Differences in Survival Among Infantile, Pediatric and Adult Intracranial Medulloblastoma: A SEER Analysis

IF 6.5 1区 医学 Q1 ONCOLOGY International Journal of Radiation Oncology Biology Physics Pub Date : 2025-03-01 Epub Date: 2025-02-03 DOI:10.1016/j.ijrobp.2024.11.027
V. Chua , M. Dumago , J. Jacinto , C. Villar , D. Tsang , J. Co
{"title":"Differences in Survival Among Infantile, Pediatric and Adult Intracranial Medulloblastoma: A SEER Analysis","authors":"V. Chua ,&nbsp;M. Dumago ,&nbsp;J. Jacinto ,&nbsp;C. Villar ,&nbsp;D. Tsang ,&nbsp;J. Co","doi":"10.1016/j.ijrobp.2024.11.027","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>Survival differences in infantile, paediatric, and adult medulloblastoma are unclear. This study aims to determine the difference in the overall survival among infant, pediatric and adult intracranial medulloblastomas and its associated factors</div></div><div><h3>Methods</h3><div>The National Cancer Institute-Surveillance, Epidemiology and End Results (SEER) database was queried for medulloblastoma from 2000 to 2020 using International Classification of Disease(ICD) for Oncology, with morphology codes 9470-9477/3. Age groups were divided into infantile (&lt;3years old), paediatric (3-18years old) and adult (&gt;18 years old). Rates of dying among infantile and adult medulloblastoma were compared to the rate among pediatric medulloblastomas. Chi-squared test was used for categorical variable. Cox-proportional analysis was used, Kaplan-Meier survival curves were generated for the three cohorts and log rank test was performed.</div></div><div><h3>Results</h3><div>1,991 patients were included: infantile(372,18.68%), paediatric(1,026,51.53%) and adult(593,29.78%) medulloblastoma. The 3-year overall survival (OS) were 69.81%, 84.62%, 83.45%; the 5-year OS were 66.65%, 79.46%,76.45%; and the 10-year OS were 63.67%, 72.38% and 66.89% respectively for infantile, pediatric and adult medulloblastoma. Regional and distant disease, large cell medulloblastoma, less than complete surgery, non-receipt of radiotherapy and chemotherapy were associated with higher rate of dying. 297 patients were treated with chemotherapy but not radiotherapy, with majority (220, 74.07%) being infantile medulloblastoma. 216 (36%) of the adult medulloblastoma did not receive any chemotherapy. Less than 5% had molecular classification reported.</div><div>Crude hazard ratio(HR) of infantile compared to paediatric medulloblastoma is 1.65 (95%CI:1.33-2.04). After adjusting for gender, histology/molecular subtyping and receipt of radiotherapy, the HR decreased to 1.29(95%CI:1.01-1.66). Crude HR of adult compared to pediatric medulloblastoma is 1.24(95%CI:1.02-1.51). After adjusting for gender, histology/molecular subtyping and receipt of chemotherapy, the HR decreased to 1.10(95%CI:0.89-1.37).</div></div><div><h3>Conclusion</h3><div>There is a survival difference among infantile, paediatric and adult medulloblastoma. The difference appeared to decrease when adjusted for the treatment and biology.</div></div>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":"121 3","pages":"Pages e6-e7"},"PeriodicalIF":6.5000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Radiation Oncology Biology Physics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0360301624036010","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/3 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective

Survival differences in infantile, paediatric, and adult medulloblastoma are unclear. This study aims to determine the difference in the overall survival among infant, pediatric and adult intracranial medulloblastomas and its associated factors

Methods

The National Cancer Institute-Surveillance, Epidemiology and End Results (SEER) database was queried for medulloblastoma from 2000 to 2020 using International Classification of Disease(ICD) for Oncology, with morphology codes 9470-9477/3. Age groups were divided into infantile (<3years old), paediatric (3-18years old) and adult (>18 years old). Rates of dying among infantile and adult medulloblastoma were compared to the rate among pediatric medulloblastomas. Chi-squared test was used for categorical variable. Cox-proportional analysis was used, Kaplan-Meier survival curves were generated for the three cohorts and log rank test was performed.

