About this trial
This phase II trial studies whether different imaging techniques can provide additional and more accurate information than the usual approach for assessing the activity of tumors in patients with newly diagnosed glioblastoma. The usual approach for this currently is magnetic resonance imaging (MRI). This study is trying to learn more about the meaning of changes in MRI scans after treatment, as while the appearance of some of these changes may reflect progressing tumor, some may be due the treatment. Dynamic susceptibility contrast (DSC)-MRIs, along with positron emission tomography (PET) and/or magnetic resonance (MR) spectroscopy, may help doctors tell which changes are a reflection of the treatment and which changes may be due to progressing tumor.
Eligibility criteria
Qualifiers
Patient must be ≥ 18 years of age.
Patient must have a Karnofsky Performance Status ≥ 60%.
Patient must have newly diagnosed GBM (must be IDH wild type), with pathologic proof, based on World Health Organization (WHO) 2021 criteria.
Patient must be planning to receive standard-of-care treatment for newly diagnosed glioblastoma.
Disqualifiers
None
Trial design
Treatments tested in this trial
- Dynamic Susceptibility Contrast-Enhanced Magnetic Resonance Imaging
- Fluciclovine F18
- Gadolinium-Chelate
- Magnetic Resonance Spectroscopy
- Positron Emission Tomography
Treatment groups
Sponsors and collaborators
ECOG-ACRIN Cancer Research Group
Lead sponsor
National Cancer Institute (NCI)
Collaborator