About this trial
The objective of the study is to construct a noninvasive approach using 68Ga-labeled bicyclic peptide radiotracer to detect the matrix metalloproteinase 14 (MMP14, MT1-MMP) expression of tumor lesions in patients with solid tumors and to identify patients benefiting from MMP14 targeting treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Malignant melanoma, glioma, lung cancer, colon cancer, pancreatic cancer, gastric cancer, breast cancer, liver cancer, etc., confirmed by histopathology or cytology;
age ≥18 and ≤75 years old, male or female;
ECOG score 0 or 1;
expected survival time ≥6 months;
Disqualifiers
Pregnant or breastfeeding women, or women planning to become pregnant during the study or within three months after administration, as well as individuals donating sperm or oocytes.
Individuals known or suspected to be allergic to the investigational drug or any of its components.
Individuals with significantly abnormal liver or kidney function: serum total bilirubin (TBIL) > 1.5 × 20 µmol/L, or aspartate aminotransferase (AST) > 2.5 × 45 µmol/L, or alanine aminotransferase (ALT) > 2.5 × 40 µmol/L, or serum creatinine > 1.5 × 130 µmol/L.
Unable to cooperate in completing the PET scan, or suffering from claustrophobia or other conditions that prevent cooperation during the PET scan.
Trial population
Malignant tumor patients or suspected patients
Trial design
Case-only
Prospective
Treatments tested in this trial
18-FDG
DrugAll study participants will undergo one 18F-FDG PET/ CT scan.
Treatment groups
Trial outcomes
Primary outcomes
Standardized uptake value(SUV)
SUV is a semi-quantitative analysis index to describe the radioactive uptake of lesions, which has certain reference value for differentiating benign and malignant lesions. The uptake of the tracer (68Ga-MMP14) in solid tumor lesions by measuring SUV on PET/CT.
Sponsors and contacts
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