列线图
医学
内科学
阶段(地层学)
一致性
鼻咽癌
肿瘤科
临床终点
比例危险模型
生存分析
危险系数
外科
多元分析
放射治疗
回顾性队列研究
预测模型
单变量分析
队列
存活率
AJCC分段系统
T级
接收机工作特性
作者
Xue Song Sun,Yu Jing Liang,Guo Dong Jia,Sai Lan Liu,Li Ting Liu,Shan Shan Guo,Rui Sun,Dong Hua Luo,Qiu Yan Chen,Lin Quan Tang,Hai Qiang Mai
出处
期刊:Oral Oncology
[Elsevier]
日期:2020-04-13
卷期号:106: 104711-104711
被引量:5
标识
DOI:10.1016/j.oraloncology.2020.104711
摘要
• Three hundreds and three patients with lrNPC were retrospectively reviewed. • Four independent prognostic factors were included in nomogram. • The C-index of the nomogram was 0.687. • Local treatment benefited patients in the low- and intermediate-risk groups. • High-risk patients could not benefit from local treatment. Thus far, there is no final conclusion on the treatment of local recurrent nasopharyngeal carcinoma (lrNPC) patients. Herein, we developed a nomogram which combined prognostic biomarkers to predict clinical outcome and guide individual treatment. From 2006 to 2016, 303 patients with lrNPC were retrospectively reviewed. Overall survival (OS) was the primary endpoint. The nomogram was established with the significant prognostic factors (P < 0.05) selected by multivariate analysis using Cox regression model. Harrell Concordance Index (C-index), calibration curves, and decision curve analysis (DCA) were applied to evaluate this model. Four independent prognostic factors (age, hypertension, relapsed T (rT) stage, and Epstein-Barr virus DNA) identified from multivariable analysis were included into the nomogram. The C-index of the nomogram was 0.687. The calibration curves for 1-, 3-, and 5-year OS rate showed satisfactory agreements between the predicted and actual values. The decision curve analysis also exhibited a preferable net benefit of this model. All patients were subdivided into three risk groups based on the nomogram. Local treatment was associated with higher OS than palliative chemotherapy alone in the low (P < 0.001) and intermediate-risk groups (P = 0.001). However, no significant difference was observed between different treatment methods in the high-risk group (P = 0.176). We established the nomogram for patients with lrNPC to predict OS and guide individual treatment, which showed satisfactory performance in accuracy, discrimination capability, and clinical utility.
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