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(68)Ga-FAPI PET/CT in Patients With ANCA-associated Vasculitis

Application Value of Novel PET Tracers Targeting CAF in ANCA-Associated Vasculitis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07151521
Acronym
GFPIPWAAV
Enrollment
30
Registered
2025-09-03
Start date
2025-09-01
Completion date
2028-07-01
Last updated
2025-11-17

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

Conditions

ANCA-associated Vasculitis

Keywords

ANCA-associated vasculitis, FAPI, PET/CT, ILD, Kidney

Brief summary

Pulmonary and renal involvement are the most common clinical manifestations of antineutrophil cytoplasmic antibody(ANCA)-associated vasculitis (AAV). Studies have shown that both interstitial lung disease (ILD) and renal dysfunction are closely associated with poor prognosis in patients with AAV. Therefore, early identification of whether AAV patients have concomitant ILD and renal involvement is of great clinical importance for assessing disease severity, stratifying prognostic risk, and developing individualized treatment strategies. Positron emission tomography (PET) is a noninvasive molecular imaging technique that can provide decision-making support for early and accurate diagnosis, timely intervention, as well as evaluation of treatment response and prognosis. In the same individual, PET enables whole-body localization of disease in a single examination, overcoming the limitation of conventional diagnostic methods that typically assess only one region at a time, thereby facilitating patient benefit. In recent years, many novel PET tracers have been developed and introduced into clinical practice. 68Ga-Fibroblast Activation Protein Inhibitor (FAPI) has been studied in the diagnosis of various malignant and nonmalignant diseases; it targets fibroblast activation protein (FAP) and thus reflects the distribution of cancer-associated fibroblasts (CAFs). However, its clinical significance in AAV remains to be further investigated. This study aims to use a CAF-targeted novel PET tracer to conveniently and noninvasively detect the real-time distribution of lesions in patients, providing valuable information for personalized diagnosis and treatment.

Interventions

None listed

Sponsors

Ruijin Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. Age over 18 years; 2. Meeting the 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR) classification criteria for ANCA-associated vasculitis; 3. Diagnosed with concomitant interstitial lung disease based on High-Resolution Computed Tomography (HRCT) images obtained within one year prior to enrollment, interpreted by two radiologists blinded to clinical information; 4. Complete clinical information available; 5. Signed and dated informed consent form; 6. Willingness to comply with the study procedures and cooperate throughout the entire study process.

Exclusion criteria

1. Presence of other rheumatic diseases; 2. Presence of other conditions that may cause interstitial lung disease or renal impairment, such as systemic lupus erythematosus, dermatomyositis, or rheumatoid arthritis; 3. History of, or planned, hematopoietic stem cell transplantation; 4. Presence of severe comorbidities deemed by the investigators to be unsuitable for participation in this clinical study, such as severe cardiopulmonary insufficiency, severe bone marrow suppression, or severe hepatic or renal insufficiency; 5. Acute abdominal emergencies such as intestinal perforation or complete intestinal obstruction; 6. Pregnant or potentially pregnant women, and lactating women; 7. Poor treatment compliance.

Design outcomes

Primary

MeasureTime frame
Disease severity and activity in ANCA-associated vasculitis with concomitant interstitial lung disease and renal dysfunction as measured by 68Ga-FAPI PET/CT.Within 4 weeks after enrollment

Countries

China

Contacts

Primary ContactHong-Lei Liu
hong-lei-liu@163.com+8617721375702
Backup ContactJiajia Hu
hjj11592@rjh.com.cn+8613524945287

Outcome results

None listed

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