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Plasma Epstein–Barr Virus DNA and Risk of Future Nasopharyngeal Cancer

癌症 医学 鼻咽癌 内科学 置信区间 鼻咽癌 前瞻性队列研究 肿瘤科 胃肠病学 阶段(地层学) 癌症筛查 免疫学 生物 放射治疗 古生物学
作者
K. C. Allen Chan,Wah‐Kit Lam,Ann D. King,Vincent Lin,Patrick P.H. Lee,Benny Zee,Stephen L. Chan,I.O.L. Tse,Adley Tsang,M. Li,Peiyong Jiang,Qi Yong H. Ai,Darren M.C. Poon,Kwok‐Hung Au,Edwin P. Hui,Brigette B.Y.,Andrew C. van Hasselt,Anthony T.C. Chan,John K. S. Woo,Y.M. Dennis Lo
出处
期刊:NEJM evidence [New England Journal of Medicine]
卷期号:2 (7) 被引量:3
标识
DOI:10.1056/evidoa2200309
摘要

BackgroundWe previously conducted a prospective study to show that nasopharyngeal cancer (NPC) screening with circulating Epstein–Barr virus (EBV) DNA analysis can improve survival. However, the long-term significance of positive results in individuals without cancer was unclear.MethodsWe conducted a second-round screening at a median of 43 months after the initial screening. Participants with detectable plasma EBV DNA were retested in 4 weeks, and those with persistently positive results were investigated with nasal endoscopy and magnetic resonance imaging.ResultsOf the 20,174 volunteers who participated in the first-round screening, 17,838 (88.6%) were rescreened. Among them, 423 (2.37%) had persistently detectable plasma EBV DNA. Twenty-four patients were identified as having NPC. A significantly higher proportion of patients had stage I/II cancer than in a historical cohort (67% vs. 20%; chi-square test, P<0.001), and they had superior 3-year progression-free survival (100% vs. 78.8%). Compared with participants with undetectable plasma EBV DNA in the first round of screening, participants with transiently and persistently positive results in the first round were more likely to have a cancer identified in the second round, with relative risks of 4.4 (95% confidence interval, 1.3 to 15.0) and 16.8 (95% confidence interval, 5.7 to 49.6), respectively.ConclusionsIndividuals with detectable plasma EBV DNA but without an immediately identifiable NPC were more likely to have the cancer identified in another round of screening performed 3 to 5 years later. (Funded by Kadoorie Charitable Foundation and others; ClinicalTrials.gov number, NCT02063399.)
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