Progress in precision oncology, including biomarker discovery and individualized treatment selection, is limited by the complexity of clinico-genomic data and the scarcity of large multimodal patient cohorts. Here, we introduce PanoraOnc, a pan-cancer artificial intelligence (AI) model pretrained on real-world clinical, genomic, and imaging data from 84,131 patients spanning 66 cancer types. PanoraOnc enables transferable treatment outcome prediction through pan-cancer pretraining and generalizes to unseen cohorts across cancer types, institutions, and therapeutic settings. Evaluation and fine-tuning were performed on cohorts comprising diverse modalities, including clinical features, targeted gene panels, immunofluorescence imaging, whole-exome sequencing, and transcriptomic profiles. Across these settings, PanoraOnc consistently outperforms statistical, machine-learning, survival, and AI baselines, with the largest improvements observed in zero- and few-shot scenarios, demonstrating that large-scale clinico-genomic pretraining enables robust and generalizable outcome predictions across previously unseen conditions. In addition, PanoraOnc supports biomarker discovery through explainable AI, revealing both established and underappreciated features, including tumor-infiltrating clonal hematopoiesis, oncogenic signaling pathways, and DNA damage response mechanisms in immunotherapy-treated melanoma and non-small cell lung cancer. Furthermore, PanoraOnc enables the identification of patient subgroups potentially benefitting from alternative treatments by estimating personalized treatment outcomes across therapeutic scenarios. These findings establish pan-cancer multimodal pretraining as a scalable paradigm for AI-assisted discovery in precision oncology.
M. Schuerch, J. Geisberg, C. T. Flower et al.· medRxiv· 0 citations
Dysregulation of intracellular signaling networks underpins cancer. Yet, resolving signaling networks within distinct or rare cell types in cancer in vivo has been unattainable. Here we develop INSIGHT by integrating cell sorting with mass spectrometry to enable quantitative phosphoproteomics and proteomics of discrete cell types from fixed tissues. Using INSIGHT, we map the signaling network within disseminating glioblastoma cells from patient-derived xenografts implanted in mice. Disseminating tumor cells undergo a proteome-wide shift from proliferative to mesenchymal, neural progenitor-like cell states. In parallel, signaling network and global kinase activity are rewired, transitioning from cell cycle-associated circuitries to those governing synaptic function, neuronal migration, and ion channel activity. Changes begin at the tumor margin and persist in distant brain parenchyma. Hornerin and phosphorylation of Ca²⁺-permeable GluA2 at Y876 were identified as mediators of glioblastoma progression. INSIGHT enables systems-level dissection of cell-type-specific signaling circuitries in vivo across wide range of biological systems.
Ryuhjin Ahn, Alicia D’Souza, L. Long et al.· Nature Communications· 0 citations