost importance in order to then initiate the necessary immunosuppressive therapy. For large-vessel GCA (LV-GCA) involving the aorta and its branches, FDG-PET/CT is the standard in imaging for diagnosis and is recommended by the guidelines. However, this only indirectly visualizes inflammation through vessel wall uptake of glucose. A new PET tracer, 68Ga-pentixafor, is used to visualize the chemokine receptor CXCR4. This receptor is expressed by cells of the immune system. In the context of inflammatory processes, upregulation of CXCL12, the ligand of CXCR4, occurs in affected tissues. The chemotactic effect of this ligand leads to the immigration of CXCR4-positive inflammatory cells into the inflamed area, which can be visualized by PET using the CXCR4-specific tracer 68Ga-Pentixafor. The value of CXCR4-PET should therefore be tested in the context of LV-GCA. This study tests the benefit of CXCR4 in therapy-naïve patients with suspected LV-GCA. For this purpose, patients will receive a FDG-PET and a CXCR4-PET for direct comparison. This is an imaging-only study. Therapy will not be affected by the study. The study is single-arm and not blinded.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • New diagnosis of GCA within 5 days of diagnosis or initiation or intensification of therapy.
  • Evidence of inflammatory activity based on clinical parameters, elevated serologic markers of inflammation (CRP > 1.0 mg/dl), or a positive imaging finding on vasculitis MRI, CCDS, or FDG-PET/CT
  • Ability of the patient to provide information
  • Exclusion of contraindications for the performance of a PET/CT examination (see below)
Exclusion Criteria
  • Contraindications for the performance of a PET CT examination
  • Pregnancy
  • Allergies
  • Lack of capacity of the patient to give informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
CXCR4-PET experimental groupCXCR4-PETIn addition to the current standard of imaging in GCA, using FDG-PET/CT, participants receive CXCR4-PET.
Primary Outcome Measures
NameTimeMethod
Maximum measurable tracer activity on 68Ga-Pentixafor PET/CT in the area of blood vessels in active GCA2 years

detection of maximum measurable tracer activity on 68Ga-Pentixafor PET/CT in the area of blood vessels after a maximum of 5 days after diagnosis or when acute inflammatory activity of GCA is detected in terms of recurrence.

Secondary Outcome Measures
NameTimeMethod
Correlation with clinical parameters2 years

Correlation of the measured tracer activity with clinically and laboratory-chemically available parameters that are collected in clinical routine. These include CRP, peripheral blood leukocyte count, calprotectin, serum amyloid A, haptoglobin and Lactate dehydrogenase and their respective progression.

Correlation with blood leukocyte count2 years

Correlation of tracer uptake on imaging with CXCR4-positive peripheral blood leukocyte count.

Comparison to other imaging modalities2 years

Comparison with imaging findings from vasculitis MRI imaging implemented in standard clinical practice, duplex sonography (CCDS), and, if performed as part of routine clinical practice, FDG PET/CT data.

Trial Locations

Locations (1)

Departement of Internal Medicine II, Rheumatology/Clinical Immunology

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Würzburg, Bayern, Germany

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