Evidence map›Paper›PMID 42305501›Full record

ArticleTranslational cancer research2026

Personalized survival prediction in pediatric glioblastoma using a machine learning-powered web tool.

Shaohuai Chen, Regina Chizi Tunje, Anjie Lu, Xinyu Ji, Hansong Sheng, Xiangjie Kong

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Article in Translational cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Shaohuai Chen *Department of Neurosurgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Regina Chizi Tunje *Department of Neurosurgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Anjie Lu *Department of Neurosurgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Xinyu JiDepartment of Neurosurgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Hansong ShengDepartment of Neurosurgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.
Xiangjie KongDepartment of Neurosurgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pediatric glioblastoma (p-GBM) is a rare but highly aggressive malignancy with limited treatment options and persistently poor outcomes. Conventional survival estimates at diagnosis inadequately capture the evolving prognosis of long-term survivors. Conditional survival (CS) analysis provides a dynamic perspective but has rarely been applied to p-GBM. This study aimed to investigate incidence trends, evaluate dynamic CS patterns, and develop a CS-based nomogram for individualized prognostic prediction in p-GBM. Methods: Using the Surveillance, Epidemiology, and End Results (SEER) database [2000-2021], we identified 597 patients (≤18 years) with newly diagnosed GBM. Incidence trends were evaluated by Joinpoint regression. Overall survival (OS) and CS were assessed with Kaplan-Meier and Cox models. Prognostic determinants were identified using multivariable analysis and least absolute shrinkage and selection operator (LASSO) regression. A CS-based nomogram was developed, internally validated, and deployed as an interactive web tool for individualized prognostic estimation. Results: Incidence of p-GBM remained stable over two decades [annual percent change (APC) =1.52, P>0.05]. CS probabilities improved markedly with increasing survival time: the 5-year CS rose from 14% at diagnosis to 88% at four years post-diagnosis. Multivariable analysis identified infratentorial location, large tumor size, and disease extension as adverse prognostic factors, whereas gross total resection and chemotherapy conferred significant survival benefits. The CS-based nomogram, incorporating tumor site, extent, surgery, and chemotherapy identified through the LASSO analysis, exhibited robust calibration, moderate discrimination, and notable clinical utility. Moreover, risk stratification clearly differentiated high- from low-risk patients (P<0.001), while the web-based calculator enabled real-time, individualized CS estimation. Conclusions: This population-level study highlights the dynamic nature of prognosis in p-GBM, where survival probability improves substantially with time survived. The CS-based nomogram and online tool offers a novel, clinically actionable framework for personalized risk assessment and survivorship planning. Integration of dynamic modeling with molecularly informed approaches may further refine prognosis and guide therapeutic strategies in this devastating pediatric cancer.

Indexed as

incidencenomogrampediatric glioblastoma (p-GBM)Surveillance, Epidemiology, and End Results (SEER)survival

Identifiers

PMID42305501
PMCPMC13265230

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.