Potential pitfalls in incorporating plasma Epstein-Barr virus DNA in the management of nasopharyngeal carcinoma

被引:6
|
作者
Wong, Edwin C. Y. [1 ]
Hung, Jessica L. C. [1 ]
Ng, Wai T. [1 ]
机构
[1] Pamela Youde Nethersole Eastern Hosp, Dept Clin Oncol, 3 Lok Man Rd, Hong Kong, Peoples R China
关键词
biomarker; nasopharyngeal carcinoma; pitfalls; plasma EBV DNA; prognostication; MODULATED RADIATION-THERAPY; QUANTITATIVE-ANALYSIS; EBV DNA; PROGNOSTICATION; GUIDELINES; REMISSION; CANCER; LEVEL; LOAD;
D O I
10.1002/hed.26018
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background This study identifies potential pitfalls in incorporating plasma Epstein-Barr virus (EBV) DNA into the management of nasopharyngeal carcinoma (NPC). Methods A total of 208 NPC patients without distant metastasis who received radical treatment and had measurements of EBV DNA at baseline, 8 weeks and 26 weeks postradiotherapy were analyzed. Prognostic and predictive values at each time-point were compared. Results Risk stratification by pretreatment level failed to identify a poor prognostic group. Detectable EBV DNA at 8 weeks and 26 weeks postradiotherapy were both associated with significantly poorer 5-year disease-free survival (HR 0.30, P < .001 and HR 0.03, P < .001, respectively) and overall survival (HR 0.27, P = .009 and HR 0.03, P < .001, respectively). Eighty percentage had detectable EBV DNA at recurrence (53.3% for local only, 100% for regional only, and 100% for distant failure). Conclusions Posttreatment EBV DNA, particularly at 26 weeks post-radiotherapy, has high prognostic and predictive values. Surveillance endoscopy/imaging are recommended for the detection of local recurrence.
引用
收藏
页码:446 / 455
页数:10
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