Detection in Progress - A Multimodal Segmentation-based Approach for Predicting Glioblastoma Recurrence
Abstract
Radiation therapy planning for patients with glioblastoma requires defining the clinical-target-volume by delineating the tumor and including a margin of healthy tissue to account for microscopic tumor spread post radiation therapy. The current standard-of-care practice for defining the clinical-target-volume still employs an isotropic 1–2 cm expansion of the identified T2-hyperintensity lesion. As a consequence, normal-appearing brain tissue is overtreated, and it also ends up missing progression regions as it overlooks the heterogeneous infiltrative nature of these tumors. We propose incorporating anatomical, metabolic, and diffusion-weighted imaging acquired before surgical resection or between surgery and radiation therapy, using a lesion-size-aware segmentation objective to improve clinical-target-volume definition. The results in multiple metrics demonstrate better prediction of tumor progression than standard of care, as indicated by contrast enhancement and T2-hyperintensity at recurrence. Overall, our approach minimizes treatment of normal-appearing brain and captures progressed voxels beyond the 2 cm expansion.