Abstract

HPV-DNA positive (HPVDNA+) oropharyngeal squamous cell carcinoma (OSCC) has better clinical outcome than HPV-DNA negative (HPVDNA-) OSCC. Current treatment may be unnecessarily extensive for most HPV+ OSCC, but before de-escalation, additional markers are needed together with HPV status to better predict treatment response. Here the influence of HLA class I/HLA class II expression was explored. Pre-treatment biopsies, from 439/484 OSCC patients diagnosed 2000-2009 and treated curatively, were analyzed for HLA I and II expression, p16INK4a and HPV DNA. Absent/weak as compared to high HLA class I intensity correlated to a very favorable disease-free survival (DFS), disease-specific survival (DSS) and overall survival (OS) in HPVDNA+ OSCC, both in univariate and multivariate analysis, while HLA class II had no impact. Notably, HPVDNA+ OSCC with absent/weak HLA class I responded equally well when treated with induction-chemo-radiotherapy (CRT) or radiotherapy (RT) alone. In patients with HPVDNA- OSCC, high HLA class I/class II expression correlated in general to a better clinical outcome. p16INK4a overexpression correlated to a better clinical outcome in HPVDNA+ OSCC. Absence of HLA class I intensity in HPVDNA+ OSCC suggests a very high survival independent of treatment and could possibly be used clinically to select patients for randomized trials de-escalating therapy.

Highlights

  • The incidence of oropharyngeal squamous cell carcinoma (OSCC) is increasing, mainly due to a rise in human papillomavirus (HPV) DNA positive HPV (HPVDNA+) OSCC, suggesting an epidemic of viral-induced OSCC[1,2,3,4]

  • In a previous smaller study, we showed that absent/weak HLA class I expression correlated with a very favorable outcome in HPVDNA+ tonsillar squamous cell carcinoma (TSCC), while the opposite was observed in HPVDNA- TSCC[13]

  • In this large cohort of OSCC patients, a significant correlation between absent/weak HLA class I expression and a very favorable clinical outcome was observed in HPVDNA+ OSCC, independent of treatment regime

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Summary

Introduction

The incidence of oropharyngeal squamous cell carcinoma (OSCC) is increasing, mainly due to a rise in human papillomavirus (HPV) DNA positive HPV (HPVDNA+) OSCC, suggesting an epidemic of viral-induced OSCC[1,2,3,4]. This may be of importance for the treatment of OSCC, where tonsillar squamous cell carcinoma (TSCC) and base of tongue squamous carcinoma (BOTSCC) dominate[5], since HPVDNA+ tumors have a much better clinical outcome than those that are HPV DNA negative (HPVDNA-)[6,7]. Since a significant proportion of patients with HPVDNA + OSCC have a poor clinical outcome, additional predictive markers are needed, before introducing a possible deescalation of treatment[9,10]

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