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Updated: Jan 8, 2026

Establishing a Competing Risk Regression Nomogram Model for Survival Data
Published on: October 23, 2020
Development of a laboratory-based nomogram for predicting clinical outcomes in patients with severe COVID-19
Langqing Xu1, Chunyang Hou2, Jing Jie1
1Department of Respiratory Medicine, Center for Infectious Diseases and Pathogen Biology, State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, The First Hospital of Jilin University, Changchun, China.
Insights
High ferritin and IL-10 levels predict poor response to glucocorticoids in severe COVID-19 patients. A new nomogram integrating these biomarkers aids risk stratification for personalized treatment strategies.
Area of Science:
- Critical Care Medicine
- Immunology
- Infectious Diseases
Background:
- Glucocorticoids are standard for severe COVID-19, but outcomes vary significantly.
- Inflammatory markers may help predict treatment response and personalize care.
Purpose of the Study:
- To develop a predictive model for glucocorticoid treatment response in severe COVID-19.
- To integrate inflammatory biomarkers for improved risk stratification.
Main Methods:
- Retrospective analysis of 151 severe COVID-19 patients receiving glucocorticoids.
- LASSO and logistic regression identified predictors; ROC curves determined thresholds.
- A nomogram was built and validated using split-sample and cross-validation.
Main Results:
- Elevated ferritin (>970.7 ng/mL) and IL-10 (>4.79 pg/mL) predicted glucocorticoid resistance (AUC 0.779-0.780).
- The nomogram included diabetes, ferritin, and IL-10, showing good calibration and discrimination.
- Diabetes was associated with worse outcomes, potentially worsened by glucocorticoid-induced hyperglycemia.
Conclusions:
- A novel nomogram incorporating ferritin and IL-10 demonstrates predictive value for glucocorticoid response in severe COVID-19.
- This tool may facilitate risk stratification and personalized management.
- Prospective validation in larger cohorts is recommended.
Background:
While glucocorticoids remain cornerstone therapy for severe COVID-19, substantial heterogeneity persists in clinical outcomes. This single-center retrospective study sought to establish a predictive model integrating inflammatory biomarkers to guide risk stratification and personalized management.
Methods:
We analysed 151 adults with WHO-defined severe COVID-19 receiving glucocorticoid therapy (December 2022-August 2023). Treatment non-response was defined as mortality during hospitalization, mechanical ventilation escalation, or persistent organ dysfunction. LASSO and logistic regression analyses identified predictors, with optimal biomarker thresholds determined using ROC curves. A nomogram was constructed and validated via split-sample testing (7:3 ratio) and 10-fold cross-validation.
Results:
Ferritin >970.7 ng/mL and IL-10 > 4.79 pg./mL predicted glucocorticoid resistance (AUC: training set 0.779, test set 0.780). The nomogram incorporated diabetes, ferritin, and IL-10, demonstrating robust calibration (Hosmer-Lemeshow p = 0.84; Brier score = 0.182) and discrimination (sensitivity = 71.4%, specificity = 70.0%). Diabetic patients exhibited heightened inflammatory responses and poorer outcomes, exacerbated by glucocorticoid-induced hyperglycaemia.
Conclusion:
This nomogram shows promising predictive performance and provides a potentially implementable framework for risk stratification and personalized management, which warrants prospective validation in larger, multi-center cohorts.
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