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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04514614
Other study ID # PekingUMCHFAPIRA
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date September 1, 2020
Est. completion date December 1, 2022

Study information

Verified date January 2021
Source Peking Union Medical College Hospital
Contact Yaping Luo, MD
Phone 86-10-69155513
Email luoyaping@live.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

68Ga-FAPI has been developed as a tumor-targeting agent as fibroblast activation protein is overexpressed in cancer-associated fibroblasts and some inflammation, such as IgG4-related disease and inflammatory bowel disease. Some researches identified FAP expression in synovial samples taken from both rheumatoid arthritis and osteoarthritis patients.Thus this prospective study is going to investigate whether 68Ga-FAPI PET/CT may be superior for diagnosis, therapy response assessment and follow-up of arthritis than 18F-FDG PET/CT.


Description:

Arthritis is a term used to mean any disorder that affects the joints. The two most common forms of arthritis are osteoarthritis and rheumatoid arthritis.Rheumatoid arthritis is an autoimmune chronic inflammatory disease of unknown etiology and is characterized by chronic inflammation of the joint capsule's synovial membrane. This chronic inflammation ultimately destroys the underlying cartilage and bone. Activated fibroblast-like synoviocytes (FLS) line the synovial membrane and are a prominent cell type responsible for inflammation and joint destruction. Osteoarthritis is characterized by degradation of joint cartilage. Studies demonstrate chondrocytes expressed FAP and that chondrocyte FAP expression was elevated in patients with osteoarthritis. Other researches identified FAP expression in synovial samples taken from both rheumatoid arthritis and osteoarthritis patients. However, FAP expression was greater in samples taken from refractory rheumatoid arthritis patients in comparison to end-stage osteoarthritis patients.68Ga-FAPI has been developed as a tumor-targeting agent as fibroblast activation protein is overexpressed in cancer-associated fibroblasts and some inflammation, such as IgG4-related disease and inflammatory bowel disease. Recently the investigators have published an article of the application of 68Ga-FAPI in IgG4-related disease which showed it was more sensitive than FDG in detecting a certain type of inflammations. Thus this prospective study is going to investigate whether 68Ga-FAPI PET/CT may be superior for diagnosis, therapy response assessment and follow-up of arthritis than 18F-FDG PET/CT.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 1, 2022
Est. primary completion date January 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - suspected or confirmed untreated arthritis patients; - 18F-FDG PET/CT within two weeks; - signed written consent. Exclusion Criteria: - pregnancy; - breastfeeding; - known allergy against FAPI - any medical condition that in the opinion of the investigator may significantly interfere with study compliance.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
68Ga-FAPI
Intravenous injection of one dosage of 74-148 MBq (2-4 mCi) 68Ga-FAPI. Tracer doses of 68Ga-FAPI will be used to image lesions of arthritis by PET/CT.

Locations

Country Name City State
China Peking Union Medical College Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic value Sensitivity and Specificity of 68Ga-FAPI PET/CT for IgG4-RD in comparison with 18F-FDG PET/CT. through study completion, an average of 1 year
Secondary Metabolic parameters Total Lesion Glycolysis (TLG) of focal lesions are measured on 68Ga-FAPI PET/CT. Time Frame: through study completion, an average of 1 year
Secondary Disease burden assessement whether Total Lesion Glycolysis (TLG) assessed on 68Ga-FAPI PET/CT was correlated with clinical parameters for arthritis using correlation coefficients analysis through study completion, an average of 1 year
Secondary FAPI expression and SUV Correlation between FAPI expression and SUV in PET through study completion, an average of 1 year
Secondary Therapy response Change of Total Lesion Glycolysis (TLG) on 68Ga-FAPI PET/CT after therapy through study completion, an average of 1 year
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