Overview
This clinical trial studies whether T2 star (T2\*) magnetic resonance imaging (MRI) and biomarker blood testing can help predict how World Health Organization (WHO) grade IV gliomas (malignant gliomas) might change or progress over time.
Description
This clinical trial studies whether T2 star (T2\) magnetic resonance imaging (MRI) and biomarker blood testing can help predict how World Health Organization (WHO) grade IV gliomas (malignant gliomas) might change or progress over time. WHO grade IV gliomas are the most common primary brain tumors. Despite aggressive standard of care treatment, overall survival remains low. Early identification of whether the glioma comes back after a period of improvement (recurrence) remains an important part of treatment management. Early identification of recurrence can be complicated as treatment effects can cause inflammation, making it difficult to identify recurrence on standard MRI. It has been shown that WHO grade IV gliomas have increased iron content and that as the glioma is treated, markers in the blood that represent iron related cell death (biomarkers) increase. T2\ mapping is an MRI technique routinely used to assess iron content within tissues and may help identify recurrence of the glioma on the MRI. The biomarker blood test in this study checks the levels of iron-related cell death biomarkers in the blood, which may help predict how well patients are responding to treatment. T2\* MRI and biomarker blood testing may be an effective way to predict how malignant gliomas might change or progress over time.
Eligibility
Inclusion Criteria:
- Age \> 21 years
- New pathologically confirmed diagnosis of WHO grade IV malignant glioma
- KPS \> 60
- Ability to give informed consent for standard of care chemotherapy and radiation therapy on the MR Linac and to study procedures for the protocol
Exclusion Criteria:
- History of previous malignancy other than non-melanoma skin cancer in the previous 5 years
- History of iron metabolic disorder such as hemochromatosis
- Inability to undergo MR studies due to size, claustrophobia, or metal implants or devices


