Role of Human Papillomavirus Infection in Head and Neck Cancer in Italy: The HPV-AHEAD Study

Simple Summary This is the largest and most comprehensive assessment of the role of human papillomavirus (HPV) in head and neck cancer (HNC) in Italy, which is a region currently considered bearing a low burden of HPV-driven HNC. p16INK4a, HPV-DNA, and HPV RNA biomarkers were used to assess the HPV status in head and neck cancer in a retrospective cohort of approximately 700 patients. In our study, HPV prevalence in oropharyngeal cancers was much higher than in oral and laryngeal cancers, and HPV positivity conferred better prognosis only in oropharyngeal cancers. Importantly, we have observed an increase of the prevalence of HPV positivity in oropharyngeal cancers in the most recent calendar periods, suggesting that this disease is increasing in Italy, as has happened before in other developed regions. Abstract Literature on the role of human papillomavirus (HPV) in head and neck cancer (HNC) in Italy is limited, especially for non-oropharyngeal tumours. Within the context of the HPV-AHEAD study, we aimed to assess the prognostic value of different tests or test algorithms judging HPV carcinogenicity in HNC and factors related to HPV positivity at the European Institute of Oncology. We conducted a retrospective cohort study (2000–2010) on a total of 696 primary HNC patients. Formalin-fixed, paraffin-embedded cancer tissues were studied. All HPV-DNA-positive and a random sample of HPV-DNA-negative cases were subjected to HPV-E6*I mRNA detection and p16INK4a staining. Multivariate models were used to assess for factors associated with HPV positivity and proportional hazards for survival and recurrence. The percentage of HPV-driven cases (considering HPV-E6*I mRNA positivity) was 1.8, 2.2, and 40.4% for oral cavity (OC), laryngeal (LC), and oropharyngeal (OPC) cases, respectively. The estimates were similar for HPV-DNA/p16INK4a double positivity. Being a non-smoker or former smoker or diagnosed at more recent calendar periods were associated with HPV-E6*I mRNA positivity only in OPC. Being younger was associated with HPV-E6*I mRNA positivity in LC. HPV-driven OPC, but not HPV-driven OC and LC, showed better 5 year overall and disease-free survival. Our data show that HPV prevalence in OPC was much higher than in OC and LC and observed to increase in most recent years. Moreover, HPV positivity conferred better prognosis only in OPC. Novel insights on the role of HPV in HNC in Italy are provided, with possible implications in the clinical management of these patients.

[1]  Age-independent increasing prevalence of Human Papillomavirus-driven oropharyngeal carcinomas in North-East Italy , 2020, Scientific Reports.

[2]  L. Chow Head and Neck Cancer. , 2020, The New England journal of medicine.

[3]  J. Ferlay,et al.  Global burden of cancer attributable to infections in 2018: a worldwide incidence analysis. , 2019, The Lancet. Global health.

[4]  K. Higgins,et al.  National treatment trends in human papillomavirus–positive oropharyngeal squamous cell carcinoma , 2019, Cancer.

[5]  M. Diefenbach,et al.  Alcohol‐related head and neck cancer: Summary of the literature , 2019, Head & neck.

[6]  B. Burkey,et al.  Impact of active smoking on outcomes in HPV+ oropharyngeal cancer , 2019, Head & neck.

[7]  S. Chiocca,et al.  Human papillomavirus as a driver of head and neck cancers , 2019, British Journal of Cancer.

[8]  F. Bussu,et al.  HPV as a marker for molecular characterization in head and neck oncology: Looking for a standardization of clinical use and of detection method(s) in clinical practice , 2019, Head & neck.

[9]  C. Tinelli,et al.  The evolving landscape of human papillomavirus-related oropharyngeal squamous cell carcinoma at a single institution in Northern Italy , 2019, Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale.

[10]  W. Yarbrough,et al.  Association of Human Papillomavirus Status at Head and Neck Carcinoma Subsites With Overall Survival , 2018, JAMA otolaryngology-- head & neck surgery.

[11]  Ruud H. Brakenhoff,et al.  The molecular landscape of head and neck cancer , 2018, Nature Reviews Cancer.

[12]  S. de Sanjosé,et al.  Double positivity for HPV-DNA/p16ink4a is the biomarker with strongest diagnostic accuracy and prognostic value for human papillomavirus related oropharyngeal cancer patients. , 2018, Oral oncology.

[13]  M. Rugge,et al.  The evolution of the epidemiological landscape of head and neck cancer in Italy: Is there evidence for an increase in the incidence of potentially HPV-related carcinomas? , 2018, PloS one.

