68Ga-FAPI-PSMA PET Imaging for the Diagnosis of Solid Tumors

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorPeking University Cancer Hospital & Institute

About this trial

This study aims to evaluate a novel dual-targeted PET imaging tracer, 68Ga-FAPI-PSMA, for the detection and evaluation of solid tumors. Fibroblast activation protein (FAP) and prostate-specific membrane antigen (PSMA) are two important molecular targets that are highly expressed in tumor cells or the tumor microenvironment. Combining these two targets into a single imaging probe may improve the sensitivity and accuracy of tumor detection.

In this single-center, open-label, self-controlled study, approximately 20 patients with suspected or confirmed solid tumors will undergo PET/CT imaging using 68Ga-FAPI-PSMA. The imaging results will be compared with standard PET tracers such as 68Ga-PSMA-617 or 68Ga-FAPI-04. The study will assess tracer uptake in tumor lesions and compare diagnostic performance between imaging methods. The results may help determine whether 68Ga-FAPI-PSMA PET/CT can improve tumor detection, staging, and clinical evaluation in patients with solid tumors.

Eligibility criteria

Qualifiers

Age 18-75 years

Patients with suspected or confirmed solid tumors (e.g., prostate cancer, hepatocellular carcinoma, ovarian cancer, or endometrial cancer)

Patients scheduled to undergo tumor biopsy or surgical treatment within 2 months

ECOG performance status of 0 or 1

Disqualifiers

Severe hepatic or renal dysfunction

Inability to remain in a supine position for approximately 30 minutes during PET/CT scanning

Refusal or inability to participate in the clinical study

Claustrophobia or severe psychiatric disorders that would interfere with imaging procedures

Trial design

Treatments tested in this trial

  • 68Ga-FAPI-PSMA
  • 68Ga-PSMA-617
  • 68Ga-FAPI-04

Treatment groups

20 Participants
are divided into 1 treatment group

Locations

This trial has no locations