Abstract

BackgroundThe etiological role of human papillomavirus (HPV) in oropharyngeal squamous cell carcinoma (OPSCC) is confirmed. However, the role of other oncoviruses in OPSCC is unknown.Materials and methodsA total of 158 consecutive OPSCC patients treated with curative intent were included. DNA extracted from tumor sections was used to detect Epstein–Barr virus (EBV), HPV, and the following polyomaviruses: John Cunningham virus (JCV), Simian virus 40 (SV40), and BK virus (BKV) with PCR. In addition, p16 expression was studied by immunohistochemistry, and EBV-encoded small RNA (EBER) transcripts were localized by in situ hybridization. The effect of viral status on overall survival (OS) and disease-free survival (DFS) was analyzed.ResultsA total of 94/158 samples (59.5%) were HPV-positive, 29.1% contained BKV DNA, 20.3% EBV DNA, 13.9% JCV DNA, and 0.6% SV40 DNA. EBER was expressed only in stromal lymphocytes adjacent to the tumor and correlated with HPV positivity (p = 0.026). p16 expression associated only with HPV. None of the three polyomaviruses had an impact on survival. Patients with EBER-positive but HPV-negative OPSCC had significantly poorer OS and DFS than those with HPV-positive OPSCC and slightly worse prognosis compared with the patients with EBER-negative and HPV-negative OPSCC.ConclusionPolyomaviruses are detectable in OPSCC but seem to have no impact on survival, whereas HPV was the strongest viral prognostic factor. EBER expression, as a sign of latent EBV infection, may have prognostic impact among patients with HPV-negative OPSCC. EBER analysis may identify a new subgroup of OPSCCs unrelated to HPV.

Highlights

  • Several viruses have been detected in head and neck squamous cell carcinoma (HNSCC) [1,2,3,4,5,6,7]

  • We investigated the presence of human papillomavirus (HPV) and other oncoviruses including Epstein–Barr virus (EBV) and polyomaviruses (JCV, BK virus (BKV), and Simian virus 40 (SV40)) and their association with clinicopathological variables in an oropharyngeal squamous cell carcinoma (OPSCC) patient series

  • We showed that polyomaviruses are detectable in OPSCC but seem to have no association with clinicopathological features or prognosis

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Summary

Introduction

Several viruses have been detected in head and neck squamous cell carcinoma (HNSCC) [1,2,3,4,5,6,7] Their etiologic and prognostic role is of great interest in cancer prevention and new management practices including immunotherapy [8,9,10] and treatment de-escalation [11,12,13]. The etiological role of human papillomavirus (HPV) in oropharyngeal squamous cell carcinoma (OPSCC) is confirmed. Conclusion Polyomaviruses are detectable in OPSCC but seem to have no impact on survival, whereas HPV was the strongest viral prognostic factor. EBER expression, as a sign of latent EBV infection, may have prognostic impact among patients with HPV-negative OPSCC. EBER analysis may identify a new subgroup of OPSCCs unrelated to HPV

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