Lin-Quan Tang1,2,*, Chao-Feng Li1,*, Jing Li1,*, Wen-Hui Chen1,*, Qiu-Yan Chen1,2, Lian-Xiong Yuan3, Xiao-Ping Lai4, Yun He4, Yun-Xiu-Xiu Xu4, Dong-Peng Hu4, Shi-Hua Wen4, Yu-Tuan Peng4, Lu Zhang1,2, Shan-Shan Guo1,2, Li-Ting Liu1,2, Ling Guo1,2,Yi-Shan Wu1,2, Dong-Hua Luo1,2, Pei-Yu Huang1,2, Hao-Yuan Mo1,2, Yan-Qun Xiang1,2, Rui Sun1,2, Ming-Yuan Chen1,2, Yi-Jun Hua1,2, Xing Lv1,2, Lin Wang1,2, Chong Zhao1,2, Ka-Jia Cao1,2,Chao-Nan Qian1,2, Xiang Guo1,2, Yi-Xin Zeng1,†, Hai-Qiang Mai1,2,† and Mu-Sheng Zeng1,†
Author Affiliations
1Sun Yat-sen University Cancer Center; State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine;
2Department of Nasopharyngeal Carcinoma;
3Department of Information Technology (CFL), Department of Medical Statistics and Epidemiology, the School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China;
4ZhongShan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.
*Authors contributed equally to this work.
†Authors contributed equally to this work.
Corresponding author:
Mu-Sheng Zeng, MD, PhD, Department of Experimental Research, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, 651 Dongfeng Road East, Guangzhou 510060, P. R. China (Email:zengmsh@mail.sysu.edu.cn).
Abstract
Background: This study aimed to establish an effective prognostic nomogram with or without plasma Epstein-Barr virus DNA (EBV DNA) for nondisseminated nasopharyngeal carcinoma (NPC).
Methods: The nomogram was based on a retrospective study of 4630 patients who underwent radiotherapy with or without chemotherapy at Sun Yat-sen University Cancer Center from 2007 to 2009. The predictive accuracy and discriminative ability of the nomogram were determined by a concordance index (C-index) and calibration curve and were compared with EBV DNA and the current staging system. The results were validated using bootstrap resampling and a prospective cohort study on 1819 patients consecutively enrolled from 2011 to 2012 at the same institution. All statistical tests were two-sided.
Results: Independent factors derived from multivariable analysis of the primary cohort to predict recurrence were age, sex, body mass index (BMI), T stage, N stage, plasma EBV DNA, pretreatment high sensitivity C-reactive protein (hs-CRP), lactate dehydrogenase (LDH), and hemoglobin level (HGB), which were all assembled into the nomogram with (nomogram B) or without EBV DNA (nomogram A). The calibration curve for the probability of recurrence showed that the nomogram-based predictions were in good agreement with actual observations. The C-index of nomogram B for predicting recurrence was 0.728 (P < .001), which was statistically higher than the C-index values for nomogram A (0.690), EBV DNA (0.680), and the current staging system (0.609). The C-index of nomogram B (0.730) and nomogram A (0.681) remained higher for predicting recurrence among patients treated with intensity-modulated radiotherapy (P < .001). The results were confirmed in the validation cohort.
Conclusions: The proposed nomogram with or without plasma EBV DNA resulted in more accurate prognostic prediction for NPC patients.
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