MRI for Brain Tumor
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to determine if brain scans and blood tests can predict changes in memory or attention following radiation treatment for brain tumors. Researchers seek to identify whether these tests can pinpoint individuals likely to experience significant changes in brain function. The trial includes PET and MRI brain scans, a blood draw, and a memory test. Individuals with high-grade glioma, a type of brain tumor, who are about to begin six weeks of combined chemotherapy and radiation, may be suitable candidates. Participants should not have severe cognitive impairments or be taking medications that enhance cognition. As an unphased trial, this study provides a unique opportunity to contribute to research that could improve future brain tumor treatments.
Will I have to stop taking my current medications?
If you are currently taking cognition-enhancing medications like Donepezil, Memantine, Armodafinil, or Methylphenidate, you will need to stop taking them to participate in this trial. If you are on blood thinners, you can still join the main study but cannot participate in the optional lumbar puncture.
What prior data suggests that this protocol is safe for brain tumor patients?
Research has shown that PET-MRI is a promising tool for studying brain tumors, providing detailed images that enhance doctors' understanding. This combination of PET and MRI aids in both diagnosing and managing brain conditions.
Regarding safety, studies have examined the use of PET-MRI with the tracer 18F-fluciclovine in patients with severe brain tumors. These studies found it safe for managing brain tumors in children, indicating it is well-tolerated.
While the trial under consideration focuses on changes in brain function after radiation, studies have not identified major safety concerns with PET-MRI. This is important to consider when deciding whether to join the trial.12345Why are researchers excited about this trial?
This trial focuses on using PET-MRI scans to better understand high-grade gliomas, a type of aggressive brain tumor. Researchers are excited about this trial because combining PET and MRI scans offers a more detailed picture of the tumor's structure and activity than standard MRI or CT scans alone. This comprehensive imaging approach could lead to more accurate assessments of how the tumor is responding to chemoradiation, potentially improving personalized treatment plans. Additionally, by including memory testing and blood draws, researchers hope to gather valuable data on how these tumors and their treatments affect brain function and overall health.
What evidence suggests that this trial's methods could be effective for predicting brain function changes after radiation?
Research has shown that using both PET and MRI scans together can improve the diagnosis of brain tumors, such as high-grade gliomas. In this trial, participants will undergo PET-MRI scans, which studies have found to be slightly more effective at identifying these tumors than PET/CT scans. This combined method helps doctors see the tumor more clearly and might predict changes in brain function after treatments like radiation. PET scans use a special dye to show how organs function, while MRIs use magnets and radio waves to create detailed brain images. By combining these scans, doctors can gain a clearer view of brain activity, which is crucial for planning treatment.26789
Who Is on the Research Team?
Christina Cramer, MD
Principal Investigator
Wake Forest Baptist Comprehensive Cancer Center
Are You a Good Fit for This Trial?
This trial is for adults over 18 with high-grade glioma (grade III or IV) or specific grade II glioma, who are about to undergo 6 weeks of chemoradiation. They should be able to perform daily activities with varying degrees of assistance and must not have dementia, cognitive impairments before their tumor diagnosis, or be on cognition-enhancing drugs. Pregnant women and those unable to consent or fast before procedures are excluded.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Chemoradiation Treatment
Participants undergo chemoradiation treatment, including PET scans, MRI scans, blood draws, and memory testing
Follow-up
Participants are monitored for cognitive decline and changes in biomarkers post-treatment
What Are the Treatments Tested in This Trial?
Interventions
- N/A
Find a Clinic Near You
Who Is Running the Clinical Trial?
Wake Forest University Health Sciences
Lead Sponsor