Learning from Limited and Incomplete Data: A Multimodal Framework for Predicting Pathological Response in NSCLC
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Abstract (arXiv)
Major pathological response (pR) following neoadjuvant therapy is a clinically meaningful endpoint in non-small cell lung cancer, strongly associated with improved survival. However, accurate preoperative prediction of pR remains challenging, particularly in real-world clinical settings characterized by limited data availability and incomplete clinical profiles. In this study, we propose a multimodal deep learning framework designed to address these constraints by integrating foundation model-based CT feature extraction with a missing-aware architecture for clinical variables. This approach enables robust learning from small cohorts while explicitly modeling missing clinical information, without relying on conventional imputation strategies. A weighted fusion mechanism is employed to leverage the complementary contributions of imaging and clinical modalities, yielding a multimodal model that consistently outperforms both unimodal imaging and clinical baselines. These findings underscore the added value of integrating heterogeneous data sources and highlight the potential of multimodal, missing-aware systems to support pR prediction under realistic clinical conditions.
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References · 6
- 2023On the Challenges and Perspectives of Foundation Models for Medical Image Analysiscited by 135
- 2024A Systematic Review of Intermediate Fusion in Multimodal Deep Learning for Biomedical Applicationscited by 25
- 2024Not Another Imputation Method: A Transformer-based Model for Missing Values in Tabular Datasetscited by 10
- 2025Doctor-in-the-Loop: An Explainable, Multi-View Deep Learning Framework for Predicting Pathological Response in Non-Small Cell Lung Cancercited by 7
- 2024MARIA: a Multimodal Transformer Model for Incomplete Healthcare Datacited by 5
- 2025Multimodal Doctor-in-the-Loop: A Clinically-Guided Explainable Framework for Predicting Pathological Response in Non-Small Cell Lung Cancercited by 2
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