Independent Risk Factors and Nomogram-Based Prediction of Pulmonary Fungal Infection in Lung Cancer Inpatients: A Single-Center Retrospective Study

Yanran Xu,1,2 Yan Chen1,2 1Department of Respiratory and Critical Care Medicine, The Second Clinical Medical College of North Sichuan Medical College, Nanchong, Sichuan, 637000, People’s Republic of China; 2Department of Respiratory and Critical Care Medicine, Beijing Anzhen Nanchong Hospital of Capital Medical University & Nanchong Central Hospital, Nanchong, Sichuan, 637000, People’s Republic of ChinaCorrespondence: Yan Chen, Email [email protected]: To investigate independent risk factors and construct an internally validated risk prediction model for invasive pulmonary fungal infection (IPFI) in patients with lung cancer.Patients and Methods: Clinical data from 250 consecutive lung cancer inpatients admitted to Nanchong Central Hospital between February 2022 and March 2025 were retrospectively analyzed; 41 patients developed IPFI and 209 did not. Patients were randomly assigned to a training set (n=175) and a validation set (n=75) at a 7:3 ratio. Candidate predictors were screened by univariate logistic regression, reduced using least absolute shrinkage and selection operator (LASSO) regression with 10-fold cross-validation, and entered into multivariable logistic regression to construct a nomogram. Model performance was evaluated using bootstrap internal validation (1000 resamples), calibration curves and goodness-of-fit testing, receiver operating characteristic analysis, and decision curve analysis.Results: Diabetes mellitus, invasive procedures, systemic glucocorticoid use, lower CD4+ T-cell count, and length of hospital stay > 14 days were associated with IPFI and were retained as independent predictors in the final model. The model showed good discrimination, with an area under the curve of 0.876 (95% CI: 0.809– 0.944) in the training set and 0.861 (95% CI: 0.750– 0.973) in the validation set, and demonstrated clinical net benefit across threshold probability ranges of 0.03– 0.90 (training) and 0.04– 0.78 (validation).Conclusion: This nomogram may support early risk stratification for IPFI among lung cancer inpatients, while confirmation in external, multi-center cohorts is needed before broader clinical application.Keywords: lung cancer, invasive pulmonary fungal infection, risk factors, nomogram, prediction model

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Publication Details

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SHILAP Revista de lepidopterología
Published
2026-02-01
Primary Topic
Antifungal resistance and susceptibility
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article

Independent Risk Factors and Nomogram-Based Prediction of Pulmonary Fungal Infection in Lung Cancer Inpatients: A Single-Center Retrospective Study

Chen Y, Xu Y
SHILAP Revista de lepidopterología
Antifungal resistance and susceptibility
article

Independent Risk Factors and Nomogram-Based Prediction of Pulmonary Fungal Infection in Lung Cancer Inpatients: A Single-Center Retrospective Study

Chen Y, Xu Y
article en

Abstract

Yanran Xu,1,2 Yan Chen1,2 1Department of Respiratory and Critical Care Medicine, The Second Clinical Medical College of North Sichuan Medical College, Nanchong, Sichuan, 637000, People’s Republic of China; 2Department of Respiratory and Critical Care Medicine, Beijing Anzhen Nanchong Hospital of Capital Medical University & Nanchong Central Hospital, Nanchong, Sichuan, 637000, People’s Republic of ChinaCorrespondence: Yan Chen, Email [email protected]: To investigate independent risk factors and construct an internally validated risk prediction model for invasive pulmonary fungal infection (IPFI) in patients with lung cancer.Patients and Methods: Clinical data from 250 consecutive lung cancer inpatients admitted to Nanchong Central Hospital between February 2022 and March 2025 were retrospectively analyzed; 41 patients developed IPFI and 209 did not. Patients were randomly assigned to a training set (n=175) and a validation set (n=75) at a 7:3 ratio. Candidate predictors were screened by univariate logistic regression, reduced using least absolute shrinkage and selection operator (LASSO) regression with 10-fold cross-validation, and entered into multivariable logistic regression to construct a nomogram. Model performance was evaluated using bootstrap internal validation (1000 resamples), calibration curves and goodness-of-fit testing, receiver operating characteristic analysis, and decision curve analysis.Results: Diabetes mellitus, invasive procedures, systemic glucocorticoid use, lower CD4+ T-cell count, and length of hospital stay > 14 days were associated with IPFI and were retained as independent predictors in the final model. The model showed good discrimination, with an area under the curve of 0.876 (95% CI: 0.809– 0.944) in the training set and 0.861 (95% CI: 0.750– 0.973) in the validation set, and demonstrated clinical net benefit across threshold probability ranges of 0.03– 0.90 (training) and 0.04– 0.78 (validation).Conclusion: This nomogram may support early risk stratification for IPFI among lung cancer inpatients, while confirmation in external, multi-center cohorts is needed before broader clinical application.Keywords: lung cancer, invasive pulmonary fungal infection, risk factors, nomogram, prediction model

SHILAP Revista de lepidopterología
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Antifungal resistance and susceptibility
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