A novel structural modeling magnitude and orientation radiomic descriptor for evaluating response to neoadjuvant therapy in rectal cancers via MRI.
Publication Title
NPJ Precis Oncol
Document Type
Article
Publication Date
7-1-2025
Keywords
oregon; chiles
Abstract
With advances in neoadjuvant therapies for rectal cancer, accurately evaluating tumor regression and response is increasingly critical for enabling personalized follow-up, including non-operative management. Given the lack of reliable assessment methods, there is an opportunity to develop computerized image-based markers for identifying early responders. We present a novel radiomic signature, the STructural mOdeling magnituDE and Orientation (StODeO) descriptor for quantifying image-based surrogates of tumor shrinkage within and around the rectum via routine MRI scans. StODeO descriptors measure both the magnitude (how much) and direction (inward/outward) of structural displacements in the diseased rectal wall, with respect to a newly constructed, first-of-its-kind image-based reference atlas of the non-diseased rectum. Combined with traditional radiomic texture features, StODeO showed superior performance in distinguishing pathologic response groups of rectal cancer patients post-chemoradiation (hold-out validation AUC 0.77) as well as segregating composite response groups in a clinical trial of immune checkpoint inhibitors (external validation accuracy 0.71; NCT02688712). The integrated StODeO-texture signature demonstrated robustness across annotation sources and imaging variations, intuitive modeling of therapy-associated structural changes, and statistical associations with tumor-immune biology, including macrophages and CD8+ T-cells from multiplexed biopsy analysis. StODeO offers a novel image-based surrogate of tissue displacements from treatment effects and residual disease after neoadjuvant therapy in rectal cancers.
Area of Special Interest
Cancer
Area of Special Interest
Digestive Health
Specialty/Research Institute
Oncology
Specialty/Research Institute
Gastroenterology
DOI
10.1038/s41698-025-01007-3