Yao Ji-Jin, Lin Li, Jin Ya-Nan, Wang Si-Yang, Zhang Wang-Jian, Zhang Fan, Zhou Guan-Qun, Cheng Zhi-Bin, Qi Zhen-Yu, Sun Ying
Department of Radiation Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Department of Radiation Oncology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China.
Cancer Sci. 2017 Aug;108(8):1640-1647. doi: 10.1111/cas.13296. Epub 2017 Jul 13.
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.
爱泼斯坦-巴尔病毒(EBV)与鼻咽癌(NPC)密切相关。在流行地区,血清抗早期抗原IgA抗体(EA-IgA)和病毒衣壳抗原IgA抗体(VCA-IgA)是筛查鼻咽癌最常用的指标。然而,血清EA-IgA和VCA-IgA在鼻咽癌患者中的预后价值尚不清楚。我们假设血清EA-IgA和VCA-IgA水平对预处理时EBV(pEBV)DNA检测不到的鼻咽癌患者的生存结局有预后影响。在本研究系列中,纳入了334例无转移且pEBV DNA检测不到的鼻咽癌患者。通过酶联免疫吸附测定法(ELISA)测定血清EA-IgA和VCA-IgA。分析后发现,血清EA-IgA和VCA-IgA载量与T分期、N分期和总分期呈正相关(均P<0.05)。在单因素分析中,血清EA-IgA与生存结局无关。但血清VCA-IgA>1:120的患者5年无进展生存率(80.4%对89.6%,P=0.025)、无远处转移生存率(88.4%对94.8%,P=0.050)和无局部区域复发生存率(88.4%对95.6%,P=0.023;对数秩检验)显著较差。多因素分析显示,N分期是唯一的独立预后因素(均P<0.05),但VCA-IgA变得无统计学意义。进一步分析表明,血清VCA-IgA在早期N(N0-1)或晚期N(N2-3)期鼻咽癌中不是独立的预后因素。总之,虽然EA-IgA和VCA-IgA均与TNM分期密切相关,但我们的分析并不表明这些抗体是pEBV DNA检测不到的鼻咽癌患者的预后生物标志物。