Abstract

BackgroundThe incidence of human papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OPSCC) has been rising in recent years. Given the clinical impact of HPV/p16 positivity in OPSCC, identifying surrogate markers of this disease early in the diagnostic work-up of these patients could improve patient care.MethodsDemographic, pathologic, staging and PET-CT data from patients diagnosed with OPSCC from 2009–2014 were obtained from a prospectively collected provincial cancer registry. Tumor HPV/p16 status was correlated to the maximum standard uptake value (SUVmax) of the primary tumor and cervical nodes. Comparisons of means and multinomial regression models were used to determine associations between p16 status and SUVmax. A diagnostic odds ratio was calculated using a cut off value for predicting HPV/p16 positivity based on nodal SUVmax.ResultsPET-CT and HPV/p16 data was obtained for 65 patients treated surgically for OPSCC. Significantly higher nodal SUVmax was associated with HPV/p16 positive nodes (SUVmax 10.8 vs 7.9). No significant differences were seen between HPV/p16 positive vs negative primary tumor SUVmax (10.3 vs 13.7). In combination with other clinical parameters, higher nodal SUVmax was highly correlated with HPV/p16 positivity.ConclusionElevated nodal SUVmax is a significant predictor of HPV/p16 positive disease.

Highlights

  • Oropharyngeal squamous cell carcinoma (OPSCC) is an aggressive malignancy with a rising incidence worldwide [1,2,3]

  • All adult patients treated with a primary surgical approach with a pre-treatment Positron emission tomography-computed tomography (PET-CT) and p16 status of the oropharyngeal squamous cell carcinoma (OPSCC) were included within the cohort (Fig. 1)

  • Of the patients treated with primary surgery, sixty-five had adequate pretreatment PET-CT and p16 status available (Fig. 1)

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Summary

Introduction

Oropharyngeal squamous cell carcinoma (OPSCC) is an aggressive malignancy with a rising incidence worldwide [1,2,3]. A large body of evidence from recent years has demonstrated that HPV positive and negative OPSCC are distinct from clinical, pathological and molecular perspectives [4, 6,7,8,9,10,11,12]. Most importantly; patients with HPV-related OPSCC, generally pathologically identified by p16 positivity, have favorable survival outcomes following both surgical and non-surgical. Rates of cervical lymph node metastases in HPV positive OPSCC have been reported to be 60-76 % at initial presentation [19]. The incidence of human papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OPSCC) has been rising in recent years. Given the clinical impact of HPV/p16 positivity in OPSCC, identifying surrogate markers of this disease early in the diagnostic work-up of these patients could improve patient care. Tumor HPV/p16 status was correlated to the maximum standard uptake value (SUVmax) of the primary tumor and cervical nodes. A diagnostic odds ratio was calculated using a cut off value for predicting HPV/p16 positivity based on nodal SUVmax

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