CNS Brain Metastases, Esophageal Cancer, Head and Neck Cancer, Lung Cancer, Prostate Cancer
Conditions
Brief summary
Hypoxia is a key factor in malignant progression of a neoplasm. It is our aim to explore the basis for quantitative in vivo tumor imaging by Cu-61 diacetyl-bis(N4-methylthiosemicarbazone)PET imaging as a surrogate of tissue hypoxia. We hypothesize that the hypoxia levels are predictive of the tumor response to therapy. Patients will have 2 CU-ATSM PET scans done and the goal is to show spatially stable tracer distributions that correlate with tumor hypoxia. This study will serve as a pilot study for a PO1 submission
Interventions
imaging with CuATSM
Imaging with CuATSM
Imaging with CuATSM
imaging with CuATSM
Imaging with CuATSM
Sponsors
Study design
Eligibility
Inclusion criteria
* Able to tolerated a PET/CT scan * Age 18 or older * Patient being considered for XRT for treatment of their cancer * Able to provide written informed consent
Exclusion criteria
* severe claustrophobia or inability to tolerate the PET scan * pregnant or breastfeeding women * Patients that need supplemental oxygen * Patients enrolled in experimental treatments
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To validate the CuATSM-PET imaging by correlation to the serum level of osteopontin, a marker of hypoxia | end of study |
Secondary
| Measure | Time frame |
|---|---|
| To test reliability of the CuATSM uptake by quantifying the reproducibility of the pre-treatment CuATSM_PET scans | end of study |
| To assess the technical and logistic feasibility of CuATSM-PET scans in a population of cancer patients | end of study |
Countries
United States