Published January 1, 2026 | Version v1
Journal article Open

Machine learning-assisted classification of lung cancer: the role of sarcopenia, inflammatory biomarkers, and PET/CT anatomical-metabolic parameters

  • 1. Altinbas Univ, Vocat Sch Hlth Sci, Radiotherapy Program, Kartaltepe Dist 11, TR-34217 Istanbul, Turkiye
  • 2. Istanbul Training & Res Hosp, Dept Nucl Med, Cerrahpasa Org Abdurrahman Nafiz Gurman Cd 24, TR-34098 Istanbul, Turkiye
  • 3. Istanbul Univ, Sci Fac, Nucl Phys Dept, TR-34134 Istanbul, Turkiye
  • 4. Yedikule Chest Dis Hosp, Dept Nucl Med, TR-34020 Istanbul, Turkiye
  • 5. Istanbul Galata Univ, Vocat Sch, Physiotherapy Program, Evliya Celebi Dist,Mesrutiyet St 62, TR-34430 Istanbul, Turkiye
  • 6. Altinbas Univ, Fac Med, Dept Chest Dis, Bahcelievler Med Pk Hosp, E5 Highway,Kultur St 1, TR-34147 Istanbul, Turkiye
  • 7. Istanbul Bilgi Univ, Inst Grad Programs, Physiotherapy & Rehabil Master Program, Eyupsultan, TR-34060 Istanbul, Turkiye

Description

Accurate differentiation between non-cancerous, benign, and malignant lung cancer remains a diagnostic challenge due to overlapping clinical and imaging characteristics. This study proposes a multimodal machine learning (ML) framework integrating positron emission tomography/computed tomography (PET/CT) anatomic-metabolic parameters, sarcopenia markers, and inflammatory biomarkers to enhance classification performance in lung cancer. A retrospective dataset of 222 patients was analyzed, including demographic variables, functional and morphometric sarcopenia indices, hematological inflammation markers, and PET/CT derived parameters such as maximum and mean standardized uptake value (SUVmax, SUVmean), metabolic tumor volume (MTV), total lesion glycolysis (TLG). Five ML algorithms-Logistic Regression, Multi-Layer Perceptron, Support Vector Machine, Extreme Gradient Boosting, and Random Forest-were evaluated using standardized performance metrics. Synthetic Minority Oversampling Technique was applied to balance class distributions. Feature importance analysis was conducted using the optimal model, and classification was repeated using the top 15 features. Among the models, Random Forest demonstrated superior predictive performance with a test accuracy of 96%, precision, recall, and F1-score of 0.96, and an average AUC of 0.99. Feature importance analysis revealed SUVmax, SUVmean, total lesion glycolysis, and skeletal muscle index as leading predictors. A secondary classification using only the top 15 features yielded even higher test accuracy (97%). These findings underscore the potential of integrating metabolic imaging, physical function, and biochemical inflammation markers in a non-invasive ML-based diagnostic pipeline. The proposed framework demonstrates high accuracy and generalizability and may serve as an effective clinical decision support tool in early lung cancer diagnosis and risk stratification.

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