Abstract

Although HPV-positive oropharyngeal cancer (OPC) patients have improved prognosis compared to HPV negative patients; there remains an HPV-positive group who have poor outcomes. Biomarkers to stratify discrete patient outcomes are thus desirable. Our objective was to analyse viral load (VL) by droplet digital PCR (ddPCR), in HPV-positive patients with OPC on whom clinical outcome data were available. In a cohort of patients that had previously tested HPV positive via conventional PCR, VL was determined using ddPCR assays for HPV16 L1 and E6 genes. VL was classed as "medium/high" if more than 5.57 copies or 8.68 copies of the HPV 16 L1 or E6 gene were detected respectively. Effect of VL on overall survival and hazard of death & disease progression was performed with adjustments made for sex, age, deprivation, smoking, alcohol consumption and stage. L1 VL ranged from 0.0014-304 gene copies per cell with a mean of 30.9; comparatively E6 VL ranged from 0.0012-356 copies per cell with a mean of 37.9. Univariate analysis showed those with a medium/high VL had a lower hazard of death; this was significant for L1 (p = 0.02) but not for E6 (p = 0.67). The ratio of E6 to L1 deviated from n = 1 in most samples but had no influence on clinical outcomes. HPV viral load may be informative for the further stratification of clinical outcomes in HPV positive OPC patients.

Highlights

  • The incidence of oropharyngeal cancer (OPC) has increased dramatically over the last two decades including in the United Kingdom [1,2]

  • While the extent of HPV driven OPC varies, data converge on the fact that HPV positive status is independently associated with better clinical outcomes [4,5]

  • This has led to a recent change in tumour classification which incorporates HPV status and trials to determine the efficacy of de-escalated therapy in HPV positive OPC patients [6,7]

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Summary

Introduction

The incidence of oropharyngeal cancer (OPC) has increased dramatically over the last two decades including in the United Kingdom [1,2]. While the extent of HPV driven OPC varies, data converge on the fact that HPV positive (versus negative) status is independently associated with better clinical outcomes [4,5]. This has led to a recent change in tumour classification which incorporates HPV status and trials to determine the efficacy of de-escalated therapy in HPV positive OPC patients [6,7]. Results: L1 VL ranged from 0.0014–304 gene copies per cell with a mean of 30.9; comparatively E6 VL ranged from 0.0012–356 copies per cell with a mean of 37.9 Univariate analysis showed those with a medium/high VL had a lower hazard of death; this was significant for L1 (p = 0.02) but not for E6 (p = 0.67). Conclusions: HPV viral load may be informative for the further stratification of clinical outcomes in HPV positive OPC patients

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