Endoplasmic reticulum stress-related cancer-associated fibroblasts (ERS-CAF) remodel the tumor microenvironment and drive immune exclusion and therapy resistance in chordoma, yet routine and non-invasive readouts of this biology are lacking. We hypothesized that standard pre-operative MRI and H&E whole-slide images (WSI) encode image-based surrogates of ERS-CAF-driven immunoregulation that can be learned and generalized across cancers. Three bulk-transcriptomic reference scores were defined for surrogate supervision, capturing ERS-program activity, ERS-CAF-immuneligand-receptor crosstalk and microenvironmental heterogeneity. In 126 chordoma cases, a stage-wise multimodal framework integrating calibrated WSI attention, gated radiopathomic fusion and domain alignment showed strong concordance with molecular profiles, independent prognostic value and biologically specific localization to fibrotic immune-excluded regions. These associations were generalized in zero-shot analyses to the TCGA pan-cancer. An MRI-only distilled model preserved most predictive performance with substantial gains in efficiency, supporting scalable non-invasive clinical application.
Zheng et al. (Fri,) studied this question.