俞霞, 季明芳, 程伟民, 黄玉玲, 李付贵. EBV 抗体和EBV-DNA 在鼻咽癌诊断及分期的研究*[J]. 中国肿瘤临床, 2016, 43(15): 650-654. DOI: 10.3969/j.issn.1000-8179.2016.15.393
引用本文: 俞霞, 季明芳, 程伟民, 黄玉玲, 李付贵. EBV 抗体和EBV-DNA 在鼻咽癌诊断及分期的研究*[J]. 中国肿瘤临床, 2016, 43(15): 650-654. DOI: 10.3969/j.issn.1000-8179.2016.15.393
Xia YU, Mingfang JI, Weimin CHENG, Yuling HUANG, Fugui LI. Assessment of EBV antibodies and EBV- DNA in the diagnosis and stages of nasopharyngeal carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2016, 43(15): 650-654. DOI: 10.3969/j.issn.1000-8179.2016.15.393
Citation: Xia YU, Mingfang JI, Weimin CHENG, Yuling HUANG, Fugui LI. Assessment of EBV antibodies and EBV- DNA in the diagnosis and stages of nasopharyngeal carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2016, 43(15): 650-654. DOI: 10.3969/j.issn.1000-8179.2016.15.393

EBV 抗体和EBV-DNA 在鼻咽癌诊断及分期的研究*

Assessment of EBV antibodies and EBV- DNA in the diagnosis and stages of nasopharyngeal carcinoma

  • 摘要: 目的:评估EBNA1/IgA 、Zta/IgA 、VCA/IgA 和EBV-DNA对不同分期鼻咽癌的诊断效能,探讨各指标阳性率与鼻咽癌分期的关系。方法:收集2010年3 月至2015年9 月中山大学附属中山医院收治的初诊鼻咽癌患者152 例,健康体检者675 例。采用酶联免疫吸附法(ELISA)检测血清EBNA1/IgA 、Zta/IgA 和VCA/IgA 抗体ROD 值,荧光定量PCR (fluorescence quantitative PCR,FQ-PCR )检测血浆EBV-DNA水平。比较单独和联合应用EBV 标记物对各期鼻咽癌的诊断效能,同时分析各指标阳性率与鼻咽癌分期的关系。结果:鼻咽癌患者EBNA1/IgA 、Zta/IgA 、VCA/IgA 和EBV-DNA阳性率显著高于健康体检者(P < 0.01)。 EBNA1/IgA 在早期鼻咽癌表达相对较高,灵敏度为77.8% ,而EBV-DNA在晚期鼻咽癌的灵敏度最高为88.8% ,两者特异度均在96% 以上。联合检测中EBNA1/IgA 并联EBV-DNA检测的灵敏度为92.1%(早期为82.5% 、晚期为98.9%),特异度为96.9% 。EBV-DNA阳性率与鼻咽癌临床分期和N 分期呈正相关,Zta/IgA 阳性率与N 分期呈正相关(P < 0.01)。 结论:在无症状人群中进行鼻咽癌筛查,单项指标首选EBNA1/IgA 。晚期患者的辅助诊断则推荐EBV-DNA。两者并联检测可进一步提高鼻咽癌诊断效能。EBV-DNA是鼻咽癌分期和病情监测的重要指标,Zta/IgA 可间接反映淋巴结转移情况,有望对患者病情评估起到参考作用。

     

    Abstract: To evaluate the efficacy of Epstein-Barr nuclear antigen 1/immunoglobulin A (EBNA 1/IgA), BamH 1 Z transactivator/IgA (Zta/IgA), capsid antigen/IgA (VCA/IgA), and Epstein-Barr virus deoxyribonucleic acid (EBV-DNA) in detecting different stages of na -sopharyngeal carcinoma (NPC). The relationship between the EBV markers and stages of NPC was also analyzed. Methods:Blood sam-ples of 152 untreated patients with NPC and 675 healthy subjects were collected.ELISA was used to detect the serum levels of EBNA 1/IgA, Zta/IgA, and VCA/IgA. Fluorescence quantitative PCR (FQ-PCR) was used to detect the plasma levels of EBV-DNA. ROC and correla -tion analyses were employed to assess the detection assays for NPC diagnosis. The positive rates of EBV markers in NPC patients in dif -ferent stages were analyzed statistically. Results: The positive rates of EBNA1/IgA, Zta/IgA, VCA/IgA, and EBV- DNA in NPC patients were higher than those in the healthy individuals. The expression of EBNA1/IgA was relatively high in early NPC. The sensitivity of EB -NA1/IgA was 77. 8% . In advanced NPC, the level of EBV- DNA was high, and the sensitivity of EBV- DNA was 88. 8% . The specificity of EBV-DNA and EBNA1/IgA could reach more than 96%. The combination of EBV-DNA and EBNA1/IgA showed the best diagnostic value, with a sensitivity of92. 1% (early stage 82. 5%, advanced stage 98. 9%) and a specificity of96. 9%. The positive rates of EBV-DNA were positively associated with the NPC clinic stage and N stage. The positives rates of Zta/IgA were positively associated with the NPC N stage. Conclusion: The best single index for NPC screening in an asymptomatic population is EBNA 1/IgA. EBV –DNA is an ideal index for auxiliary diagnostics of advanced NPC. The combination of EBV-DNA and EBNA 1/IgA shows the best diagnostic value. EBV-DNA is an important index in the stage and illness monitoring of NPC. Zta/IgA can indirectly reflect the character of lymph node metastasis, and it may be useful in assessment of NPC surveillance.

     

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