Adaptive Radiotherapy and MRIs Based on Patients With Newly Diagnosed High-Grade Glioma
Running, not enrolling
Conditions studied: Glioblastoma, Anaplastic Astrocytoma, Astrocytoma, Anaplastic Oligodendroglioma
In brief
The purpose of this study is to find out if performing additional Magnetic Resonance Image (MRI) scans of the subjects' brain during each week of the radiation treatment of their high-grade glioma will help improve the radiation treatment.
Key facts
- Study ID
- NCT06108206
- Run by
- Columbia University
- People needed
- 20
- Starts
- 2024-01-30
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-04-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histopathologically proven diagnosis of glioblastoma, anaplastic astrocytoma, or anaplastic oligodendroglioma
- History and physical examination within 28 days prior to enrollment
- Karnofsky performance status 70 or greater
- Age 18 years or greater
- Negative pregnancy test for females of childbearing potential before 1st research MRI, performed in accordance to institutional guidelines.
- Plan to receive standard of care 59.4-60 Gy in 30-33 fractions of radiotherapy. Glioblastoma patients over 65 year-old can receive standard of care hypofractionated radiotherapy including 40 Gy in 15 fractions.
You may not qualify if…
- Prior therapy for tumor except for biopsy or resection, including prior radiotherapy to the brain.
- Clinical or radiological evidence of metastatic disease outside the brain
- Prior malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 2 years
Where it is running
- Columbia University Irving Medical Center/NYPH — New York, New York, United States
Full record on ClinicalTrials.gov
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