Assessing 11C-Choline (11C-CH) PET to Distinguish True Tumor Progression From Pseudoprogression in High-grade Gliomas
Brain Cancer
About this trial
This is an interventional diagnostic trial for Brain Cancer focused on measuring 11C-Choline (11C-CH) PET, 16-676, High-grade Gliomas
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years
- Patient is able to provide written informed consent prior to study registration
- Histologically-confirmed high-grade glioma
- Completion of treatment with standard radiation (with or without concurrent therapy).
- Standard gadolinium-enhanced MRI changes that are considered indeterminate for tumor progression vs. treatment-related changes by the neuroradiologist or clinician within 24 weeks of completion of radiation.
Exclusion Criteria:
- Inability to undergo or cooperate with an MRI or PET scan (e.g., claustrophobia, metal implant)
- Renal insufficiency with recent (<3 month old) creatinine > 2.0 mg/dL
- Pregnant or nursing female
Sites / Locations
- Memorial Sloan Kettering Cancer Center
Arms of the Study
Arm 1
Experimental
high-grade glioma
Eligible patients must have undergone standard radiation (typically 60Gy in 30 fractions), with or without concurrent drug therapy, and have MRI findings consistent with tumor progression and/or pseudoprogression within 24 weeks after completion of radiation. Eligible patients will undergo an 11C-CH PET study within 2 weeks of the standard of care MRI that shows changes concerning for tumor progression vs. pseudoprogression. All patients will then be followed with surveillance brain MRI with and without contrast as per standard of care for a period of 11 months, to assess further progression or stabilization of the lesion. Initial MRI changes are considered to represent pseudoprogression/treatment related changes if the lesion stabilizes or becomes smaller without a change in tumor-related therapy. Otherwise, it will be considered a recurrence should there be progessive radiographic changes.