Eight-Signature Classifier for Prediction of Nasopharyngeal Carcinoma Survival

Author:

Wang Hai-Yun1,Sun Bing-Yu1,Zhu Zhi-Hua1,Chang Ellen T.1,To Ka-Fai1,Hwang Jacqueline S.G.1,Jiang Hao1,Kam Michael Koon-Ming1,Chen Gang1,Cheah Shie-Lee1,Lee Ming1,Liu Zhi-Wei1,Chen Jing1,Zhang Jia-Xing1,Zhang Hui-Zhong1,He Jie-Hua1,Chen Fa-Long1,Zhu Xiao-Dong1,Huang Ma-Yan1,Liao Ding-Zhun1,Fu Jia1,Shao Qiong1,Cai Man-Bo1,Du Zi-Ming1,Yan Li-Xu1,Hu Chun-Fang1,Ng Ho-Keung1,Wee Joseph T.S.1,Qian Chao-Nan1,Liu Qing1,Ernberg Ingemar1,Ye Weimin1,Adami Hans-Olov1,Chan Anthony T.1,Zeng Yi-Xin1,Shao Jian-Yong1

Affiliation:

1. Hai-Yun Wang, Zhi-Hua Zhu, Jing Chen, Jia-Xing Zhang, Hui-Zhong Zhang, Jie-Hua He, Ma-Yan Huang, Ding-Zhun Liao, Jia Fu, Qiong Shao, Man-Bo Cai, Zi-Ming Du, Li-Xu Yan, Chao-Nan Qian, Qing Liu, Yi-Xin Zeng, and Jian-Yong Shao, Sun Yat-sen University Cancer Center, Guangzhou; Bing-Yu Sun, Chinese Academy of Sciences, Hefei; Ka-Fai To, Michael Koon-Ming Kam, Ho-Keung Ng, and Anthony T. Chan, Chinese University of Hong Kong, Hong Kong; Fa-Long Chen and Xiao-Dong Zhu, Guangxi Medical University, Nanning; Hao...

Abstract

Purpose Currently, nasopharyngeal carcinoma (NPC) prognosis evaluation is based primarily on the TNM staging system. This study aims to identify prognostic markers for NPC. Patients and Methods We detected expression of 18 biomarkers by immunohistochemistry in NPC tumors from 209 patients and evaluated the association between gene expression level and disease-specific survival (DSS). We used support vector machine (SVM) –based methods to develop a prognostic classifier for NPC (NPC-SVM classifier). Further validation of the NPC-SVM classifier was performed in an independent cohort of 1,059 patients. Results The NPC-SVM classifier integrated patient sex and the protein expression level of seven genes, including Epstein-Barr virus latency membrane protein 1, CD147, caveolin-1, phospho-P70S6 kinase, matrix metalloproteinase 11, survivin, and secreted protein acidic and rich in cysteine. The NPC-SVM classifier distinguished patients with NPC into low- and high-risk groups with significant differences in 5-year DSS in the evaluated patients (87% v 37.7%; P < .001) in the validation cohort. In multivariate analysis adjusted for age, TNM stage, and histologic subtype, the NPC-SVM classifier was an independent predictor of 5-year DSS in the evaluated patients (hazard ratio, 4.9; 95% CI, 3.0 to 7.9) in the validation cohort. Conclusion As a powerful predictor of 5-year DSS among patients with NPC, the newly developed NPC-SVM classifier based on tumor-associated biomarkers will facilitate patient counseling and individualize management of patients with NPC.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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