Development of a Nomogram and Risk Grouping System for Predicting 1-Year Overall Survival of Patients With Atypical Teratoid/Rhabdoid Tumors.

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Journal of Child Neurology Pub Date : 2025-03-01 Epub Date: 2025-01-27 DOI:10.1177/08830738241281393
Xu Kang, Yabing Zhou, Fangjie Shen, Jiaqi Feng, Yunkun Wang, Jie Ma, Qiang Qiang, Xiaoqiang Wang
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引用次数: 0

Abstract

PurposeAtypical teratoid/rhabdoid tumor (AT/RT) is a kind of central nervous system malignant tumor in children. In this study, we aimed to develop a practically clinical nomogram and risk grouping system to predict 1-year overall survival for patients with atypical teratoid/rhabdoid tumor.MethodsThe nomogram was constructed based on the pediatric tumor registry of Xinhua Hospital affiliated to Shanghai Jiaotong University School of Medicine. Fifty-four information-integrated patients with atypical teratoid/rhabdoid tumor were included from the database. Cox regression analyses were used to select independent prognostic factors. Based on the fitted multivariate Cox regression model, a nomogram of 1-year overall survival for atypical teratoid/rhabdoid tumor patients was generated. Moreover, the nomogram was validated by assessing its discrimination and calibration.ResultsIn these patients, age at diagnosis, the extent of tumor resection, radiotherapy, and chemotherapy were included in the multivariate Cox regression model. Based on this multivariate Cox regression model, a nomogram of 1-year overall survival for atypical teratoid/rhabdoid tumor patients was generated. The nomogram had good discrimination (the concordance index was 0.781) and calibration curves showed no deviation from reference lines. Decision curve analysis demonstrated this nomogram was useful for clinical practice. The risk grouping system was built based on nomogram-derived risk scores, which could classify patients into 3 risk groups. Compared with the low-risk group, the risk of 1-year death was significantly higher in the intermediate-risk group (hazard ratio = 1.42, 95%, confidence intervals = 0.49-4.11) and high-risk group (hazard ratio = 9.78, 95% confidence intervals = 3.53-27.1).ConclusionA nomogram and risk grouping system were built to predict for the 1-year overall survival of atypical teratoid/rhabdoid tumor patients. The nomogram could facilitate a personalized prognostic evaluation for atypical teratoid/rhabdoid tumor patients and help medical practitioners make better treatment.

开发用于预测非典型畸形/横纹肌瘤患者 1 年总生存期的提名图和风险分组系统
目的:不典型畸胎瘤/横纹肌样瘤(AT/RT)是一种儿童中枢神经系统恶性肿瘤。在这项研究中,我们旨在建立一个实用的临床nomogram和风险分组系统来预测非典型畸胎瘤/横纹肌样瘤患者的1年总生存率。方法:以上海交通大学医学院附属新华医院儿童肿瘤登记资料为基础构建nomogram。54例非典型畸胎瘤/横纹肌样瘤患者纳入数据库。采用Cox回归分析选择独立预后因素。根据拟合的多变量Cox回归模型,生成非典型畸胎瘤/横纹肌样肿瘤患者1年总生存率的nomogram。此外,通过判别和定标对模态图进行验证。结果:多因素Cox回归模型包括诊断年龄、肿瘤切除程度、放疗和化疗。基于该多变量Cox回归模型,生成非典型畸胎瘤/横纹肌样肿瘤患者1年总生存率的nomogram。模态图判别性好(一致性指数为0.781),标定曲线与参考线无偏差。决策曲线分析表明,该图对临床实践是有用的。基于nomogram衍生风险评分建立风险分组系统,将患者分为3个风险组。与低危组相比,中危组(风险比= 1.42,95%,可信区间= 0.49 ~ 4.11)和高危组(风险比= 9.78,95%可信区间= 3.53 ~ 27.1)的1年死亡风险显著高于低危组。结论:建立了非典型畸胎瘤/横纹肌样瘤患者1年总生存率的nomogram及风险分型系统。对非典型畸胎瘤/横纹肌样瘤患者进行个性化的预后评估,帮助医生更好地治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Child Neurology
Journal of Child Neurology 医学-临床神经学
CiteScore
4.20
自引率
5.30%
发文量
111
审稿时长
3-6 weeks
期刊介绍: The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.
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