Commun Med (Lond). 2025 Nov 20;5(1):487. doi: 10.1038/s43856-025-01177-y.
ABSTRACT
BACKGROUND: Glioblastoma is a malignant primary brain tumor. Because of its highly invasive and infiltrative nature, surgical resection and radiation therapy are not able to remove all tumor cells, even with state-of-the-art imaging and fluorescence-guided surgery.
METHODS: 24 newly diagnosed glioblastoma patients were enrolled. Pre- and post-surgery MRI scans were performed. Magnetic susceptibility was quantified based on gradient echo MRI. The ratio between sub-voxel paramagnetic and diamagnetic susceptibility components was computed. Relationships between the proposed ratio metric and prognostic factors and pathological iron were investigated. Perfusion and permeability imaging were used to exclude the presence of blood-related contribution to the paramagnetic component.
RESULTS: Here we show that by decomposing tissue magnetic susceptibility into paramagnetic and diamagnetic sources, we can identify, non-invasively and in vivo, areas of altered iron metabolism associated with tumor activities in the edema tissue surrounding glioblastoma. We find that the paramagnetic to diamagnetic susceptibility ratio uniquely delineates area of hyperintensity corresponding to a Tumor and Immune cells Infiltration Zone. Statistically significant relationships are found between the ratio metrics in the infiltration zone and tumor prognostic factors. Follow-up scans reveal tumor progression and later contrast-enhancement in the predicted infiltration zone. Histological data indicate that increased iron content causes the elevated ratio metric.
CONCLUSIONS: Our study proposes a method to derive an iron-related imaging marker of abnormal patterns in the edema region of the glioblastoma associated with tumor cell infiltration. We show the potential of the imaging marker to aid and improve surgical and treatment planning.
PMID:41266763 | DOI:10.1038/s43856-025-01177-y
