About this trial
The US FDA approved a targeted somatostatin receptor 2 imaging agent, 68Ga-DOTATATE, in 2016. It has higher uptake in small cell lung cancer, pulmonary carcinoid, and medullary thyroid cancer. Integrin αvβ3 is highly expressed in some tumor cells and new blood vessels, making it an ideal target for targeted diagnosis and treatment of tumors and tumor vessels.68Ga-labeled DOTA-TATE-RGD is a new type of tumor-specific imaging agent developed by researchers based on the above foundation, which is used for targeted diagnosis and internal radiation therapy for patients with SSTR2 and αvβ3 positive tumors.
Eligibility criteria
Qualifiers
histologically confirmed various cancer patients;
68Ga-TATE-RGD and 18F-FDG PET/CT within a week;
signed written consent.
Disqualifiers
known allergy against TATE-RGD;
any medical condition that in the opinion of the investigator may significantly interfere with study compliance.
Trial design
Treatments tested in this trial
- 68Ga-TATE-RGD
- 18-FDG