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| Main Authors: | , , , , , , , , , |
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| Format: | Preprint |
| Published: |
2025
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2512.20633 |
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| _version_ | 1866912786418761728 |
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| author | Lee, MunHwan Chowdhury, Shaika Li, Xiaodi Rajaganapathy, Sivaraman Klee, Eric W Yang, Ping Sio, Terence Wang, Liewei Cerhan, James Zong, Nansu NA |
| author_facet | Lee, MunHwan Chowdhury, Shaika Li, Xiaodi Rajaganapathy, Sivaraman Klee, Eric W Yang, Ping Sio, Terence Wang, Liewei Cerhan, James Zong, Nansu NA |
| contents | Accurate prediction of treatment outcomes in lung cancer remains challenging due to the sparsity, heterogeneity, and contextual overload of real-world electronic health data. Traditional models often fail to capture semantic information across multimodal streams, while large-scale fine-tuning approaches are impractical in clinical workflows. We introduce a framework that uses Large Language Models (LLMs) as Goal-oriented Knowledge Curators (GKC) to convert laboratory, genomic, and medication data into high-fidelity, task-aligned features. Unlike generic embeddings, GKC produces representations tailored to the prediction objective and operates as an offline preprocessing step that integrates naturally into hospital informatics pipelines. Using a lung cancer cohort (N=184), we benchmarked GKC against expert-engineered features, direct text embeddings, and an end-to-end transformer. Our approach achieved a mean AUROC of 0.803 (95% CI: 0.799-0.807) and outperformed all baselines. An ablation study further confirmed the complementary value of combining all three modalities. These results show that the quality of semantic representation is a key determinant of predictive accuracy in sparse clinical data settings. By reframing LLMs as knowledge curation engines rather than black-box predictors, this work demonstrates a scalable, interpretable, and workflow-compatible pathway for advancing AI-driven decision support in oncology. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2512_20633 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Enhancing Lung Cancer Treatment Outcome Prediction through Semantic Feature Engineering Using Large Language Models Lee, MunHwan Chowdhury, Shaika Li, Xiaodi Rajaganapathy, Sivaraman Klee, Eric W Yang, Ping Sio, Terence Wang, Liewei Cerhan, James Zong, Nansu NA Machine Learning Artificial Intelligence Accurate prediction of treatment outcomes in lung cancer remains challenging due to the sparsity, heterogeneity, and contextual overload of real-world electronic health data. Traditional models often fail to capture semantic information across multimodal streams, while large-scale fine-tuning approaches are impractical in clinical workflows. We introduce a framework that uses Large Language Models (LLMs) as Goal-oriented Knowledge Curators (GKC) to convert laboratory, genomic, and medication data into high-fidelity, task-aligned features. Unlike generic embeddings, GKC produces representations tailored to the prediction objective and operates as an offline preprocessing step that integrates naturally into hospital informatics pipelines. Using a lung cancer cohort (N=184), we benchmarked GKC against expert-engineered features, direct text embeddings, and an end-to-end transformer. Our approach achieved a mean AUROC of 0.803 (95% CI: 0.799-0.807) and outperformed all baselines. An ablation study further confirmed the complementary value of combining all three modalities. These results show that the quality of semantic representation is a key determinant of predictive accuracy in sparse clinical data settings. By reframing LLMs as knowledge curation engines rather than black-box predictors, this work demonstrates a scalable, interpretable, and workflow-compatible pathway for advancing AI-driven decision support in oncology. |
| title | Enhancing Lung Cancer Treatment Outcome Prediction through Semantic Feature Engineering Using Large Language Models |
| topic | Machine Learning Artificial Intelligence |
| url | https://arxiv.org/abs/2512.20633 |