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Comparing Habitat, Radiomics, and Fusion Models for Predicting Micropapillary/Solid Components in Stage I Lung
Shaoyu Huang1, Xiuzhen Liang1, Kaihua Lou2
1Department of Radiology, The Affiliated Lihuili Hospital of Ningbo University, 315010 Ningbo, Zhejiang, PR China (S.H., X.L., J.Z., J.W., H.D.).
Academic Radiology
|August 1, 2025
Summary
A novel fusion model accurately predicts micropapillary/solid status in stage I lung adenocarcinoma. This advanced model integrates radiomics and habitat signatures for improved preoperative prediction of lung cancer subtypes.
Area of Science:
- Oncology
- Radiology
- Medical Imaging
Background:
- Lung adenocarcinoma (LAC) is a major cause of cancer mortality.
- Accurate preoperative prediction of tumor subtype, such as micropapillary/solid (MP/S) status, is crucial for treatment planning in stage I LAC.
Purpose of the Study:
- To compare the efficacy of habitat models (HM), radiomics models (RM), and fusion models (FM) for predicting MP/S status in stage I LAC.
- To develop and validate advanced predictive models using imaging features.
Main Methods:
- Retrospective analysis of 345 stage I LAC patients from two centers.
- Development of HM using K-means clustering and RM using CT images.
- Creation of feature-based pre-fusion (pre-FM) and decision-based post-fusion (post-FM) models.
- Evaluation of model performance using Area Under the Curve (AUC) and Integrated Discrimination Improvement (IDI).
Main Results:
- The habitat model showed superior performance over the radiomics model in the training cohort (AUC: 0.900 vs. 0.876).
- The pre-fusion model consistently outperformed both HM and RM across all cohorts.
- The post-fusion model achieved the highest AUCs (0.952 in training, 0.850 in internal validation) and significant IDI improvements (14.2%-36.4%).
Conclusions:
- The post-fusion model, integrating clustering signatures, radiomics signatures, and clinical characteristics, is a reliable predictor for MP/S status in stage I LAC.
- This fusion approach offers enhanced preoperative prediction capabilities for lung adenocarcinoma subtypes.

