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. 2025 Jul 29;15(1):27703.
doi: 10.1038/s41598-025-12428-2.

Building a dynamic web calculator for individualized conditional survival estimation in brainstem ependymoma

Affiliations

Building a dynamic web calculator for individualized conditional survival estimation in brainstem ependymoma

Hua Huang et al. Sci Rep. .

Abstract

Brainstem ependymomas (EPNs) are rare and aggressive central nervous system tumors with unique anatomical challenges and poor prognosis. Traditional survival estimates offer limited clinical guidance due to their static nature. This study aimed to investigate the dynamic survival patterns of brainstem EPNs using conditional survival (CS) analysis and to develop a web-based nomogram model for individualized, real-time prognostication. Patients diagnosed with primary brainstem EPNs between 2000 and 2021 were identified from the SEER database. CS analysis was performed to assess changes in survival probability over time. Annual hazard rates were calculated to identify high-risk periods. Prognostic variables were selected using best subset regression (BSR) and least absolute shrinkage and selection operator (LASSO) methods. A CS-based nomogram was constructed using multivariable Cox regression and validated through calibration plots, ROC curves, and decision curve analysis (DCA). A risk stratification system and an interactive web calculator were also developed. A total of 697 patients were included and randomly assigned to training (n = 487) and validation (n = 210) cohorts. CS analysis showed that as patients survive longer after diagnosis, their probability of surviving additional years increases steadily. And six variables (age, sex, race, histology, surgery, and radiotherapy) were identified via the LASSO model for nomogram construction. The CS-nomogram demonstrated good calibration and acceptable discrimination, with 1-, 3-, and 5-year AUCs of 0.626, 0.649, and 0.656 in the training cohort, and 0.688, 0.692, and 0.687 in the validation cohort, respectively. DCA confirmed the clinical utility of the model. A risk classification system effectively stratified patients into high- and low-risk groups with significantly different survival outcomes. A web-based calculator was created to facilitate real-world application. This study presents a novel CS-based nomogram that dynamically predicts survival in patients with brainstem EPNs. By capturing time-dependent survival probabilities and integrating key clinical factors, the model offers a practical tool to support individualized prognosis, patient counseling, and follow-up planning in clinical practice. While it offers individualized prognostic insights, its clinical use requires further external validation.

Keywords: Brainstem ependymomas; Conditional survival; Nomogram; Prognosis prediction; SEER.

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Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests. Conflict of interest: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Fig. 1
Fig. 1
Conditional survival analysis (A) and annual hazard rate analysis (B) for individuals diagnosed with ependymoma (EPN). Overall survival at initial diagnosis (time 0) and conditional survival for those who lived 1 to 4 years beyond diagnosis were assessed using the Kaplan-Meier method.
Fig. 2
Fig. 2
Predictive variable selection was performed using the best subset regression (BSR), and the least absolute shrinkage and selection operator (LASSO) techniques to optimize model tuning.
Fig. 3
Fig. 3
The performance of the LASSO and BSR models was compared using the area under the receiver operating characteristic curve (AUC).
Fig. 4
Fig. 4
A prognostic nomogram model was constructed based on conditional survival data to estimate individualized survival probabilities. EPN, ependymoma; RT, radiotherapy.
Fig. 5
Fig. 5
Assessment and validation of the conditional survival-driven nomogram included calibration curves (A and B) and time-dependent ROC analyses (C and D), evaluating model calibration and discriminative ability across both training and validation cohorts.
Fig. 6
Fig. 6
Decision curve analysis (DCA) was applied to determine the clinical benefit of the established nomogram for predicting outcomes in both training (A) and validation (B) groups.
Fig. 7
Fig. 7
Patients were grouped into distinct risk categories using a stratification system derived from the total score calculated by the conditional survival-based nomogram. (A) Distribution of risk scores; Kaplan-Meier survival curves and log-rank comparisons in the training (B) and validation (C) datasets.
Fig. 8
Fig. 8
A web-based risk calculator based on CS-nomogram model (https://seercancer.shinyapps.io/SEEREPN/). CS, conditional survival.

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