AUTHOR=Yang Zichen , Zhao Shouxiang , Cheng Zhenting , Ge Dengfeng , Ren Hao , Xu Jiankang , Zhang Bin TITLE=Combined inflammatory-lipid index and tumor markers for predicting the spatial localization of lesions in early-stage non-small cell lung cancer JOURNAL=Frontiers in Oncology VOLUME=Volume 15 - 2025 YEAR=2025 URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2025.1635315 DOI=10.3389/fonc.2025.1635315 ISSN=2234-943X ABSTRACT=ObjectiveThis study evaluated the predictive value of combined inflammatory-lipid indices and tumor markers in determining lesion localization in early-stage non-small cell lung cancer (NSCLC) and developed a predictive model.MethodsA retrospective analysis of 206 early-stage NSCLC patients was conducted from December 1, 2023, to September 30, 2024. Patients were grouped based on tumor location: upper lobe and lower lobe. Significant predictors were identified through univariate and multivariate logistic regression analyses, leading to the development of a nomogram. Predictive performance was assessed using the receiver operating characteristic (ROC) curve and area under the curve (AUC). Model calibration was evaluated with a calibration plot, and decision curve analysis (DCA) was utilized to assess the model’s relevance in clinical settings.ResultsAmong the 206 patients, 135 (65.53%) had upper lobe tumors, and 71 (34.47%) had lower lobe tumors. Significant differences were found in white blood cell (WBC) count, lymphocyte count, α-hydroxybutyrate dehydrogenase (α-HBDH), high density lipoprotein cholesterol (HDL) triglycerides, low-density lipoprotein cholesterol (LDL), total cholesterol, carcinoembryonic antigen (CEA), serum ferritin (SF), carbohydrate antigen 125 (CA125), carbohydrate antigen 153 (CA153), and carbohydrate antigen 199 (CA199) (all p < 0.05). Multivariate logistic regression identified WBC (OR: 1.46, 95% CI: 1.13–1.95, p = 0.007), a-HBDH (OR: 1.01, 95% CI: 1.00–1.03, p = 0.041), HDL (OR: 7.08, 95% CI: 1.50–36.16, p = 0.015), CEA (OR: 1.12, 95% CI: 1.02–1.23, p = 0.021), SF (OR: 1.01, 95% CI: 1.00–1.02, p = 0.020), CA153 (OR: 1.08, 95% CI: 1.00–1.16, p = 0.037), and CA199 (OR: 1.16, 95% CI: 1.07–1.27, p < 0.001) as independent risk factors for lower lobe tumor localization. An AUC of 0.806 was obtained for the nomogram (95% CI: 0.743–0.868), indicating good calibration, and showed favorable clinical utility based on decision curve analysis (DCA).ConclusionWBC count, lymphocyte count, α-HBDH, HDL, CEA, SF, CA153, and CA199 are significant predictors of lesion localization in early-stage NSCLC. The developed nomogram, based on readily available clinical parameters, demonstrated strong predictive performance and may aid in individualized diagnosis and treatment planning. Further large-scale external validation is needed.