This phase II trial tests how well 18F-fluciclovine works to identify patients with cancer that has spread to brain (metastasis). 18F-fluciclovine is a radioactive diagnostic agent that is injected into a patient and taken up by tumor cells. The cells can then be visualized using positron emission tomography (PET)/computed tomography (CT) imaging scans. This will assist with identifying tumor cell growth of brain tumor cells, assist in determining treatment, and indirectly overall survival.18F-fluciclovine PET/CT scans may help doctors provide early determination of tumor cell growth of brain tumors to hopefully affect treatment and indirectly overall survival.
Additional locations may be listed on ClinicalTrials.gov for NCT06055790.
Locations matching your search criteria
United States
Arizona
Tucson
Banner University Medical Center - TucsonStatus: Active
Contact: Bital Savir-Baruch
Phone: 520-621-9093
 PRIMARY OBJECTIVES: 
I. To characterize the dynamics of 18F-fluciclovine uptake within a metastatic brain lesion over 60 minutes (mins).
II. To assess the dynamics of 18F-fluciclovine uptake within recently treated metastatic brain lesions.
III. Evaluate the potential use of 18F-fluciclovine in delineating true local progression from radionecrosis in patients with clinical uncertainty of indeterminate magnetic resonance imaging (MRI).
EXPLORATORY OBJECTIVES: 
I. To characterize tumor perfusion with 18F-fluciclovine at 0-2 min post injection prior to therapy.
II. To characterize tumor perfusion with 18F-fluciclovine at 0-2 min post injection after therapy.
OUTLINE: 
Patients receive 18F-fluciclovine intravenously (IV). Patients undergo PET/CT over 60 minutes before standard of care radiation therapy and up to 7 days after post therapy magnetic resonance imaging (MRI). Patients may undergo a third 18F-fluciclovine PET/CT at disease progression.
After completion of study, patients are followed up to 3 years.
Lead OrganizationBanner University Medical Center - Tucson
Principal InvestigatorBital Savir-Baruch