Tang Kai Dun, Baeten Kurt, Kenny Liz, Frazer Ian H, Scheper Gert, Punyadeera Chamindie
The School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology and the Translational Research Institute, Queensland 4059, Australia.
Janssen Diagnostics, Janssen Pharmaceutica NV, Beerse 2340, Belgium.
Cancers (Basel). 2019 Apr 3;11(4):473. doi: 10.3390/cancers11040473.
The incidence of human papillomavirus (HPV)-positive oropharyngeal cancer (OPC) is rising in high-income countries, including Australia. Increasing evidence suggests that accurate HPV testing is pivotal for clinical decision making and treatment planning in these patients. Recently, the eighth edition of the American Joint Committee on Cancer/Union for International Cancer Control (AJCC/UICC) tumor-node-metastasis (TNM) staging system for OPC (based on the p16INK4a (p16) status) was proposed and has been implemented. However, the applicability of this new staging system is still far from clear. In our study, = 127 OPC patients from Queensland, Australia were recruited, and the tumor p16 expression in these patients was examined using immunohistochemical (IHC) analysis. HPV-16 genotyping, viral load, and physical status (episomal versus integrated) in the saliva samples of OPC patients were determined using the qPCR method. A good inter-rater agreement ( = 0.612) was found between tumor p16 expression and oral HPV-16 infection in OPC. Importantly, according to the eighth edition staging system, HPV-16 DNA viral load (>10 copies/50 ng) was significantly associated with the advanced stages of OPC. In concordance with previous studies, a mixed HPV-16 form (partially or fully integrated) was predominately found in OPC patients. Taken together, our data support HPV-16 detection in saliva as a screening biomarker to identify people within the community who are at risk of developing OPC.
在包括澳大利亚在内的高收入国家,人乳头瘤病毒(HPV)阳性口咽癌(OPC)的发病率正在上升。越来越多的证据表明,准确的HPV检测对于这些患者的临床决策和治疗规划至关重要。最近,美国癌症联合委员会/国际癌症控制联盟(AJCC/UICC)提出并实施了OPC的第八版肿瘤-淋巴结-转移(TNM)分期系统(基于p16INK4a(p16)状态)。然而,这个新分期系统的适用性仍远不明确。在我们的研究中,招募了来自澳大利亚昆士兰州的127例OPC患者,并使用免疫组织化学(IHC)分析检测了这些患者肿瘤中的p16表达。采用qPCR方法测定了OPC患者唾液样本中的HPV-16基因分型、病毒载量和物理状态(游离型与整合型)。在OPC中,肿瘤p16表达与口腔HPV-16感染之间发现了良好的评分者间一致性(κ = 0.612)。重要的是,根据第八版分期系统,HPV-16 DNA病毒载量(>10拷贝/50 ng)与OPC的晚期显著相关。与先前的研究一致,在OPC患者中主要发现了混合的HPV-16形式(部分或完全整合)。综上所述,我们的数据支持将唾液中的HPV-16检测作为一种筛查生物标志物,以识别社区中具有OPC发病风险的人群。