Correlation and prognosis analysis of human papillomavirus infection and P16 expression in oral and oropharyngeal squamous cell carcinomas

  • 0Department of Pathology, The Seventh Medical Center of PLA General Hospital, Beijinɡ, 100070, China.

|

|

Summary

This summary is machine-generated.

Human papillomavirus (HPV) DNA and P16 protein expression are more common in oropharyngeal squamous cell carcinoma (OPSCC) than oral squamous cell carcinoma (OSCC). P16 is a useful biomarker for HPV-related OPSCC but not OSCC, with age and stage impacting OSCC prognosis.

Area Of Science

  • Oncology
  • Virology
  • Pathology

Background

  • The incidence of human papillomavirus (HPV)-related oral squamous cell carcinomas (OSCC) and oropharyngeal squamous cell carcinomas (OPSCC) is rising.
  • The specific roles of HPV and P16 protein in the development and prognosis of OSCC and OPSCC remain incompletely understood and debated.

Purpose Of The Study

  • To investigate the prevalence and prognostic significance of HPV-DNA, HPV E6E7, and P16 protein expression in OSCC and OPSCC.
  • To explore the correlation between P16 protein expression and HPV infection in these cancer types.
  • To determine the clinical utility of P16 as a biomarker for HPV-related OSCC and OPSCC.

Main Methods

  • Analysis of HPV-DNA, HPV E6E7, and P16 protein expression in patient cohorts of OSCC and OPSCC.
  • Statistical evaluation of the prevalence of these markers in relation to tumor type, differentiation, and clinical parameters.
  • Correlation analysis between P16 expression and HPV infection status.
  • Prognostic analysis assessing the impact of HPV DNA and P16 expression on disease-free survival (DFS) and overall survival (OS).

Main Results

  • HPV DNA infection rate was significantly higher in OPSCC (16.7%) compared to OSCC (3.6%).
  • HPV DNA positivity correlated with poorly differentiated tumors (P=0.009).
  • P16 (+++) expression was significantly more frequent in OPSCC (12.5%) than OSCC (0.7%).
  • P16 (+++) demonstrated a sensitivity of 62.5% for detecting HPV DNA in OPSCC.
  • Neither HPV DNA nor P16 (+++) expression was significantly linked to prognosis in either OSCC or OPSCC.
  • In OSCC, age, T, N, and clinical stage correlated with prognosis. In OPSCC, younger age was associated with a better prognosis.

Conclusions

  • P16 (+++) serves as a reliable biomarker for HPV-related high-risk tumors in OPSCC but not in OSCC.
  • Prognostic factors in OSCC include patient age, tumor size (T), lymph node involvement (N), and clinical stage.
  • Younger age is a favorable prognostic indicator for patients with OPSCC.