Liver cancer is a leading cause of cancer mortality; hepatocellular carcinoma (HCC), its predominant form, requires accurate survival prediction to guide prognosis and treatment decisions. We propose a multimodal framework for discrete-time survival prediction using histopathological and clinical data from the TCGA-LIHC cohort. Patch-level features extracted from Whole-Slide Images using the UNI2-h foundation model were aggregated within each slide through a Graph Attention Network, while clinical variables were encoded with a sentence transformer. The resulting embeddings were fused through intermediate fusion strategies and processed by a multi-layer perceptron trained using a negative discrete-time log-likelihood loss to handle censored data. Across two clinically meaningful survival intervals, [0, 1) and [1, 5] years, multimodal fusion outperformed unimodal baselines, with concatenation achieving the highest overall performance (AUROC = 0.818). These findings highlight the complementary prognostic value of histology and clinical data for robust and interpretable survival modeling in HCC.
Multimodal Graph-Based Model for Discrete-Time Survival Prediction in Liver Cancer
Akebli H.;della Mea V.;Roitero K.
2026-01-01
Abstract
Liver cancer is a leading cause of cancer mortality; hepatocellular carcinoma (HCC), its predominant form, requires accurate survival prediction to guide prognosis and treatment decisions. We propose a multimodal framework for discrete-time survival prediction using histopathological and clinical data from the TCGA-LIHC cohort. Patch-level features extracted from Whole-Slide Images using the UNI2-h foundation model were aggregated within each slide through a Graph Attention Network, while clinical variables were encoded with a sentence transformer. The resulting embeddings were fused through intermediate fusion strategies and processed by a multi-layer perceptron trained using a negative discrete-time log-likelihood loss to handle censored data. Across two clinically meaningful survival intervals, [0, 1) and [1, 5] years, multimodal fusion outperformed unimodal baselines, with concatenation achieving the highest overall performance (AUROC = 0.818). These findings highlight the complementary prognostic value of histology and clinical data for robust and interpretable survival modeling in HCC.| File | Dimensione | Formato | |
|---|---|---|---|
|
SHTI-336-SHTI260182.pdf
accesso aperto
Tipologia:
Versione Editoriale (PDF)
Licenza:
Creative commons
Dimensione
385.41 kB
Formato
Adobe PDF
|
385.41 kB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


