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Review ArticleClinical Review

Human Papillomavirus-Associated Head and Neck Cancer

Juan C. Nogues, Scott Fassas, Collin Mulcahy and Philip E. Zapanta
The Journal of the American Board of Family Medicine July 2021, 34 (4) 832-837; DOI: https://doi.org/10.3122/jabfm.2021.04.200588
Juan C. Nogues
From Division of Otolaryngology—Head and Neck Surgery, George Washington University, Washington, DC (JCN, SF, CM, PEZ).
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Scott Fassas
From Division of Otolaryngology—Head and Neck Surgery, George Washington University, Washington, DC (JCN, SF, CM, PEZ).
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Collin Mulcahy
From Division of Otolaryngology—Head and Neck Surgery, George Washington University, Washington, DC (JCN, SF, CM, PEZ).
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Philip E. Zapanta
From Division of Otolaryngology—Head and Neck Surgery, George Washington University, Washington, DC (JCN, SF, CM, PEZ).
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    Figure 1.

    SEER Age-Adjusted Trends in Oral Cavity and Pharynx Cancer, 1975 to 2017.1 Results from cancer incidence data from population-based cancer registries covering approximately 34.6% of the US population.

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    Figure 2.

    Human Papillomavirus (HPV) Prevalence Among Patients With Oropharyngeal Cancer as Reported in A Systematic Review and Meta-Analysis of Studies Published Between 1966 and 2010.7

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    Table 1.

    Proposed HPV Screening Tools12

    Screening ToolConceptLimitation
    Oral HPV screeningSample patient's saliva and test for high-risk HPV viral DNAAlthough this can detect the presence of HPV DNA, the majority of individuals will go on to clear the virus without progressing to carcinoma
    HPV serologyAsses serum levels of antibodies to high-risk HPV strandsSerum antibody levels represent the cumulative exposure to HPV but are not specific to exposure at a particular anatomic site (oropharynx, cervix, etc.) and do not reflect expression of HPV-related oncoproteins E6 and E7, which are necessary for carcinogenesis
    Transcervical ultrasoundUltrasound of the head and neck can be used to assess individuals with neck masses or those who are found to be at high risk via other screening methods. It may help detect small tumors in earlier stages and improve morbidityAlthough ultrasound is relatively inexpensive and can be done quickly in the office, it is not practical for universal screening and relies on either the symptom of a neck mass or other screening method to prescreen high-risk individuals
    Mucosal imagingDirect visualization of subclinical lesions via endoscopyThere are no identifiable premalignant lesions, and as with the limitations of ultrasound, there needs to be a prescreening method to identify high-risk individuals before subjecting them to this more invasive procedure. Additionally, many of these tumors arise from tonsillar crypts and cannot be easily identified on surface-level examination
    • HPV, Human papillomavirus; DNA, Deoxyribonucleic acid.

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    Table 2.

    Dosing Schedule of Gardasil 9 Vaccine as Recommended by Manufacturer16

    AgeNumber of DosesDosing Interval
    9 to 142 or 3Second dose 6-12 months after the first
    0, 2 months, 6 months
    15 to 4530, 2 months, 6 months
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The Journal of the American Board of Family     Medicine: 34 (4)
The Journal of the American Board of Family Medicine
Vol. 34, Issue 4
July/August 2021
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Human Papillomavirus-Associated Head and Neck Cancer
Juan C. Nogues, Scott Fassas, Collin Mulcahy, Philip E. Zapanta
The Journal of the American Board of Family Medicine Jul 2021, 34 (4) 832-837; DOI: 10.3122/jabfm.2021.04.200588

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Human Papillomavirus-Associated Head and Neck Cancer
Juan C. Nogues, Scott Fassas, Collin Mulcahy, Philip E. Zapanta
The Journal of the American Board of Family Medicine Jul 2021, 34 (4) 832-837; DOI: 10.3122/jabfm.2021.04.200588
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Keywords

  • Immunization
  • Otolaryngology
  • Papillomavirus Vaccines
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  • Primary Health Care
  • Sexually Transmitted Diseases
  • Squamous Cell Carcinoma of Head and Neck

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