abdominal neoplasms
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. There is no age limit, male or female; 2. The research object is clinically suspected or diagnosed tumor patients; 3. Participants who have completed 18F-FDG and 68Ga-FAPI-04 PET/CT scans; 4. There is at least one measurable target lesion according to RECIST1.1; 5. Participants who are able to provide informed consent (signed by the participant, parent or legal representative) and consent in accordance with the guidelines of the Clinical Research Ethics Committee.
Exclusion criteria
Exclusion criteria: 1. Serious abnormality of liver and kidney function; 2. Pregnant women, pregnant women and lactating women; 3. Those who cannot lie flat for half an hour; 4. Suffering from claustrophobia or other mental illness; 5. Treatment has started between PET scans; 6. Other investigators think that it is not suitable to participate in the trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Standard uptake value max;Standard uptake value mean; | — |
Countries
China
Contacts
The First Affiliated Hospital of Naval Medical University