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Clinical features and outcomes of pediatric intracranial gliomas: results from single center’s 226 cases and corroborated with SEER database

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Abstract

Background

Pediatric gliomas are the most common central nervous system (CNS) tumors in children and adolescents and show different clinical and histopathological characteristics from the adult. The prognostic factors were poorly defined in pediatric intracranial gliomas.

Methods

We collected pediatric intracranial glioma cases in our institution between February 2011 and June 2022. The patient clinical data, tumor growth characteristics, treatments, and follow-up data were analyzed by Cox regression analysis to identify impact factors on the prognosis of pediatric intracranial glioma patients. To corroborate our data, an independent cohort of pediatric intracranial glioma from the Surveillance, Epidemiology, and End Results Program (SEER) database was analyzed.

Results

A total of 181 cases of pediatric low-grade glioma (PLGG) and 45 cases of pediatric high-grade glioma (PHGG) were included. In multivariate Cox regression analysis, tumor size > 59.5 mm (p = 0.006) and non-gross total resection (non-GTR; subtotal resection, STR, p = 0.042; biopsy, p = 0.012) were associated with decreased overall survival (OS) in PLGG patients. In PHGG patients, only chemotherapy (p = 0.023) was associated with OS while tumor size was marginally prognostic for OS (p = 0.051). Additional independent analysis of 2734 PLGG and 741 PHGG from the SEER database corroborated that larger tumor size was associated with decreased OS in LGG (p = 0.001) and HGG (p < 0.001) patients, separately.

Conclusion

In this study, we found that tumor size was a significant prognostic factor for the OS of PLGG patients in our series. Besides the tumor size, the extent of resection also independently impacted the prognosis of PLGG patients. While in PHGG patients, only chemotherapy was associated with improved OS and tumor size was marginally prognostic.

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Data availability

The original contributions presented in the study are presented in the article or Supplementary Material. Upon reasonable request, the corresponding authors will provide further data.

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Funding

This work was supported by the National Natural Science Foundation of China (82072795, Feng Wan). No other specific grant was received for this research from the public, commercial, or not-for-profit funding agencies.

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Authors and Affiliations

Authors

Contributions

Conception and design: Feng Wan; acquisition of clinical information and data: Zirong Chen, Zhongyin Guo, Junhong Wang; analysis and interpretation of data: Zirong Chen, Junhong Wang; reviewing, and/or revising the manuscript: Zirong Chen, Dan Cao, Yu Xu, Fangyong Dong, and Feng Wan. The final manuscript was read and approved by all authors.

Corresponding author

Correspondence to Feng Wan.

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Ethics approval

An Institutional Review Board (IRB) from Tongji Hospital, Tongji Medical School, Huazhong University Science and Technology approved the collection of all clinical information used in this study (TJ-IRB20211271).

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Chen, Z., Guo, Z., Wang, J. et al. Clinical features and outcomes of pediatric intracranial gliomas: results from single center’s 226 cases and corroborated with SEER database. Childs Nerv Syst 39, 593–601 (2023). https://doi.org/10.1007/s00381-023-05841-3

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  • DOI: https://doi.org/10.1007/s00381-023-05841-3

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