The Prevalence of Human Papillomavirus–Positive Oropharyngeal Squamous Cell Carcinoma at One of the Largest Tertiary Care Centers in Sub-Saharan Africa

Author:

Dapaah Gloria1,Hille Jos1,Faquin William C.2,Whittaker Judith3,Dittrich Corneli M.3,Ebrahim Abdul-Kader4,Schneider Johann W.5,van Wyk Abraham C.5,Opperman Johan1,Merven Marc4,Naidoo Komeela6,Loock James W.4,Afrogheh Amir H.1

Affiliation:

1. From the Department of Oral and Maxillofacial Pathology, National Health Laboratory Service, Tygerberg Academic Hospital, University of the Western Cape, Cape Town, South Africa (Dapaah, Hille, Opperman, Afrogheh)

2. the Pathology Service, Massachusetts General Hospital, Harvard Medical School, Boston (Faquin)

3. Lancet Laboratories, Cape Town, South Africa (Whittaker, Dittrich)

4. The Department of Ear, Nose and Throat (Ebrahim, Merven, Loock), Tygerberg Academic Hospital, University of Stellenbosch, Faculty of Medicine and Health Sciences, Cape Town, South Africa

5. Division of Anatomical Pathology, National Health Laboratory Service (Schneider, van Wyk), Tygerberg Academic Hospital, University of Stellenbosch, Faculty of Medicine and Health Sciences, Cape Town, South Africa

6. and the Division of Radiation Oncology, Department of Medical Imaging and Clinical Oncology (Naidoo), Tygerberg Academic Hospital, University of Stellenbosch, Faculty of Medicine and Health Sciences, Cape Town, South Africa

Abstract

Context.— Limited data exist on the prevalence of human papillomavirus (HPV)–positive oropharyngeal squamous cell carcinoma in sub-Saharan Africa. Objective.— To determine the prevalence of HPV-positive oropharyngeal squamous cell carcinoma at a large tertiary care center in South Africa. Design.— A total of 266 oropharyngeal squamous cell carcinomas diagnosed during an 11-year period (2007–2017) were selected for evaluation. Cases staining positive for p16 immunohistochemistry were evaluated for high-risk HPV using the BD Onclarity assay (BD Diagnostics, Sparks, Maryland). Results.— Of 266 oropharyngeal squamous cell carcinomas, 14% (n = 36) were positive for p16. Polymerase chain reaction for high-risk HPV performed on the p16-positive cases was negative in 23 cases and positive in 13 cases (13 of 266; 5%). p16 showed a positive predictive value of 36.1%. The HPV subtypes were HPV-16 (n = 10), HPV-18 (n = 1), HPV-52 (n = 1), and HPV-31 (n = 1). Human papillomavirus–positive cases occurred in 10 men and 3 women (mean age, 51 years) and arose from the tonsil (n = 10) or base of the tongue (n = 3). The HPV-positive cases were non-keratinizing (n = 10) or partially keratinizing (n = 1). Partially/nonkeratinizing cases revealed a modest improvement in p16 positive predictive value (11 of 21; 52.4%). Conclusions.— The presence of high-risk HPV in 5% of cases suggests that high-risk HPV is a minor etiologic agent in oropharyngeal squamous cell carcinoma in this region. Given its suboptimal positive predictive value, p16 is not a reliable marker for high-risk HPV infection in this region. When p16 is positive, HPV-specific testing is necessary. The identification of less common high-risk HPV types, HPV-52 and HPV-31, may influence current local vaccination strategies.

Publisher

Archives of Pathology and Laboratory Medicine

Subject

Medical Laboratory Technology,General Medicine,Pathology and Forensic Medicine

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