Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based Analysis

BackgroundWe aimed to analyze the epidemiology and outcomes of pediatric patients and adult patients with optic pathway gliomas in the United States using a population-based method.MethodsData for patients with optic pathway gliomas diagnosed between 2000 and 2018 were extracted from the SEER databa...

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Main Authors: Huanbing Liu, Yong Chen, Xiaowei Qin, Zheng Jin, Yining Jiang, Yubo Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-02-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.789856/full
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author Huanbing Liu
Yong Chen
Xiaowei Qin
Zheng Jin
Yining Jiang
Yubo Wang
author_facet Huanbing Liu
Yong Chen
Xiaowei Qin
Zheng Jin
Yining Jiang
Yubo Wang
author_sort Huanbing Liu
collection DOAJ
description BackgroundWe aimed to analyze the epidemiology and outcomes of pediatric patients and adult patients with optic pathway gliomas in the United States using a population-based method.MethodsData for patients with optic pathway gliomas diagnosed between 2000 and 2018 were extracted from the SEER database. We divided the patients into a pediatric group and an adult group. Descriptive analyses were conducted to analyze demographic and clinical characteristics and treatment. We used the chi-square test to evaluate differences between pediatric and adult patients with optic pathway gliomas. The possible prognostic indicators were analyzed by Kaplan–Meier curves and Cox proportional hazards models.ResultsOptic pathway gliomas represented 86.6% of all lesions originating from the optic pathway. In total, 1257 cases of optic pathway gliomas were included in our study. Pediatric patients accounted for 83.7% in this cohort, and most of the patients were diagnosed at 1-4 years old. Chemotherapy was chosen most often for pediatric patients, but radiation therapy was chosen most often for adult patients. Pilocytic astrocytoma accounted for 59.1% of pediatric patients and 37.5% of adult patients. The overall survival (OS) rates were 94.8% 5 years after diagnosis and 93.0% 10 years after diagnosis. Survival analysis showed that surgery, radiation and chemotherapy did not help patients obtain a better prognosis. Overall, pediatric patients had a better prognosis.ConclusionOptic pathway gliomas are relatively rare lesions with good prognosis. They mostly affect children, and pilocytic astrocytoma is the most common histological diagnosis. Highly individualized treatment is essential for such patients.
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spelling doaj.art-1dfd4925df9545849322012d27a7b9b92022-12-21T23:44:25ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-02-011210.3389/fonc.2022.789856789856Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based AnalysisHuanbing LiuYong ChenXiaowei QinZheng JinYining JiangYubo WangBackgroundWe aimed to analyze the epidemiology and outcomes of pediatric patients and adult patients with optic pathway gliomas in the United States using a population-based method.MethodsData for patients with optic pathway gliomas diagnosed between 2000 and 2018 were extracted from the SEER database. We divided the patients into a pediatric group and an adult group. Descriptive analyses were conducted to analyze demographic and clinical characteristics and treatment. We used the chi-square test to evaluate differences between pediatric and adult patients with optic pathway gliomas. The possible prognostic indicators were analyzed by Kaplan–Meier curves and Cox proportional hazards models.ResultsOptic pathway gliomas represented 86.6% of all lesions originating from the optic pathway. In total, 1257 cases of optic pathway gliomas were included in our study. Pediatric patients accounted for 83.7% in this cohort, and most of the patients were diagnosed at 1-4 years old. Chemotherapy was chosen most often for pediatric patients, but radiation therapy was chosen most often for adult patients. Pilocytic astrocytoma accounted for 59.1% of pediatric patients and 37.5% of adult patients. The overall survival (OS) rates were 94.8% 5 years after diagnosis and 93.0% 10 years after diagnosis. Survival analysis showed that surgery, radiation and chemotherapy did not help patients obtain a better prognosis. Overall, pediatric patients had a better prognosis.ConclusionOptic pathway gliomas are relatively rare lesions with good prognosis. They mostly affect children, and pilocytic astrocytoma is the most common histological diagnosis. Highly individualized treatment is essential for such patients.https://www.frontiersin.org/articles/10.3389/fonc.2022.789856/fullepidemiologysurvivalSEER programCNS diseaseoptic pathway glioma
spellingShingle Huanbing Liu
Yong Chen
Xiaowei Qin
Zheng Jin
Yining Jiang
Yubo Wang
Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based Analysis
Frontiers in Oncology
epidemiology
survival
SEER program
CNS disease
optic pathway glioma
title Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based Analysis
title_full Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based Analysis
title_fullStr Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based Analysis
title_full_unstemmed Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based Analysis
title_short Epidemiology and Survival of Patients With Optic Pathway Gliomas: A Population-Based Analysis
title_sort epidemiology and survival of patients with optic pathway gliomas a population based analysis
topic epidemiology
survival
SEER program
CNS disease
optic pathway glioma
url https://www.frontiersin.org/articles/10.3389/fonc.2022.789856/full
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