儿科颅内外胚乳瘤:来自全国癌症数据库的护理模式、差异和生存结果。

IF 2.1 3区 医学 Q3 CLINICAL NEUROLOGY
Pemla Jagtiani, Mert Karabacak, Chi Le, Zeynep Bahadir, Peter F Morgenstern, Konstantinos Margetis
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引用次数: 0

摘要

研究目的本研究旨在提取和分析美国国家癌症数据库(NCDB)中的综合数据,以深入了解与儿科患者颅内上皮瘤相关的流行病学发病率、治疗模式和生存结果:作者研究了从NCDB中提取的2010年至2017年的数据,重点研究了0-21岁个体的颅内附乳瘤。研究采用逻辑回归和泊松回归,以及卡普兰-梅耶生存估计和考克斯比例危险模型进行分析:在纳入的908名儿科患者中,495人(54.5%)为男性,702人(80.6%)为白人。卡普兰-梅耶尔分析确定,诊断后1年的总生存率(OS)为97.1%(95% CI 96%-98.2%),3年为89%(95% CI 86.9%-91.1%),5年为82.9%(95% CI 80.3%-85.7%),10年为74.5%(95% CI 69.8%-79.4%)。3级肿瘤预示的死亡风险高出4倍多(P < 0.001;参考值 = 2级)。脑室下定位也与死亡率增加1.7倍有关(p = 0.002;参考值 = 脑室上)。肿瘤最大尺寸越大(> 5 厘米),死亡率越低(HR 0.64,p = 0.011;参考值 ≤ 5 厘米)。绝大多数患者(85.9%,n = 780)接受了切除术。未参保患者延长住院时间(LOS)的几率是参保患者的四倍多(OR 4.645,P = 0.007)。76.1%的患者接受了放疗,5-12岁儿童接受放疗的比例最高(p < 0.001)。只有25.6%的患者在治疗过程中的任何阶段接受了化疗。化疗的高峰期出现在0-4岁年龄组,该年龄组的化疗率高达33.6%。Kaplan-Meier分析表明,化疗与较差的OS显著相关(p = 0.041):对 NCDB 的全面分析为了解儿童颅内外胚瘤瘤的流行病学、治疗模式和生存结果提供了宝贵的信息。较高的肿瘤分级、颅内下定位和化疗的使用与较差的OS相关,而较大的肿瘤体积与较低的死亡率相关。研究还发现了护理方面的差异,未参保患者的住院时间更长。这些发现强调了根据患者和肿瘤特征制定针对性治疗策略的必要性,并突出了消除社会经济障碍以优化儿童肾上腺瘤患者预后的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intracranial ependymomas in pediatric patients: patterns of care, disparities, and survival outcomes from the National Cancer Database.

Objective: This study aimed to extract and analyze comprehensive data from the National Cancer Database (NCDB) to gain insights into the epidemiological prevalence, treatment patterns, and survival outcomes associated with intracranial ependymomas in pediatric patients.

Methods: The authors examined data extracted from the NCDB spanning the years 2010 to 2017, with a specific emphasis on intracranial ependymomas in individuals aged 0-21 years. The study used logistic and Poisson regression, along with Kaplan-Meier survival estimates and Cox proportional hazards models, for analysis.

Results: Among 908 included pediatric patients, 495 (54.5%) were male, and 702 (80.6%) were White. Kaplan-Meier analysis determined overall survival (OS) rates of 97.1% (95% CI 96%-98.2%) at 1 year postdiagnosis, 89% (95% CI 86.9%-91.1%) at 3 years, 82.9% (95% CI 80.3%-85.7%) at 5 years, and 74.5% (95% CI 69.8%-79.4%) at 10 years. Grade 3 tumors predicted a more than fourfold higher mortality hazard (p < 0.001; reference = grade 2). Infratentorial localization was also associated with a 1.7-fold increase in mortality hazard (p = 0.002; reference = supratentorial). Larger maximum tumor size (> 5 cm) correlated with a lower mortality hazard (HR 0.64, p = 0.011; reference ≤ 5 cm). The vast majority of patients (85.9%, n = 780) underwent resection. Uninsured patients had over fourfold higher prolonged length of stay (LOS) odds than those privately insured (OR 4.645, p = 0.007). Radiotherapy was received by 76.1% of patients, and the highest rates of radiotherapy occurred among children aged 5-12 years (p < 0.001). Only 25.6% received chemotherapy at any point during their treatment. Peak chemotherapy use emerged within ages 0-4 years, reaching 33.6% in this age group. Kaplan-Meier analysis indicated chemotherapy was associated with significantly worse OS (p = 0.041).

Conclusions: This comprehensive analysis of the NCDB provides valuable insights into the epidemiology, treatment patterns, and survival outcomes of intracranial ependymomas in pediatric patients. Higher tumor grade, infratentorial localization, and chemotherapy use was associated with worse OS, while larger tumor size correlated with lower mortality hazard. Disparities in care were identified, with uninsured patients experiencing prolonged LOS. These findings underscore the need for tailored treatment strategies based on patient and tumor characteristics and highlight the importance of addressing socioeconomic barriers to optimize outcomes for children with ependymomas.

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来源期刊
Journal of neurosurgery. Pediatrics
Journal of neurosurgery. Pediatrics 医学-临床神经学
CiteScore
3.40
自引率
10.50%
发文量
307
审稿时长
2 months
期刊介绍: Information not localiced
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