N-LODDS: A Novel Integrated Lymph Node Staging System Enhancing Prognostic Accuracy in Non-Small-Cell Lung Cancer.
TL;DR
The N-LODDS staging system significantly improves prognostic accuracy by integrating anatomical and quantitative lymph node features, providing a novel tool for personalized NSCLC management.
OpenAlex 토픽 ·
Lung Cancer Diagnosis and Treatment
Radiomics and Machine Learning in Medical Imaging
Hepatocellular Carcinoma Treatment and Prognosis
The N-LODDS staging system significantly improves prognostic accuracy by integrating anatomical and quantitative lymph node features, providing a novel tool for personalized NSCLC management.
- p-value P<0.001
APA
Qiying Chen, Meihong Yao, et al. (2026). N-LODDS: A Novel Integrated Lymph Node Staging System Enhancing Prognostic Accuracy in Non-Small-Cell Lung Cancer.. Annals of surgical oncology, 33(5), 4242-4255. https://doi.org/10.1245/s10434-025-19005-x
MLA
Qiying Chen, et al.. "N-LODDS: A Novel Integrated Lymph Node Staging System Enhancing Prognostic Accuracy in Non-Small-Cell Lung Cancer.." Annals of surgical oncology, vol. 33, no. 5, 2026, pp. 4242-4255.
PMID
41559465
Abstract
[BACKGROUND] This study aimed to develop and validate a novel lymph node staging system integrating anatomical location and quantitative characteristics, evaluate its prognostic prediction efficacy in non-small-cell lung cancer (NSCLC), and establish a multivariate prognostic model.
[METHODS] A total of 23,676 patients with NSCLC from the SEER database (2010-2015) were enrolled. Optimal cutoffs for lymph node parameters (NPLN, LNR, LODDS) were determined using X-tile software. Composite variables (N-NPLN, N-LNR, N-LODDS) were constructed by integrating N staging. Independent prognostic factors were screened via Cox regression, and a nomogram was developed. Performance was assessed using the receiver operating characteristic curves, calibration curves, and decision curve analysis.
[RESULTS] N-LODDS staging demonstrated optimal prognostic prediction, significantly outperforming N-LNR and N-NPLN. The nomogram incorporating N-LODDS, tumor size, and nine independent prognostic factors showed superior discrimination and calibration (5 year area under the curve 0.740; 95% confidence interval 0.731-0.749) in both training and validation cohorts, with significant advantages over the TNM staging system (all P<0.001).
[CONCLUSION] The N-LODDS staging system significantly improves prognostic accuracy by integrating anatomical and quantitative lymph node features, providing a novel tool for personalized NSCLC management. Future multicenter prospective studies are needed to validate its clinical utility.
[METHODS] A total of 23,676 patients with NSCLC from the SEER database (2010-2015) were enrolled. Optimal cutoffs for lymph node parameters (NPLN, LNR, LODDS) were determined using X-tile software. Composite variables (N-NPLN, N-LNR, N-LODDS) were constructed by integrating N staging. Independent prognostic factors were screened via Cox regression, and a nomogram was developed. Performance was assessed using the receiver operating characteristic curves, calibration curves, and decision curve analysis.
[RESULTS] N-LODDS staging demonstrated optimal prognostic prediction, significantly outperforming N-LNR and N-NPLN. The nomogram incorporating N-LODDS, tumor size, and nine independent prognostic factors showed superior discrimination and calibration (5 year area under the curve 0.740; 95% confidence interval 0.731-0.749) in both training and validation cohorts, with significant advantages over the TNM staging system (all P<0.001).
[CONCLUSION] The N-LODDS staging system significantly improves prognostic accuracy by integrating anatomical and quantitative lymph node features, providing a novel tool for personalized NSCLC management. Future multicenter prospective studies are needed to validate its clinical utility.
MeSH Terms
Humans; Carcinoma, Non-Small-Cell Lung; Lung Neoplasms; Female; Male; Neoplasm Staging; Nomograms; Prognosis; Middle Aged; Lymph Nodes; Aged; Survival Rate; Follow-Up Studies; Lymphatic Metastasis; ROC Curve; Carcinoma, Squamous Cell; SEER Program; Adenocarcinoma
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