[14]  Carol Colasacco,et al.  Human Papillomavirus Testing in Head and Neck Carcinomas: Guideline From the College of American Pathologists. , 2017, Archives of pathology & laboratory medicine.

[15]  S. de Sanjosé,et al.  Development and validation of a protocol for optimizing the use of paraffin blocks in molecular epidemiological studies: The example from the HPV-AHEAD study , 2017, PloS one.

[16]  L. Alemany,et al.  Human papillomavirus-related oropharyngeal cancer , 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

[17]  S. Khariwala,et al.  Tobacco-related carcinogenesis in head and neck cancer , 2017, Cancer and Metastasis Reviews.

[18]  P. Brennan,et al.  Role of mucosal high‐risk human papillomavirus types in head and neck cancers in central India , 2017, International journal of cancer.

[19]  B. O'Sullivan,et al.  Overview of the 8th Edition TNM Classification for Head and Neck Cancer , 2017, Current Treatment Options in Oncology.

[20]  R. Decker,et al.  A Comparison of Prognostic Ability of Staging Systems for Human Papillomavirus–Related Oropharyngeal Squamous Cell Carcinoma , 2017, JAMA oncology.

[21]  M. von Knebel Doeberitz,et al.  Diagnostic accuracy of p16INK4a immunohistochemistry in oropharyngeal squamous cell carcinomas: A systematic review and meta‐analysis , 2017, International journal of cancer.

[22]  M. Pawlita,et al.  Low prevalence of HPV-driven head and neck squamous cell carcinoma in North-East Italy , 2016, Papillomavirus research.

[23]  R. Malekzadeh,et al.  Mucosal alpha‐papillomaviruses are not associated with esophageal squamous cell carcinomas: Lack of mechanistic evidence from South Africa, China and Iran and from a world‐wide meta‐analysis , 2016, International journal of cancer.

[24]  M. Poljak,et al.  HPV Involvement in Head and Neck Cancers: Comprehensive Assessment of Biomarkers in 3680 Patients. , 2016, Journal of the National Cancer Institute.

[25]  S. Nuyts,et al.  HPV Positive Head and Neck Cancers: Molecular Pathogenesis and Evolving Treatment Strategies , 2016, Cancers.

[26]  M. Lenarz,et al.  Meta-analysis of survival in patients with HNSCC discriminates risk depending on combined HPV and p16 status , 2016, European Archives of Oto-Rhino-Laryngology.

[27]  Carole Fakhry,et al.  Epidemiology of Human Papillomavirus-Positive Head and Neck Squamous Cell Carcinoma. , 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[28]  M. Poljak,et al.  Human papillomavirus DNA prevalence and type distribution in anal carcinomas worldwide , 2015, International journal of cancer.

[29]  Jacques Ferlay,et al.  Worldwide trends in incidence rates for oral cavity and oropharyngeal cancers. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[30]  S. Franceschi,et al.  Biological activity of probable/possible high‐risk human papillomavirus types in cervical cancer , 2013, International journal of cancer.

[31]  L. Alemany,et al.  Human papillomavirus and diseases of the upper airway: head and neck cancer and respiratory papillomatosis. , 2012, Vaccine.

[32]  Y. Qiao,et al.  EUROGIN 2011 roadmap on prevention and treatment of HPV‐related disease , 2012, International journal of cancer.

[33]  M. Pawlita,et al.  Viral RNA patterns and high viral load reliably define oropharynx carcinomas with active HPV16 involvement. , 2012, Cancer research.

[34]  D. Rickman,et al.  Biological and clinical relevance of transcriptionally active human papillomavirus (HPV) infection in oropharynx squamous cell carcinoma , 2010, International journal of cancer.

[35]  M. Pawlita,et al.  Abundance of Multiple High-Risk Human Papillomavirus (HPV) Infections Found in Cervical Cells Analyzed by Use of an Ultrasensitive HPV Genotyping Assay , 2009, Journal of Clinical Microbiology.

[36]  S. Franceschi,et al.  Prevalence of human papillomavirus types in cervical and oral cancers in central India. , 2009, Vaccine.

[37]  A. Cmelak,et al.  Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trial. , 2008, Journal of the National Cancer Institute.

[38]  S. Franceschi,et al.  Development of a Sensitive and Specific Assay Combining Multiplex PCR and DNA Microarray Primer Extension To Detect High-Risk Mucosal Human Papillomavirus Types , 2006, Journal of Clinical Microbiology.