BACKGROUND: We aim to predict outcomes of human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC), a subtype of head and neck cancer characterized with improved clinical outcome and better response to therapy. Pathology and radiology focused AI-based prognostic models have been independently developed for OPSCC, but their integration incorporating both primary tumour (PT) and metastatic cervical lymph node (LN) remains unexamined. METHODS: We investigate the prognostic value of an AI approach termed the swintransformer-based multimodal and multi-region data fusion framework (SMuRF). SMuRF integrates features from CT corresponding to the PT and LN, as well as whole slide pathology images from the PT as a predictor of survival and tumour grade in HPV-associated OPSCC. SMuRF employs cross-modality and cross-region window based multi-head self-attention mechanisms to capture interactions between features across tumour habitats and image scales. FINDINGS: Developed and tested on a cohort of 277 patients with OPSCC with matched radiology and pathology images, SMuRF demonstrated strong performance (C-index = 0.81 for DFS prediction and AUC = 0.75 for tumour grade classification) and emerged as an independent prognostic biomarker for DFS (hazard ratio [HR] = 17, 95% confidence interval [CI], 4.9-58, p < 0.0001) and tumour grade (odds ratio [OR] = 3.7, 95% CI, 1.4-10.5, p = 0.01) controlling for other clinical variables (i.e., T-, N-stage, age, smoking, sex and treatment modalities). Importantly, SMuRF outperformed unimodal models derived from radiology or pathology alone. INTERPRETATION: Our findings underscore the potential of multimodal deep learning in accurately stratifying OPSCC risk, informing tailored treatment strategies and potentially refining existing treatment algorithms. FUNDING: The National Institutes of Health, the U.S. Department of Veterans Affairs and National Institute of Biomedical Imaging and Bioengineering.
No clinical trial protocols linked to this paper
Clinical trials are automatically linked when NCT numbers are found in the paper's title or abstract.PICO Elements
No PICO elements extracted yet. Click "Extract PICO" to analyze this paper.
Paper Details
MeSH Terms
Associated Data
No associated datasets or code repositories found for this paper.
Related Papers
Related paper suggestions will be available in future updates.