Center for Immunization and Infection Research in Cancer, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Department of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA.
Cancer Med. 2022 Oct;11(20):3735-3742. doi: 10.1002/cam4.4757. Epub 2022 May 26.
As oropharyngeal cancer (OPC) associated with human papillomavirus (HPV) increases in men, the need for a screening test to diagnose OPC early is crucial. While HPV-associated OPC has a favorable prognosis, recurrence is likely, and metastatic OPC is often incurable regardless of HPV status. Our previous study of pretreatment, male OPC cases (n = 101) and age- and smoking-matched controls (n = 101) found methylation of the host EPB41L3 tumor suppressor gene and HPV16 in the oral gargle was correlated with these biomarkers in the tumor. Methylation of these genes in the oral gargle was significantly (p < 0.0001) higher among cases compared to controls. To further study the utility of HPV16/EPB41L3 methylation, we expanded the sample size and specifically increased the number of early OPC cases (T1-T2, N0-N1; small tumors with a single ipsilateral node <3 cm) to evaluate these biomarkers in early and late OPC. This study included 228 OPC cases, 92 of which were early cases and frequency matched to 142 healthy controls. In logistic regression, the AUC for HPV16/EPB41L3 methylation for all OPC cases was 0.82. Among early and late OPC cases, the AUC was 0.78 and 0.85, respectively. For early cases, 76% sensitivity was achieved, replicating results from our prior study, with a specificity of 65%, indicating room for improvement. The ability of HPV16/EPB41L3 methylation to distinguish OPC from healthy controls highlights its utility as a potential biomarker for OPC. However, the inability to predict early OPC better than late stage OPC indicates the need for additional biomarkers to improve screening performance.
随着与人类乳头瘤病毒(HPV)相关的口咽癌(OPC)在男性中发病率的上升,需要一种筛查测试来早期诊断 OPC,这一点至关重要。虽然 HPV 相关的 OPC 预后良好,但仍有可能复发,转移性 OPC 通常是不可治愈的,而不管 HPV 状态如何。我们之前对男性 OPC 病例(n=101)和年龄及吸烟匹配对照(n=101)进行的研究发现,口腔漱口液中宿主 EPB41L3 肿瘤抑制基因和 HPV16 的甲基化与肿瘤中的这些生物标志物相关。与对照组相比,病例组口腔漱口液中这些基因的甲基化水平显著更高(p<0.0001)。为了进一步研究 HPV16/EPB41L3 甲基化的效用,我们扩大了样本量,并特别增加了早期 OPC 病例(T1-T2,N0-N1;单侧单个淋巴结<3cm 的小肿瘤)的数量,以评估这些生物标志物在早期和晚期 OPC 中的作用。这项研究包括 228 例 OPC 病例,其中 92 例为早期病例,并与 142 例健康对照进行了频率匹配。在逻辑回归中,所有 OPC 病例 HPV16/EPB41L3 甲基化的 AUC 为 0.82。在早期和晚期 OPC 病例中,AUC 分别为 0.78 和 0.85。对于早期病例,76%的敏感性与我们之前的研究结果一致,特异性为 65%,表明仍有改进的空间。HPV16/EPB41L3 甲基化能够区分 OPC 与健康对照,突出了其作为 OPC 潜在生物标志物的效用。然而,它不能比晚期 OPC 更好地预测早期 OPC,这表明需要额外的生物标志物来提高筛查性能。