Skip to content

The Value of 68Ga-FAPI PET/CT in the Efficacy Evaluation of Advanced Unresectable Hepatocellular Carcinoma Patients Undergoing Systemic Antitumor Therapy

The Value of 68Ga-FAPI PET/CT in the Efficacy Evaluation of Advanced Unresectable Hepatocellular Carcinoma Patients Undergoing Systemic Antitumor Therapy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06746194
Enrollment
40
Registered
2024-12-24
Start date
2024-12-03
Completion date
2028-12-31
Last updated
2024-12-24

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

Conditions

Hepatocellular Carcinoma (HCC)

Keywords

hepatocellular carcinoma, 68Ga-FAPI, PET/CT

Brief summary

This study aims to investigate the value of 68Ga-FAPI PET/CT in the efficacy evaluation of advanced unresectable hepatocellular carcinoma patients undergoing systemic antitumor therapy.

Detailed description

The investigators will number all participants, create a medical record file, and record their basic information (gender, age) as well as contact information and medical history information. All participants will undergo a 68Ga-FAPI PET/CT before treatment and after 3-month treatment. The imaging response measurements will be compared with the histopathological results as gold standard.

Interventions

None listed

Sponsors

Ruijin Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Pathological and clinical diagnosis of advanced unresectable hepatocellular carcinoma patients. 2. Signed and dated informed consent form. 3. Commitment to comply with research procedures and co-operation in the implementation of the full research process. 4. Aged 18-75 years old.

Exclusion criteria

1. Patients with serious illnesses that researchers consider unsuitable for participation in this clinical study. Such as severe heart and lung failure, severe bone marrow suppression, severe liver and kidney dysfunction, etc. 2. Intestinal perforation, complete intestinal obstruction 3. Pregnant women and women who may be pregnant, women who are breastfeeding. 4. Non-compliant person

Design outcomes

Primary

MeasureTime frameDescription
The responses to systemic antitumor therapy of advanced unresectable hepatocellular carcinomaWithin 1 week of enrollment and up to 3 monthsThe tumor lesions were evaluated within one week of enrollment and at 3 months of treatment, and a comparison was made before and after. Those with improved tumor lesions were considered to have responded to the treatment, while those without improved tumor lesions were considered to have no response to the treatment.
Standardized uptake value(SUV)Within 1 week of enrollment and after up to 3 monthsSUV of 68Ga-FAPI uptake on PET/CT images for tumor lesions

Secondary

MeasureTime frameDescription
Progress free survival3 yearsProgress free survival
Overall survival3 yearsOverall survival

Countries

China

Contacts

Primary ContactJiajia Hu
jiajiahu@shsmu.edu.cn13524945287

Outcome results

None listed

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