Kreimer Aimée R, Johansson Mattias, Yanik Elizabeth L, Katki Hormuzd A, Check David P, Lang Kuhs Krystle A, Willhauck-Fleckenstein Martina, Holzinger Dana, Hildesheim Allan, Pfeiffer Ruth, Williams Craig, Freedman Neal D, Huang Wen-Yi, Purdue Mark P, Michel Angelika, Pawlita Michael, Brennan Paul, Waterboer Tim
Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
International Agency for Research on Cancer (IARC), Lyon, France
J Natl Cancer Inst. 2017 Aug 1;109(8). doi: 10.1093/jnci/djx005.
In a European cohort, it was previously reported that 35% of oropharyngeal cancer (OPC) patients were human papillomavirus type-16 (HPV16) seropositive up to 10 years before diagnosis vs 0.6% of cancer-free controls. Here, we describe the kinetics of HPV16-E6 antibodies prior to OPC diagnosis.
We used annual serial prediagnostic blood samples from the PLCO Cancer Screening Trial. Antibodies to HPV were initially assessed in prediagnostic blood drawn at study enrollment from 198 incident head and neck cancer patients (median years to cancer diagnosis = 6.6) and 924 matched control subjects using multiplex serology, and subsequently in serial samples (median = 5/individual). Available tumor samples were identified and tested for HPV16 RNA to define HPV-driven OPC.
HPV16-E6 antibodies were present at baseline in 42.3% of 52 OPC patients and 0.5% of 924 control subjects. HPV16-E6 antibody levels were highly elevated and stable across serial blood samples for 21 OPC patients who were seropositive at baseline, as well as for one OPC patient who seroconverted closer to diagnosis. All five subjects with HPV16-driven OPC tumors were HPV16-E6-seropositive, and the four subjects with HPV16-negative OPC tumors were seronegative. The estimated 10-year cumulative risk of OPC was 6.2% (95% confidence interval [CI] = 1.8% to 21.5%) for HPV16-E6-seropositive men, 1.3% (95% CI = 0.1% to 15.3%) for HPV16-E6-seropositive women, and 0.04% (95% CI = 0.03% to 0.06%) among HPV16-E6-seronegative individuals.
Forty-two percent of subjects diagnosed with OPC between 1994 and 2009 in a US cohort were HPV16-E6 seropositive, with stable antibody levels during annual follow-up for up to 13 years prior to diagnosis. Tumor analysis indicated that the sensitivity and specificity of HPV16-E6 antibodies were exceptionally high in predicting HPV-driven OPC.
在一项欧洲队列研究中,先前报告称,35%的口咽癌(OPC)患者在诊断前长达10年时人乳头瘤病毒16型(HPV16)血清学呈阳性,而无癌对照者的这一比例为0.6%。在此,我们描述了OPC诊断前HPV16-E6抗体的动力学变化。
我们使用了PLCO癌症筛查试验中每年的系列诊断前血液样本。最初,使用多重血清学方法对198例头颈癌患者(癌症诊断的中位时间 = 6.6年)和924名匹配对照者在研究入组时采集的诊断前血液中的HPV抗体进行评估,随后对系列样本(中位样本数 = 每人5份)进行评估。确定可用的肿瘤样本并检测HPV16 RNA,以定义HPV驱动的OPC。
在52例OPC患者中,42.3%在基线时存在HPV16-E6抗体,在924名对照者中这一比例为0.5%。对于21例基线时血清学呈阳性的OPC患者以及1例在更接近诊断时血清学转换的OPC患者,HPV16-E6抗体水平在系列血液样本中显著升高且保持稳定。所有5例HPV16驱动的OPC肿瘤患者HPV16-E6血清学呈阳性,4例HPV16阴性OPC肿瘤患者血清学呈阴性。HPV16-E6血清学呈阳性的男性OPC估计10年累积风险为6.2%(95%置信区间[CI] = 1.8%至21.5%),HPV16-E6血清学呈阳性的女性为1.3%(95% CI = 0.1%至15.3%),HPV16-E6血清学呈阴性个体中为0.04%(95% CI = 0.03%至0.06%)。
在美国队列中,1994年至2009年间诊断为OPC的患者中,42%的患者HPV16-E6血清学呈阳性,在诊断前长达13年的年度随访期间抗体水平保持稳定。肿瘤分析表明,HPV16-E6抗体在预测HPV驱动的OPC方面敏感性和特异性极高。