Data-Efficient and Explainable Multimodal Survival Prediction in NSCLC Using Deep Image Embeddings, Clinical Variables, and Gradient-Boosted Trees
Data-Efficient and Explainable Multimodal Survival Prediction in NSCLC Using Deep Image Embeddings, Clinical Variables, and Gradient-Boosted Trees
Abstract
Background/Objectives: Survival prediction in non-small cell lung cancer (NSCLC) remains challenging, particularly in limited-sample settings where end-to-end deep learning models may suffer from limited generalization. This study aimed to develop a data-efficient, multimodal, and explainable framework integrating computed tomography (CT)-derived imaging information with clinical variables for NSCLC survival prediction. Methods: CT images, tumor segmentations, and clinical data from the publicly available NSCLC Radiomics (LUNG1) dataset (377 patients) were used. Tumor-focused regions were extracted using segmentation masks, and pretrained RadImageNet-InceptionV3 embeddings were obtained from the largest tumor-containing slice and neighboring-slice summaries. Deep imaging embeddings, engineered imaging features, and clinical variables were fused into a unified tabular representation. To improve robustness under limited-sample conditions, feature blocks were compressed using principal component analysis. CatBoost, XGBoost, and LightGBM models were trained on a development set and evaluated on a strictly held-out final validation set. Results: In three-class survival stratification, assigning censored/non-event patients to the upper survival group produced the strongest ordinal prognostic performance. Under the EX_PLUS_NON_EX_TOP setting, CatBoost achieved the best holdout score-based class C-index of 0.655. In continuous survival regression, LightGBM achieved the best holdout event-patient C-index of 0.576. Clinical variables provided the dominant prognostic signal, while compact deep image embeddings contributed complementary information, particularly in separating short- and long-survival groups. SHAP analysis confirmed contributions from both clinical and image-derived features. Conclusions: The proposed framework provides a proof-of-concept demonstration of a data-efficient and explainable image-to-tabular approach for NSCLC survival prediction under strict internal holdout validation. The results suggest that pretrained CT embeddings, clinical variables, gradient-boosted trees, and SHAP-based interpretation can be combined in a feasible, limited-sample survival modeling pipeline, while external validation remains necessary before clinical translation.
Description
Keywords
CT Radiomics, Small Datasets, Survival Prediction, Explainable AI, Multimodal Learning, Artificial Intelligence, Radiomics, Deep Learning, Pattern Recognition (Psychology), NSCLC, Gradient-Boosted Trees, Robustness (Evolution), Deep Image Embeddings
Fields of Science
Citation
WoS Q
Scopus Q
Source
Volume
16
Issue
12
Start Page
1941
End Page
1941

