e15011 Background: Actionable gene fusions such as ALK, ROS1, and NTRK define critical therapeutic subsets across solid tumors but suffer from the needle-in-a-haystack challenge due to extreme rarity in unselected populations. We hypothesized that those fusion-driven oncogenesis imprints subtle and detectable morphological patterns on routine H RET: 307; ROS1: 255; and NTRK: 107). Model operating points were selected to support conservative pre-screening use, prioritizing high specificity and enrichment of fusion-positive cases. External validation was conducted on independent cohorts, including the TCGA Pan-Cancer Atlas, to assess generalizability across cancer types and domains. Results: PathMoE-Fusion, demonstrated robust pre-screening performance across multiple actionable gene fusion targets, achieving AUROC values ranging from 0.84 (ROS1) to 0.94 (NTRK). Crucially, when deployed as a pre-screening tool under a conservative operating point prioritizing high specificity, the model yielded positive predictive values of 80.2% for ALK and 70.2% for NTRK, indicating marked enrichment of fusion-positive cases relative to their baseline prevalence. In TCGA validation, PathMoE-Fusion showed improved pre-screening performance, with more favorable enrichment characteristics than baseline approaches. Conclusions: PathMoE-Fusion serves as a rapid, low-cost digital enrichment biomarker that transforms the search for rare gene fusions. By prioritizing specificity, it acts as a pre-screening filter to populate a high-yield queue for confirmatory DNA/RNA sequencing. This framework maximizes the cost-effectiveness of molecular diagnostics, ensuring that sequencing resources are concentrated on patients most likely to benefit from life-extending targeted therapies.
Ji et al. (Thu,) studied this question.