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CXCR4-PET/CT for Diagnosing Giant Cell Arteritis

Detection of Disease Activity in Giant Cell Arteritis Using CXCR4-PET/CT

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05604482
Enrollment
10
Registered
2022-11-03
Start date
2021-10-01
Completion date
2023-09-30
Last updated
2023-12-15

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

Conditions

Diagnoses Disease, Vasculitis

Keywords

Vasculitis, LV-GCA, Giant cell arteritis, FDG-PET, Imaging, CXCR4

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.

Interventions

DIAGNOSTIC_TESTCXCR4-PET

New imaging modality using CXCR4 for imaging in GCA

Sponsors

Matthias Fröhlich
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Maximum measurable tracer activity on 68Ga-Pentixafor PET/CT in the area of blood vessels in active GCA2 yearsdetection 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

MeasureTime frameDescription
Correlation with clinical parameters2 yearsCorrelation 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 yearsCorrelation of tracer uptake on imaging with CXCR4-positive peripheral blood leukocyte count.
Comparison to other imaging modalities2 yearsComparison 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.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026