Malignant Glioma
Conditions
Keywords
malignant glioma, FDOPA, PET CT, radiation therapy
Brief summary
For most brain tumors, radiation treatment is guided by a Magnetic Resonance Imaging (MRI) scan. In this study, information from a special scan, called a Positron Emission Tomography/ Computed Tomography (PET/CT) scan using an amino acid called Fluorine-18-L-dihydroxyphenylalanine (18F-DOPA) will also be used. This type of scan has shown promise in being able to better distinguish tumor from normal brain tissue and may help to more accurately plan radiation treatment. This type of scan can also assist the radiation oncologist in identifying the most aggressive regions of the tumor. The goal of this study is to compare the 18F-DOPA PET/CT scan with the MRI scan for identifying where the disease is that needs to be treated with radiation.
Interventions
DRUGFluorine-18-L-dihydroxyphenylalanine
5 millicuries ± 10%; Intravenous injection; 1 time
Sponsors
Mayo Clinic
Brains Together for the Cure
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
7 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥7 years. * Biopsy confirmed newly diagnosed or recurrent WHO Grade II or Grade III malignant glioma. * CT simulation, 18F-DOPA PET imaging, and standard of care pre-radiotherapy MRI scans to be performed at Mayo Clinic Rochester. * Willing to sign release of information for any follow-up records. * Provide informed written consent.
Exclusion criteria
* Patients diagnosed with WHO grade IV malignant glioma. * Patients previously treated with radiation therapy. * Unable to undergo MRI scans with contrast (e.g. cardiac pacemaker, defibrillator, kidney failure). * Unable to undergo an 18F-DOPA PET scan (e.g. Parkinson's Disease, taking anti-dopaminergic, or dopamine agonist medication or less than 6 half-lives from discontinuance of dopamine agonists) * Pregnant women * Nursing women * Men or women of childbearing potential who are unwilling to employ adequate contraception
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Treatment volume comparison | 6 weeks | The primary endpoint for this pilot study will be to compare radiotherapy treatment volumes defined by conventional MR-only with treatment volumes defined with both 18F-DOPA PET and conventional MR information |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Advanced imaging volume comparison | 6 weeks | For patients who have advanced MRI scans performed as part of standard clinical care, advanced MRI volumes will be compared with conventional MRI volumes as well as 18F-DOPA PET volumes |
| Concordance with recurrence | up to 10 years | For patients who progress radiographically within the observation period of this study will compare concordance of recurrence locations with pre-treatment 18F-DOPA PET uptake |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORNadia N Laack, MD
Mayo Clinic
PRINCIPAL_INVESTIGATORDebra Brinkmann, PhD
Mayo Clinic
PRINCIPAL_INVESTIGATORDeanna Pafundi, PhD
Mayo Clinic
Outcome results
None listed