Hao Sheng-Po, Tsang Ngan-Ming, Chang Kai-Ping
Department of Otolaryngology, Chang Gung Memorial Hospital, Chang Gung University, Taipei, Taiwan, Republic of China.
Cancer. 2003 Apr 15;97(8):1909-13. doi: 10.1002/cncr.11312.
Nasopharyngeal carcinoma (NPC) is a common head and neck cancer in Taiwan. The goals of the current study were to investigate whether a nasopharyngeal swab technique could provide enough DNA for polymerase chain reaction (PCR) analysis of the Epstein-Barr virus (EBV)-derived latent membrane protein 1 (LMP-1) gene and to determine the feasibility and reliability of diagnosing NPC by detection of LMP-1 in the nasopharynx.
320 adults underwent nasopharyngoscopy and nasopharyngeal swab to obtain cells for the LMP-1 PCR assay; some patients also underwent nasopharyngeal biopsy.
An amount of DNA that was sufficient for PCR was extracted from 96.3% of the swab samples. By detecting LMP-1 in nasopharyngeal swabs, NPC was diagnosed with a false positive rate of 12.7% (7 of 55 patients), a false negative rate of 1.6% (4 of 253 patients), sensitivity of 87.3% (48 of 55 patients), specificity of 98.4% (249 of 253 patients), a positive predictive value of 92.3% (48 of 52 patients), and a negative predictive value of 97.3% (249/256 patients). NPC was diagnosed by nasopharyngoscopy with a false positive rate of 38% (30 of 79 patients), a false negative rate of 0.4% (1 of 241 patients), sensitivity of 62% (49 of 79 patients), specificity of 99.6% (240 of 241 patients), a positive predictive value of 98% (49 of 50 patients), and a negative predictive value of 88.9% (240 of 270 patients). Only 7 (0.2%) of 256 patients with a diagnosis other than NPC had LMP-1 detected in the nasopharyngeal space.
Detecting EBV genomic LMP-1 by nasopharyngeal swab diagnosed NPC with 87.3% sensitivity and 98.4% specificity. EBV genomic DNA usually is not detected by PCR-based methods in the nasopharyngeal space. Its incidence is estimated to be as low as 0.2% among the general population. The nasopharyngeal swab coupled with PCR-based EBV LMP-1 detection could serve as part of a screening program for high-risk populations.
鼻咽癌(NPC)是台湾常见的头颈部癌症。本研究的目的是调查鼻咽拭子技术是否能提供足够的DNA用于对爱泼斯坦-巴尔病毒(EBV)衍生的潜伏膜蛋白1(LMP-1)基因进行聚合酶链反应(PCR)分析,并通过检测鼻咽部的LMP-1来确定诊断NPC的可行性和可靠性。
320名成年人接受了鼻咽镜检查和鼻咽拭子检查,以获取用于LMP-1 PCR检测的细胞;部分患者还接受了鼻咽活检。
96.3%的拭子样本提取出了足以进行PCR的DNA量。通过检测鼻咽拭子中的LMP-1,诊断NPC的假阳性率为12.7%(55名患者中的7名),假阴性率为1.6%(253名患者中的4名),敏感性为87.3%(55名患者中的48名),特异性为98.4%(253名患者中的249名),阳性预测值为92.3%(52名患者中的48名),阴性预测值为97.3%(256名患者中的249名)。通过鼻咽镜检查诊断NPC的假阳性率为38%(79名患者中的30名),假阴性率为0.4%(241名患者中的1名),敏感性为62%(79名患者中的49名),特异性为99.6%(241名患者中的240名),阳性预测值为98%(50名患者中的49名),阴性预测值为88.9%(270名患者中的240名)。在256名非NPC诊断的患者中,只有7名(0.2%)在鼻咽部检测到LMP-1。
通过鼻咽拭子检测EBV基因组LMP-1诊断NPC的敏感性为87.3%,特异性为98.4%。基于PCR的方法通常在鼻咽部检测不到EBV基因组DNA。其在普通人群中的发生率估计低至0.2%。鼻咽拭子结合基于PCR的EBV LMP-1检测可作为高危人群筛查计划的一部分。