Actively Recruiting
Evaluation of 68Ga-SorB PETCT Imaging for Diagnosing Sortilin-Expressing Solid Tumors in Adults with Melanoma, Liver, Lung, Pancreatic, Breast, or Ovarian Cancer
Led by Peking University Third Hospital · Updated on 2026-08-12
50
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the safety, feasibility, and diagnostic accuracy of a new PET tracer called 68Ga-SorB targeting Sortilin, a receptor highly expressed in several solid tumors including melanoma, liver, lung, pancreatic, breast, and ovarian cancers. This exploratory diagnostic study compares 68Ga-SorB PETCT imaging to the standard 18F-FDG PETCT, aiming to improve tumor detection and characterization by using a more tumor-specific tracer with fewer false positives. Participants will receive a single intravenous dose of 68Ga-SorB followed by whole-body PETCT imaging about 60 minutes after injection. The study compares these imaging results with clinically indicated 18F-FDG PETCT scans done within a set timeframe. No therapeutic treatments are given as part of this study. Approximately 40 to 50 adults with confirmed or suspected tumors will be enrolled for imaging and follow-up. During the study, participants are monitored for adverse events from tracer administration until about 24 hours post-imaging. Tumor uptake is measured using quantitative PET parameters such as SUVmax and tumor-to-background ratio. Follow-up includes pathology review and clinical assessments up to 3 months after imaging to evaluate lesion detection, diagnostic sensitivity, specificity, and overall accuracy. This research will provide initial clinical evidence to support further development of Sortilin-targeted imaging and potential future therapeutic applications.
CONDITIONS
Brief Title
68Ga-SorB PET/CT Imaging in Patients With Solid Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 75 years
- Histologically confirmed or clinically suspected melanoma, hepatocellular carcinoma, lung cancer, breast cancer, pancreatic cancer, or ovarian cancer
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Adequate blood counts and organ function as defined by specified laboratory thresholds
- Normal cardiac function
- Estimated life expectancy of at least 12 weeks
- Willing and able to comply with study procedures and follow-up
- At least one measurable target lesion according to RECIST version 1.1
- Use of effective contraception during the study and for 3 months after imaging for participants of childbearing potential
- Clinically indicated to undergo 18F-FDG PET/CT for tumor evaluation
- Able to understand the study procedures and provide written informed consent
You will not qualify if you...
- Pregnant or breastfeeding women
- Severe dysfunction of major organs including heart, liver, or kidney judged as unsuitable by investigator
- Inability to tolerate PET/CT imaging or complete study follow-up
- Any other condition judged by the investigator to make the participant unsuitable for the study
Research Team
M
Meixin Zhao
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