Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05264688
Other study ID # 20220207
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 20, 2022
Est. completion date October 31, 2022

Study information

Verified date April 2022
Source Zhongnan Hospital
Contact Yufeng Yuan
Phone 13995564795
Email yuanyf1971@whu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients with high clinical suspicion of hepatobiliary malignancies should undergo PET/CT examination with two imaging agents, 68Ga-FAPI (fibroblast activation protein inhibitor) and 18F-FDG within one week, and collect tumor tissue. Finally, the PET/CT results were compared with the pathology report to evaluate the role of 68Ga-FAPI PET/CT imaging in the diagnosis of hepatobiliary malignancies


Description:

Patients with high clinical suspicion of hepatobiliary malignancies should undergo PET/CT examination with two imaging agents, 68Ga-FAPI (fibroblast activation protein inhibitor) and 18F-FDG within one week. After comprehensive clinical evaluation, if the patient can be treated with surgery, surgery will be performed, and the patient's pathological specimens will be collected after surgery ; If the patient has no possibility of surgery, ultrasound-guided needle biopsy is performed, and biopsy specimens are collected. Finally, the PET/CT results were compared with the pathology report to evaluate the application value of 68Ga-FAPI PET/CT imaging in the diagnosis and staging of hepatobiliary malignant tumors, and to analyze the guiding significance for the treatment decision of hepatobiliary malignant tumors.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date October 31, 2022
Est. primary completion date July 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Voluntarily participate and sign a written informed consent; 2. 18-80 years old (inclusive) male or female; 3. Patients with high clinical suspicion of hepatobiliary malignancy in combination with medical history and imaging studies, etc. 4. Those who obtained pathological diagnosis results through needle biopsy or surgical resection; 5. Have willingness and ability to participate in all research procedures. Exclusion Criteria: 1. Women who are pregnant or breastfeeding; 2. Those who are known to be allergic to the imaging agent 68Ga-FAPI or its excipients; 3. Those who have a history of other malignant tumors in the past; 4. Before the injection of 18F-FDG, the fasting blood glucose level exceeds 11.0mmol/L; 5. Patients with claustrophobia; 6. Those who cannot tolerate lying down for 15-30 minutes; 7. The researchers believe that it is not suitable to participate in this clinical trial; 8. Those who have participated in clinical trials or are participating in other clinical trials within the past month

Study Design


Intervention

Diagnostic Test:
68Ga-FAPI-04 imaging agent
1.85-3.7 MBq/kg body weight (0.05-0.1 mCi/kg) intravenously

Locations

Country Name City State
China Zhongnan Hospital Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Zhongnan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary diagnose accordance rate Proportion of PET/CT diagnostic reports consistent with pathological results 2022.1.20-2022.7.30
Secondary Standardized Uptake Mean (SUVmean) The average of the standard uptake value 2022.1.20-2022.7.30
Secondary Standardized Uptake Maximum (SUVmax) The maximum value of the standard uptake value 2022.1.20-2022.7.30
Secondary Tumor Background Ratio The ratio of the radiation concentration in the tumor area to the surrounding background 2022.1.20-2022.7.30
Secondary Tumor Metabolic Volume (MTV) The metabolically active volume of tumor tissue 2022.1.20-2022.7.30
Secondary Total Glycolysis (TLG) Tumor metabolic volume is multiplied by the mean of standard uptake 2022.1.20-2022.7.30
See also
  Status Clinical Trial Phase
Terminated NCT01200082 - Sulfation of Bile Acids as a Biomarker for Hepatobiliary Diseases