Patients with known or suspected primary or metastatic breast cancer with one lesion that is 1.0 cm in diameter or greater may be eligible for this study. Patients may participate in this study if they are at least 18 years of age. Up to 40 evaluable subjects will participate in a single imaging cohort. Patients will be stratified for analysis by breast cancer subtype with prioritization to recruit at least 10 estrogen-receptor-expressing (ER+) and 10 triple-negative breast cancers (TNBC). Participants may be treatment naïve or have received up to 3 weeks of treatment at the time of the \[18F\]F-Gln PET/CT scan. This is an observational study; \[18F\]F-GLN PET/CT will not be used to direct treatment decisions. While patients and referring physicians will not be blinded to the \[18F\]F-GLN PET/CT results, treatment decisions are made by the treating physicians based upon clinical criteria. \[18F\]F-GLN PET/CT imaging sessions will include an injection of \[18F\]F-GLN. Metabolism data will be collected. Pilot data will be collected to evaluate image quality and collect preliminary information on the uptake of \[18F\]F-GLN in breast cancer. Uptake measures will be compared to tumor markers of glutamine metabolism, when tissue is available. The safety of \[18F\]F-GLN will also be evaluated in all subjects.
Up to 40 patients will undergo approximately 60 minutes of dynamic PET scanning followed by up to 2 static skull-base to mid-thigh scans post injection of \[18F\] (2S,4R)4-fluoroglutamine (\[18F\]F-GLN). A baseline FDG-PET/CT will also be performed, either as a routine clinical staging/re-staging scan or as a research scan. If performed as a research scan, the scan may include an optional dynamic imaging session. Some subjects, who undergo systemic therapy as part of their clinical treatment, may also undergo an optional second \[18F\]F-GLN PET/CT to collect pilot data on the changes in \[18F\]F-GLN uptake in response to therapy. Subjects who undergo a second \[18F\]F-GLN PET/CT may have a second FDG-PET/CT, again either as a standard-of-care restaging study or as an optional research scan. The timing of the optional second PET scans will vary depending on the type of treatment the subject is receiving. If the subject moves during their scans, a low-dose CT attenuation may be repeated following the dynamic scan at the PI's discretion.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
40
Evaluate the kinetics and biodistribution of \[18F\]F-GLN in primary and metastatic breast cancer.
University of Pennsylvania
Philadelphia, Pennsylvania, United States
RECRUITINGKinetics and Biodistribution of [18F]F-GLN
Evaluate the biodistribution of \[18F\]F-GLN by measuring organ and whole body dosimetry.
Time frame: 3 years
Incidence of Adverse Events (Safety and Tolerability)
Evaluate the safety of \[18F\]F-GLN. Number of participants with treatment-related adverse events as assessed by CTCAE v4.0.
Time frame: 3 years
Association of Uptake with [18F]F-GLN
Assess the correlation of \[18F\]F-GLN with pathologic sub-types of breast cancer using standard pathology results, ER, PR, HER2.
Time frame: 3 years
Association with Tumor Markers and [18F]F-GLN
Correlate uptake of \[18F\]F-GLN with pathologic measurement of glutamine metabolism in tissue.
Time frame: 3 years
Metabolism of [18F]F-GLN
Measure the biometabolites in patient blood over time, following injection of \[18F\]F-GLN to determine the rate at which \[18F\]F-GLN is metabolized.
Time frame: 3 years
Change in Uptake of [18F]F-GLN After Therapy
Evaluate change in \[18F\]F-GLN uptake measures after therapy compared to pre-treatment baseline.
Time frame: 3 years
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