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Recruiting NCT05212272

MRI in High-Grade Glioma Patients Undergoing Chemoradiation

Trial Parameters

Condition High Grade Glioma
Sponsor Wake Forest University Health Sciences
Study Type INTERVENTIONAL
Phase N/A
Enrollment 16
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2022-09-02
Completion 2026-12
Interventions
PET-MRI Brain ScanBlood drawMemory testing

Brief Summary

The purpose of this research study is to see if investigators can predict how brain functioning changes after radiation treatment based on PET scans and blood tests. Most participants experience at least mild decreases in their memory or attention after radiation therapy. Investigators hope that PET scans, lumbar puncture, and blood tests might help investigators predict who might have larger changes in their brain function after radiation.

Eligibility Criteria

Inclusion Criteria: * Pathologically confirmed diagnosis of high-grade glioma (grade III or IV) or WHO grade II glioma, IDH wildtype (molecular glioblastoma multiforme \[GBM\]). * ≥18 years of age. * ECOG performance status of 0 to 3 * Anticipated to receive 6 weeks of chemoradiation Exclusion Criteria: * Does not speak or read English * Unable to participate in cognitive testing due to aphasia or other severe cognitive impairment as determined by the PI, or Dr. Cummings or her designee. * Unable to give informed consent * Past medical history of any kind of dementia or diagnosed with mild cognitive impairment prior to diagnosis with their brain tumor * Unable to safely fast for 8 hours prior to bloodwork or 6 hours prior to PET scan * Currently taking cognition-enhancing medications including: * Donepezil * Memantine * Armodafinil * Methylphenidate * Pregnant or nursing mothers. * Patients taking blood thinners will be excluded from the optional Lumbar Puncture only, they are eligible

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