Human papillomavirus and Epstein‐Barr virus co‐infection in oral and oropharyngeal squamous cell carcinomas: A systematic review and meta‐analysis

Author:

Rahman Rifat12,Shaikh Mushfiq H.3,Gopinath Divya4,Idris Adi15ORCID,Johnson Newell W.126

Affiliation:

1. Menzies Health Institute Queensland Griffith University Gold Coast Queensland Australia

2. School of Medicine and Dentistry Griffith University Gold Coast Queensland Australia

3. Department of Otolaryngology – Head and Neck Surgery Western University London Ontario Canada

4. Basic Medical and Dental Sciences Department College of Dentistry Ajman University Ajman United Arab Emirates

5. School of Biomedical Sciences Queensland University of Technology, Gardens Point Brisbane Queensland Australia

6. Faculty of Dentistry Oral and Craniofacial Sciences King's College London London UK

Abstract

AbstractSquamous cell carcinoma of the oral cavity (OSCC) is the most common head‐and‐neck malignancy. Importantly, we are experiencing an alarming rise in the incidence of oropharyngeal squamous cell carcinoma (OPSCC) globally. Oncogenic viruses, human papillomavirus (HPV) and Epstein‐Barr virus (EBV), are known to be co‐associated with OSCC and OPSCC cases. However, the reported incidence of HPV and EBV co‐infection in OSCCs and OPSCCs globally is unknown. To address this, we performed a formal meta‐analysis and systematic review on published studies that report the detection of both EBV and HPV in OSCCs and OPSCCs. Our analysis revealed 18 relevant studies out of a total of 1820 cases (1181 from the oral cavity and 639 from the oropharynx). Overall, HPV and EBV co‐infection was found in 11.9% of OSCC and OPSCC cases combined (95% CI: 8%–14.1%). Based on anatomical subsite, dual positivity estimates were 10.5% (95% CI: 6.7%–15.1%) for OSCC and 14.2% (95% CI: 9.1%–21.3%) for OPSCC. The highest dual positivity rates described were in European countries: for OSCC 34.7% (95% CI: 25.9%–44.6%) in Sweden and for OPSCC, 23.4% (95% CI: 16.9%–31.5%) in Poland. Given these substantive prevalence rates, the value of detecting dual infection in the diagnosis and prognosis of these cancers deserves careful longitudinal studies, as do implications for cancer prevention and therapy. We further proposed molecular mechanisms that could explain how HPV and EBV could co‐contribute to the aetiology of OSCCs and OPSCCs.

Publisher

Wiley

Subject

Microbiology (medical),General Dentistry,Immunology,Microbiology

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