5T4 Targeting Nanobody Probe for PET Imaging in Solid Tumors

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorPeking University Cancer Hospital & Institute

About this trial

This study aims to evaluate a novel 5T4 targeted nanobody PET imaging tracer, 68Ga-MY, for the detection and evaluation of solid tumors.

The 5T4 oncofoetal antigen is considered a valuable tumor-associated antigen, which is expressed in many different cancers, but is rarely expressed in normal adult tissues. And cell surface expression of 5T4 is an important property for antibody-targeted therapies. It has been shown that 5T4 is expressed on tumour-initiating cells (TICs) and associated with worse clinical outcome. Moreover, decreased adherence due to 5T4 expression may be associated with cancer spread.

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-MY. The imaging results will be compared with 18F-FDG. The study will assess tracer uptake in tumor lesions and compare diagnostic performance between imaging methods. The results may help determine whether 68Ga-MY PET/CT can improve tumor detection, staging, and clinical evaluation in patients with solid tumors.

Eligibility criteria

Qualifiers

Patients with solid tumors;

Presence of measurable lesions on imaging examinations;

Expected survival ≥12 weeks.

Disqualifiers

Severe hepatic or renal dysfunction;

Women who are planning pregnancy, pregnant, or breastfeeding;

Unable to remain in supine position for 30 minutes;

Refusal to participate in this clinical study;

Trial design

Treatments tested in this trial

  • 18F-FDG
  • 68Ga-MY

Treatment groups

20 Participants
are divided into 1 treatment group