Results

1,991 patients were included: infantile(372,18.68%), paediatric(1,026,51.53%) and adult(593,29.78%) medulloblastoma. The 3-year overall survival (OS) were 69.81%, 84.62%, 83.45%; the 5-year OS were 66.65%, 79.46%,76.45%; and the 10-year OS were 63.67%, 72.38% and 66.89% respectively for infantile, pediatric and adult medulloblastoma. Regional and distant disease, large cell medulloblastoma, less than complete surgery, non-receipt of radiotherapy and chemotherapy were associated with higher rate of dying. 297 patients were treated with chemotherapy but not radiotherapy, with majority (220, 74.07%) being infantile medulloblastoma. 216 (36%) of the adult medulloblastoma did not receive any chemotherapy. Less than 5% had molecular classification reported.
Crude hazard ratio(HR) of infantile compared to paediatric medulloblastoma is 1.65 (95%CI:1.33-2.04). After adjusting for gender, histology/molecular subtyping and receipt of radiotherapy, the HR decreased to 1.29(95%CI:1.01-1.66). Crude HR of adult compared to pediatric medulloblastoma is 1.24(95%CI:1.02-1.51). After adjusting for gender, histology/molecular subtyping and receipt of chemotherapy, the HR decreased to 1.10(95%CI:0.89-1.37).

Conclusion

There is a survival difference among infantile, paediatric and adult medulloblastoma. The difference appeared to decrease when adjusted for the treatment and biology.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
婴儿、儿童和成人颅内髓母细胞瘤的生存差异:一项SEER分析
目的:目前尚不清楚婴儿、儿童和成人髓母细胞瘤的生存率差异。本研究旨在确定婴儿、儿童和成人颅内成神经管细胞瘤的总生存率差异及其相关因素。方法使用国际肿瘤疾病分类(ICD)查询美国国家癌症研究所(SEER)数据库2000 - 2020年的成神经管细胞瘤,形态学代码为9470-9477/3。年龄组分为婴儿(3岁)、儿科(3-18岁)和成人(18岁)。将婴儿和成人髓母细胞瘤的死亡率与儿童髓母细胞瘤的死亡率进行比较。分类变量采用卡方检验。采用cox -比例分析,生成三个队列的Kaplan-Meier生存曲线,并进行对数秩检验。结果共纳入1991例患者:婴儿(372例,18.68%)、儿童(1026例,51.53%)和成人(593例,29.78%)髓母细胞瘤。3年总生存率(OS)分别为69.81%、84.62%、83.45%;5年OS分别为66.65%、79.46%、76.45%;婴儿、儿童和成人髓母细胞瘤的10年OS分别为63.67%、72.38%和66.89%。局部和远处病变、大细胞髓母细胞瘤、手术不完全、未接受放疗和化疗与较高的死亡率相关。297例患者接受了化疗而非放疗,其中大多数(220例,74.07%)为婴儿髓母细胞瘤。216例(36%)成人成神经管细胞瘤未接受任何化疗。不到5%的人有分子分类报告。婴儿与儿童髓母细胞瘤的粗危险比(HR)为1.65 (95%CI:1.33-2.04)。在调整性别、组织学/分子分型和接受放射治疗后,HR降至1.29(95%CI:1.01-1.66)。成人与儿童髓母细胞瘤的粗HR为1.24(95%CI:1.02-1.51)。在调整性别、组织学/分子分型和接受化疗后,风险比降至1.10(95%CI:0.89-1.37)。结论小儿髓母细胞瘤与成人髓母细胞瘤存在生存差异。在调整了治疗和生物学因素后,这种差异似乎减小了。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
期刊最新文献
Alternative End-Joining Dependency Imposed by miR-21-5p Defines Radiation Resistance and a Targetable Vulnerability in Oral Squamous Cell Carcinoma. Erratum to 'Evaluation of Radiation Therapy Treatment Plans in a Randomized Phase 2 Trial Comparing 2 Schedules of Twice-Daily Thoracic Radiation Therapy in Limited Stage Small Cell Lung Cancer.' International Journal of Radiation Oncology*Biology*Physics, Volume 120, Issue 2, 1 October 2024, Pages 332-342. Stereotactic Reirradiation: Final Results From a Phase 1 Dose Escalation Trial (DESTROY-1) Perilesional Edema as a Predictor of Local Failure in Metastatic Brain Lesions Treated With Stereotactic Radiosurgery: A Systematic Review and Meta-Analysis Long-term Results From a Phase 1 Study of Spinal Cord Constraint Relaxation With Single Session Spine Stereotactic Radiosurgery in the Primary Management of Patients With Inoperable, Previously Unirradiated Spinal Metastases With Epidural Extension
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1