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Updated: Sep 7, 2026

Competing-Risk Nomogram for Predicting Cancer-Specific Survival in Multiple Primary Colorectal Cancer Patients after Surgery
Published on: September 27, 2024
Web-based dynamic nomogram for forecasting overall survival and cancer-specific survival among individuals with lymph
Zheyuan Wang1, Lu Zhang2, Zengyou Li3
1Department of General Surgery, The Second Hospital of Lanzhou University, Lanzhou, Gansu, China.
Background:
This study aimed to develop and validate prognostic models for Lymph Node (LN)-negative pancreatic cancer patients.
Methods:
Data were extracted from the SEER database (2004‒2015). The included participants were randomly divided into training (70%) and validation (30%) sets. Independent prognostic factors for Overall Survival (OS) and Cancer-Specific Survival (CSS) were identified using Cox and Fine-Gray models to construct predictive nomograms for 1-, 3-, and 5-year outcomes.
Results:
Among 5970 included patients, 4270 deaths occurred. The nomogram for OS included 11 variables and the nomogram for CSS included 10. For OS, the C-indices in the training and validation cohorts were 0.740 (95% CI 0.722-0.758) and 0.740 (95% CI 0.712-0.768), respectively. Similarly, the C-indices for CSS were 0.737 (95% CI 0.719-0.756) and 0.736 (95% CI 0.708-0.764), respectively. The AUCs for 1-, 3-, and 5-year OS were 0.794 (95% CI 0.770-0.818), 0.819 (95% CI 0.800-0.839), and 0.836 (95% CI: 0.816-0.855). Meanwhile, the AUCs for 1-, 3-, and 5-year CSS were 0.796 (95% CI: 0.781-0.812), 0.829 (95% CI: 0.816-0.841), and 0.850 (95% CI: 0.838-0.862), indicating strong predictive performance. Calibration curves confirmed good accuracy. Competing risk analysis showed conventional methods overestimated CSS, supporting the accuracy of the Fine-Gray model.
Conclusion:
We developed and internally validated two clinically practical nomograms for OS and CSS for patients with LN-negative pancreatic cancer. These models show favorable discrimination and calibration, enabling clinical risk stratification and prognosis assessment. Future external validation using independent cohorts is needed to confirm the generalizability of these models.
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