AI Article Synopsis

  • The rise of oropharyngeal cancer (OPC) linked to HPV in men emphasizes the urgent need for effective early screening tests, especially since recurrence and metastasis rates are high.
  • A previous study identified a significant correlation between the methylation of the EPB41L3 tumor suppressor gene and HPV16 in the oral gargle of OPC patients, with higher levels found in those with the cancer compared to healthy controls.
  • Expanding research to include 228 OPC cases reinforced the utility of HPV16/EPB41L3 methylation as a potential biomarker, achieving a sensitivity of 76% for early cases; however, the need for additional biomarkers remains to enhance early detection capabilities.

Article Abstract

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582688PMC
http://dx.doi.org/10.1002/cam4.4757DOI Listing

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