Using MRI scans to personalize radiotherapy for high grade glioma
Official title: Serial Advanced Magnetic Resonance Imaging (MRI) for Guidance of Personalized Adaptive Radiotherapy for High Grade Glioma
Run by M.D. Anderson Cancer Center · NCT04771806 · Data updated 2026-11-12
This study tests if using regular MRI scans to track tumor changes can help doctors personalize radiation treatment for patients with high grade glioma to improve their outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Drugs / interventions | chemotherapy, radiation |
| Locations | 1 site (Houston, Texas) |
| Status | Recruiting |
| Started | April 1, 2019 |
| Main results expected | February 2, 2027 |
| Study ends | February 2, 2027 |
| Registry record updated | September 14, 2026 |
| Trial ID | NCT04771806 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older with histologically confirmed high grade glioma and a Karnofsky performance status of 60 or higher.
✕Probably not a fit
Patients who are unable to undergo MRI scans or have lower performance status may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the effectiveness of repeated magnetic resonance imaging (MRI) scans in monitoring tumor changes during radiation and chemotherapy for patients with high grade glioma. It aims to compare the dosimetric coverage of the tumor using immediate post-operative MRI versus newly acquired MRI before radiation therapy. Additionally, the study evaluates the relationship between MRI findings and tumor progression, neurocognitive function, and overall survival. By adapting treatment plans based on serial MRI data, the study seeks to improve patient outcomes.
Why it matters
Potential benefit: If successful, this approach could lead to more personalized and effective treatment plans for patients with high grade glioma.
How similar studies have gone: Other studies have shown promise in using adaptive radiotherapy approaches, but this specific methodology is novel in its focus on serial MRI for high grade glioma.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * All patients with histologic confirmation of high grade glioma * Patients must be age \>= 18 years * Patients must sign informed consent indicating that they are aware of the investigational nature of this study in keeping with the policies of the hospital. The only acceptable consent form is the one attached at the end of this protocol, and has been approved and amended by the MD Anderson Cancer Center (MDACC) Institutional Review Board (IRB) * Patients must have Karnofsky performance status (KPS) \>= 60 * Patients must be able to obtain an MRI scan with gadolinium contrast * Female patients of childbearing age must not be pregnant as determined with a serum beta human chorionic gonadotropin (HCG) no greater than 14 days prior to study registration, or breastfeeding. (The exclusion is made because gadolinium may be teratogenic in pregnancy). Female patients who consent to participate in the study will need to use contraceptive methods for the duration of the study
Where it's running
-
M D Anderson Cancer Center
Houston, Texas, United States Recruiting
Study contacts
- Principal investigator: Caroline Chung — M.D. Anderson Cancer Center
- Study coordinator: Caroline Chung
- Email: cchung3@mdanderson.org
- Phone: 713-563-2300
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.