Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal Cancer

The incidence of human papillomavirus (HPV)-positive oropharyngeal cancer (OPC) is rising in high-income countries, including Australia. Increasing evidence suggests that accurate HPV testing is pivotal for clinical decision making and treatment planning in these patients. Recently, the eighth editi...

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Main Authors: Kai Dun Tang, Kurt Baeten, Liz Kenny, Ian H. Frazer, Gert Scheper, Chamindie Punyadeera
Format: Article
Language:English
Published: MDPI AG 2019-04-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/11/4/473
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author Kai Dun Tang
Kurt Baeten
Liz Kenny
Ian H. Frazer
Gert Scheper
Chamindie Punyadeera
author_facet Kai Dun Tang
Kurt Baeten
Liz Kenny
Ian H. Frazer
Gert Scheper
Chamindie Punyadeera
author_sort Kai Dun Tang
collection DOAJ
description The incidence of human papillomavirus (HPV)-positive oropharyngeal cancer (OPC) is rising in high-income countries, including Australia. Increasing evidence suggests that accurate HPV testing is pivotal for clinical decision making and treatment planning in these patients. Recently, the eighth edition of the American Joint Committee on Cancer/Union for International Cancer Control (AJCC/UICC) tumor&#8211;node&#8211;metastasis (TNM) staging system for OPC (based on the p16INK4a (p16) status) was proposed and has been implemented. However, the applicability of this new staging system is still far from clear. In our study, <i>n</i> = 127 OPC patients from Queensland, Australia were recruited, and the tumor p16 expression in these patients was examined using immunohistochemical (IHC) analysis. HPV-16 genotyping, viral load, and physical status (episomal versus integrated) in the saliva samples of OPC patients were determined using the qPCR method. A good inter-rater agreement (<i>k</i> = 0.612) was found between tumor p16 expression and oral HPV-16 infection in OPC. Importantly, according to the eighth edition staging system, HPV-16 DNA viral load (&gt;10 copies/50 ng) was significantly associated with the advanced stages of OPC. In concordance with previous studies, a mixed HPV-16 form (partially or fully integrated) was predominately found in OPC patients. Taken together, our data support HPV-16 detection in saliva as a screening biomarker to identify people within the community who are at risk of developing OPC.
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spelling doaj.art-88c60bd53e094e8ebcfdc16001162e922023-09-02T23:53:09ZengMDPI AGCancers2072-66942019-04-0111447310.3390/cancers11040473cancers11040473Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal CancerKai Dun Tang0Kurt Baeten1Liz Kenny2Ian H. Frazer3Gert Scheper4Chamindie Punyadeera5The School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology and the Translational Research Institute, Queensland 4059, AustraliaJanssen Diagnostics, Janssen Pharmaceutica NV, Beerse 2340, BelgiumSchool of Medicine, University of Queensland, Queensland 4029, AustraliaFaculty of Medicine, The University of Queensland, Translational Research Institute, Queensland 4102, AustraliaJanssen Vaccines &amp; Prevention BV, Leiden 2333, The NetherlandsThe School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology and the Translational Research Institute, Queensland 4059, AustraliaThe incidence of human papillomavirus (HPV)-positive oropharyngeal cancer (OPC) is rising in high-income countries, including Australia. Increasing evidence suggests that accurate HPV testing is pivotal for clinical decision making and treatment planning in these patients. Recently, the eighth edition of the American Joint Committee on Cancer/Union for International Cancer Control (AJCC/UICC) tumor&#8211;node&#8211;metastasis (TNM) staging system for OPC (based on the p16INK4a (p16) status) was proposed and has been implemented. However, the applicability of this new staging system is still far from clear. In our study, <i>n</i> = 127 OPC patients from Queensland, Australia were recruited, and the tumor p16 expression in these patients was examined using immunohistochemical (IHC) analysis. HPV-16 genotyping, viral load, and physical status (episomal versus integrated) in the saliva samples of OPC patients were determined using the qPCR method. A good inter-rater agreement (<i>k</i> = 0.612) was found between tumor p16 expression and oral HPV-16 infection in OPC. Importantly, according to the eighth edition staging system, HPV-16 DNA viral load (&gt;10 copies/50 ng) was significantly associated with the advanced stages of OPC. In concordance with previous studies, a mixed HPV-16 form (partially or fully integrated) was predominately found in OPC patients. Taken together, our data support HPV-16 detection in saliva as a screening biomarker to identify people within the community who are at risk of developing OPC.https://www.mdpi.com/2072-6694/11/4/473human papillomavirusoropharyngeal cancersalivaHPV-16 viral loadHPV-16 integration
spellingShingle Kai Dun Tang
Kurt Baeten
Liz Kenny
Ian H. Frazer
Gert Scheper
Chamindie Punyadeera
Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal Cancer
Cancers
human papillomavirus
oropharyngeal cancer
saliva
HPV-16 viral load
HPV-16 integration
title Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal Cancer
title_full Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal Cancer
title_fullStr Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal Cancer
title_full_unstemmed Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal Cancer
title_short Unlocking the Potential of Saliva-Based Test to Detect HPV-16-Driven Oropharyngeal Cancer
title_sort unlocking the potential of saliva based test to detect hpv 16 driven oropharyngeal cancer
topic human papillomavirus
oropharyngeal cancer
saliva
HPV-16 viral load
HPV-16 integration
url https://www.mdpi.com/2072-6694/11/4/473
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