Accuracy of p16 IHC in Classifying HPV-Driven OPSCC in Different Populations

Author:

Gallus Roberto1,Nauta Irene H2ORCID,Marklund Linda345ORCID,Rizzo Davide6ORCID,Crescio Claudia7ORCID,Mureddu Luca8,Tropiano Paolo7ORCID,Delogu Giovanni910,Bussu Francesco6ORCID

Affiliation:

1. Otolaryngology, Mater Olbia Hospital, 07026 Olbia, Italy

2. Amsterdam UMC, Vrije Universiteit Amsterdam, Otolaryngology/Head and Neck Surgery, Cancer Center, 1081 Amsterdam, The Netherlands

3. Department of Clinical Science, Intervention and Technology, Department of Oto-Rhinolaryngology, Head and Neck Surgery, Karolinska University Hospital, Karolinska Institute, 17164 Stockholm, Sweden

4. Medical Unit Head Neck, Lung and Skin Cancer, Karolinska University Hospital, 17164 Stockholm, Sweden

5. Department of Surgical Sciences, Section of Otolaryngology and Head and Neck Surgery, Uppsala University, 75105 Uppsala, Sweden

6. Otolaryngology Division, Department of Medical, Surgical and Experimental Sciences, University of Sassari, Viale San Pietro, 43, 07100 Sassari, Italy

7. Otolaryngology Division, Azienda Ospedaliera Universitaria, 07100 Sassari, Italy

8. U.O.C. Otorinolaringoiatria, Università degli Studi di Cagliari, Policlinico Universitario Duilio Casula, 09042 Monserrato, Italy

9. Dipartimento di Scienze Biotecnologiche di Base, Cliniche Intensivologiche e Perioperatorie (Sezione di Microbiologia), Università Cattolica del Sacro Cuore, 00168 Roma, Italy

10. Mater Olbia Hospital, 07026 Olbia, Italy

Abstract

High-risk human papillomavirus (HPV) infection is a defined etiopathogenetic factor in oropharyngeal carcinogenesis with a clear prognostic value. The P16 IHC (immunohistochemistry) is a widely accepted marker for HPV-driven carcinogenesis in oropharyngeal squamous cell carcinoma (OPSCC); in the present paper, we discuss its reliability as a standalone marker in different populations. The literature suggests that rates of p16 IHC false positive results are inversely correlated with the prevalence of HPV-driven carcinogenesis in a population. We propose a formula that can calculate such a false positive rate while knowing the real prevalence of HPV-driven OPSCCs in a given population. As it has been demonstrated that p16 positive/HPV negative cases (i.e., false positives at p16 IHC) have the same prognosis as p16 negative OPSCC, we conclude that despite the valuable prognostic value of p16 IHC, relying only on a p16 IHC positive result to recommend treatment de-intensification could be risky. For this aim, confirmation with an HPV nucleic acid detection system, especially in areas with a low prevalence of HPV-related OPSCCs, should be pursued.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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