TY - JOUR
T1 - Prevalence of oral and blood oncogenic human papillomavirus biomarkers among an enriched screening population
T2 - Baseline results of the MOUTH study
AU - D’Souza, Gypsyamber
AU - Tewari, Sakshi R.
AU - Troy, Tanya
AU - Waterboer, Tim
AU - Struijk, Linda
AU - Castillo, Rachel
AU - Wright, Hannah
AU - Shen, Michael
AU - Miles, Brett
AU - Johansson, Mattias
AU - Robbins, Hilary A.
AU - Fakhry, Carole
N1 - Funding Information:
We thank the HPV Cancer Cohort Consortium for sharing data on sex-specific HPV seroprevalence and Maura Gillison and Anil Chaturvedi for oral HPV testing performed in the NHANES and used as publicly available data for this analysis. This study was supported by grant/contract R35DE026631 from the National Institute of Dental and Craniofacial Research/National Institutes of Health and by grant/contract 5U01CA195603 from the National Cancer Institute. Where authors are identified as personnel of the International Agency for Research on Cancer/World Health Organization, the authors alone are responsible for the views expressed in this article and do not necessarily represent the decisions, policies, or views of the International Agency for Research on Cancer/World Health Organization.
Funding Information:
We thank the HPV Cancer Cohort Consortium for sharing data on sex‐specific HPV seroprevalence and Maura Gillison and Anil Chaturvedi for oral HPV testing performed in the NHANES and used as publicly available data for this analysis. This study was supported by grant/contract R35DE026631 from the National Institute of Dental and Craniofacial Research/National Institutes of Health and by grant/contract 5U01CA195603 from the National Cancer Institute. Where authors are identified as personnel of the International Agency for Research on Cancer/World Health Organization, the authors alone are responsible for the views expressed in this article and do not necessarily represent the decisions, policies, or views of the International Agency for Research on Cancer/World Health Organization.
Publisher Copyright:
© 2023 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.
PY - 2023/8/1
Y1 - 2023/8/1
N2 - Background: Human papillomavirus (HPV)-related oropharyngeal cancer screening is being explored in research studies, but strategies to identify an appropriate population are not established. The authors evaluated whether a screening population could be enriched for participants with oncogenic HPV biomarkers using risk factors for oral HPV. Methods: Participants were enrolled at Johns Hopkins Hospitals and Mount Sinai Icahn School of Medicine. Eligible participants were either men aged 30 years or older who had two or more lifetime oral sex partners and a personal history of anogenital dysplasia/cancer or partners of patients who had HPV-related cancer. Oral rinse and serum samples were tested for oncogenic HPV DNA, RNA, and E6 or E7 antibodies, respectively. Participants with any biomarker were considered at-risk. Results: Of 1108 individuals, 7.3% had any oncogenic oral HPV DNA, and 22.9% had serum antibodies for oncogenic HPV E6 or E7. Seventeen participants (1.5%) had both oral and blood biomarkers. HPV type 16 (HPV16) biomarkers were rarer, detected in 3.7% of participants, including 20 with oral HPV16 DNA and 22 with HPV16 E6 serum antibodies (n = 1 had both). In adjusted analysis, living with HIV (adjusted odds ratio, 2.65; 95% CI, 1.60–4.40) and older age (66–86 vs. 24–45 years; adjusted odds ratio, 1.70; 95% CI, 1.07–2.70) were significant predictors of being at risk. Compared with the general population, the prevalence of oral HPV16 (1.8% vs. 0.9%), any oncogenic oral HPV DNA (7.3% vs. 3.5%), and HPV16 E6 antibodies (2.2% vs. 0.3%) was significantly elevated. Conclusions: Enrichment by the eligibility criteria successfully identified a population with higher biomarker prevalence, including HPV16 biomarkers, that may be considered for screening trials. Most in this group are still expected to have a low risk of oropharyngeal cancer.
AB - Background: Human papillomavirus (HPV)-related oropharyngeal cancer screening is being explored in research studies, but strategies to identify an appropriate population are not established. The authors evaluated whether a screening population could be enriched for participants with oncogenic HPV biomarkers using risk factors for oral HPV. Methods: Participants were enrolled at Johns Hopkins Hospitals and Mount Sinai Icahn School of Medicine. Eligible participants were either men aged 30 years or older who had two or more lifetime oral sex partners and a personal history of anogenital dysplasia/cancer or partners of patients who had HPV-related cancer. Oral rinse and serum samples were tested for oncogenic HPV DNA, RNA, and E6 or E7 antibodies, respectively. Participants with any biomarker were considered at-risk. Results: Of 1108 individuals, 7.3% had any oncogenic oral HPV DNA, and 22.9% had serum antibodies for oncogenic HPV E6 or E7. Seventeen participants (1.5%) had both oral and blood biomarkers. HPV type 16 (HPV16) biomarkers were rarer, detected in 3.7% of participants, including 20 with oral HPV16 DNA and 22 with HPV16 E6 serum antibodies (n = 1 had both). In adjusted analysis, living with HIV (adjusted odds ratio, 2.65; 95% CI, 1.60–4.40) and older age (66–86 vs. 24–45 years; adjusted odds ratio, 1.70; 95% CI, 1.07–2.70) were significant predictors of being at risk. Compared with the general population, the prevalence of oral HPV16 (1.8% vs. 0.9%), any oncogenic oral HPV DNA (7.3% vs. 3.5%), and HPV16 E6 antibodies (2.2% vs. 0.3%) was significantly elevated. Conclusions: Enrichment by the eligibility criteria successfully identified a population with higher biomarker prevalence, including HPV16 biomarkers, that may be considered for screening trials. Most in this group are still expected to have a low risk of oropharyngeal cancer.
KW - antibody
KW - biomarker
KW - human papillomavirus (HPV)
KW - oral sex
KW - oropharyngeal cancer (OPC)
KW - screening
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U2 - 10.1002/cncr.34783
DO - 10.1002/cncr.34783
M3 - Article
C2 - 37032449
AN - SCOPUS:85152249974
SN - 0008-543X
VL - 129
SP - 2373
EP - 2384
JO - Cancer
JF - Cancer
IS - 15
ER -