A Prospective Study on the Diagnosis of Malignant Tumors With 18F-FGIn PET/CT

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorAffiliated Cancer Hospital & Institute of Guangzhou Medical University

About this trial

Glutamine is a crucial nutrient for cancer cell growth, and its metabolism is frequently dysregulated in malignancies. 18F-FGln is a PET tracer that targets this altered glutamine metabolism. However, there are currently limited studies on the diagnostic value of 18F-FGln PET/CT in various types of cancer. Therefore, this prospective study was conducted to investigate the value of 18F-FGln PET/CT in patients with various types of malignant tumors.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with clinical suspicion or exclusion of primary or recurrent malignant tumors (such as glioma of the brain, liver cancer, gastric cancer, duodenal cancer, colorectal cancer, ovarian cancer, etc., where 18F-FDG is prone to false negatives and false positives)

Patients undergoing tumor staging or evaluating treatment effect using 18F-FDG PET/CT or 18F-FGln PET/CT to determine the most appropriate treatment strategy

Patients without other tumor history

Patients with good compliance, providing informed consent, and able to follow the research protocol

Disqualifiers

pregnant or lactating patients or patients under 18 years old

the subjects and their parents or legal representatives are unable or unwilling to provide written informed consent;

patients with poor compliance, unable to tolerate or cooperate with PET/CT examinations.

those who have undergone gastrointestinal barium meal examination within one week;

Trial population

This study will include patients from the Affiliated Cancer Hospital \& Institute of Guangzhou Medical University who underwent an 18F-FGln PET/CT scan between October 2025 and January 2028 . Eligible participants are adult patients aged 18 to 70 years with suspected or histopathologically confirmed malignant tumors. Patients with non-malignant lesions, pregnant women, and those with incomplete medical records or missing histopathological reference standards will be excluded. Data will be collected by reviewing the institutional medical records and PET/CT imaging database.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

110 Participants
are grouped into 1 trial group
Group A: Patients with Malignant Tumors

Trial outcomes

Primary outcomes

1

SUVMAX

Xingxiang's Chinese report system automatically delineates the areas of interest.

Time frame
Within one day after the PET/CT scan
2

TBR

Xingxiang's Chinese report system automatically delineates the areas of interest.

Time frame
Within one day after the PET/CT scan

Secondary outcomes

Other outcomes

Sponsors and contacts

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