Prognostic value of serum Epstein-Barr virus antibodies in patients with nasopharyngeal carcinoma and undetectable pretreatment Epstein-Barr virus DNA

被引:26
|
作者
Yao, Ji-Jin [1 ,2 ]
Lin, Li [1 ]
Jin, Ya-Nan [3 ]
Wang, Si-Yang [2 ]
Zhang, Wang-Jian [4 ]
Zhang, Fan [2 ]
Zhou, Guan-Qun [1 ]
Cheng, Zhi-Bin [2 ]
Qi, Zhen-Yu [1 ]
Sun, Ying [1 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, Collaborat Innovat Ctr Canc Med, Dept Radiat Oncol,State Key Lab Oncol South China, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Radiat Oncol, Zhuhai, Peoples R China
[3] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Dept Nasopharyngeal Carcinoma,Canc Ctr, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Sch Publ Hlth, Guangdong Key Lab Med, Dept Med Stat & Epidemiol,Hlth Informat Res Ctr, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Early antigen; Epstein-Barr virus antibodies; nasopharyngeal carcinoma; prognostic value; viral capsid antigen; HUMAN-PAPILLOMAVIRUS; STAGING SYSTEM; 7TH EDITION; RADIOTHERAPY; METASTASIS; MARKERS; RISK; LOAD;
D O I
10.1111/cas.13296
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epstein-Barr virus (EBV) is closely associated with nasopharyngeal carcinoma (NPC). Serum IgA antibodies against early antigen (EA-IgA) and viral capsid antigen (VCA-IgA) are the most commonly used to screen for NPC in endemic areas. However, the prognostic value of serum EA-IgA and VCA-IgA in patients with NPC is less clear. We hypothesize that serum EA-IgA and VCA-IgA levels have prognostic impact for survival outcomes in NPC patients with undetectable pretreatment EBV (pEBV) DNA. In this series, 334 patients with non-metastatic NPC and undetectable pEBV DNA were included. Serum EA-IgA and VCA-IgA were determined by ELISA. After analysis, serum EA-IgA and VCA-IgA loads correlated positively with T, N, and overall stage (all P < 0.05). Serum EA-IgA was not associated with survival outcome in univariable analyses. But patients with serum VCA-IgA >1:120 had significantly inferior 5-year progression-free survival (80.4% vs 89.6%, P = 0.025), distant metastasis-free survival (88.4% vs 94.8%, P = 0.050), and locoregional relapse-free survival (88.4% vs 95.6%, P = 0.023; log-rank test). Multivariable analyses revealed that N stage was the only independent prognostic factor (all P < 0.05), but the VCA-IgA became insignificant. Further analyses revealed that serum VCA-IgA was not an independent prognostic factor in early N (N0-1) or advanced N (N2-3) stage NPC. In summary, although both EA-IgA and VCA-IgA correlate strongly with TNM stage, our analyses do not suggest that these antibodies are prognostic biomarkers in patients with NPC and undetectable pEBV DNA.
引用
收藏
页码:1640 / 1646
页数:7
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