Cancer (Head and Neck)

Key Points

  • Although they border each other, the oral cavity (OC) and oropharynx (OP) are separate, non-overlapping anatomic regions.
  • Squamous cell carcinoma (SCC) is the most common malignancy in the OC and OP, accounting for 90% of cancers of the head and neck.
  • OC and OP cancers account for 2.8% of all cancers diagnosed in the U.S. and 1.8% of all cancer deaths. 
  • The 5-year relative survival rate for those with localized disease at diagnosis is 85%, compared with only 40% in patients whose cancer has metastasized.
  • The major risk factors for OC-SCC and OP-SCC are tobacco use, alcohol consumption, interaction between heavy use of tobacco and alcohol together, and chewing betel quid (“paan,” often practiced in Asian, migrant Asian, and other communities). Infection with human papillomavirus (HPV) is a major risk factor for oropharyngeal cancer, rather than oral cancer.
  • The National Institute for Dental and Craniofacial Research (NIDCR) provides an oral cancer examination protocol for dental practitioners.
Introduction

Squamous cell carcinomas of the head and neck collectively refer to cancers arising from the squamous cell layer of the mucosal surfaces in the oral cavity and oropharynx.1 Head and neck cancers can also begin in the salivary glands, paranasal sinuses or nasal cavity, but are relatively uncommon.1 Although they border each other, the oral cavity (OC) and oropharynx (OP) are separate, non-overlapping anatomic regions (Table; Figure).2, 3

Table. Anatomic Distinctions Between the Oral Cavity and the Oropharynx

Oral Cavity (OC)

Oropharynx (OP)

Anatomic border between from above: Junction of the hard and soft palate

Hard palate

Soft palate

Retromolar trigone

Palatine tonsils

Floor of the mouth

Palatoglossal folds

Anterior two-thirds of the tongue (i.e., anterior to the circumvallate papillae)

Posterior one-third of the tongue (i.e., base of the tongue)

Alveolar ridge and gingiva

Valleculae

Buccal mucosa

Posterior pharyngeal wall

Labial mucosa

 

Anatomic border between from below: Circumvallate papillae


  

Diagram of the side of a human head indicating the locations of various regions of the oropharynx

Diagram of the oral cavity and oropharynx from the Centers for Disease Control and Prevention

Incidence and Mortality

Squamous cell carcinoma (SCC) is the most common malignancy in the OC and pharynx, accounting for 90% of cancers of the head and neck, after excluding non-melanoma skin cancers.2 The American Cancer Society’s estimated number of new OC and pharynx cancer cases in the U.S. in 2022 is 54,000, while the estimated number of deaths from oral cavity and pharyngeal cancers in 2022 is 11,230.4 These estimates account for 2.8% of all cancers diagnosed and 1.8% of all cancer deaths, with over twice the number of new oral cavity and pharyngeal cancer cases and cancer deaths projected to occur in men than in women.4

Data from the National Cancer Institute’s Surveillance, Epidemiology and End Results (SEER) Program indicate that, from 2009 to 2018, there was a statistically significant annual percentage increase in the incidence of squamous cell carcinoma of the tongue (1.5%), tonsil (1.7%) and oropharynx (4.2%); and a decrease in the annual percent change in incidence of cancer of the lip (down 1.9%), floor of the mouth  (down 3.8%) and hypopharynx (down 2.7%).5

According to a 2022 study, the most common subsite of OC-SCC in the U.S. is the tongue (41.7%), and the overall incidence of oral tongue SCC has steadily increased among American men and women of all ages, with an average annual percentage increase of 1.8%.6 The 5-year relative survival rate for those with localized oral cavity or pharynx cancer at diagnosis is 85%, compared with only 40% in patients whose cancer has metastasized.7

Risk Factors

The major risk factors for OC-SCC and OP-SCC are tobacco use,2, 8-10 alcohol consumption,2, 8, 11-14 interaction between heavy use of tobacco and alcohol together,15, 16 and chewing betel quid (“paan,” often practiced in Asian, migrant Asian, and other communities).2  Human papillomavirus (HPV) infection is a major risk factor for oropharyngeal cancer and is also a risk factor for a small percentage of cancers at other anatomic sites of the head and neck (see following section “Focus on HPV in Oropharyngeal Cancer”).2, 17-21 A 2016 study reported that nearly 37 percent of oral cavity and pharyngeal cancer cases are attributable to alcohol consumption, with higher risks reported among moderate to heavy drinkers of alcohol.22

Ultraviolet exposure may be the likely risk factor associated with SCC of the lip.23 In the United States, male adults in older age groups have been reported to have increased risk of OC/OP-SCC.24 Smoking-associated risk appears to be dose dependent and correlates with daily or cumulative cigarette consumption.2 For patients who quit smoking, the risk for OC-SCC and OP-SCC declines over time and may approach that of nonsmokers after 10 or more years of cessation.2, 10, 25 The risk of head and neck cancer 20 or more years following cessation of alcohol consumption appears to approach the risk of those who have never consumed alcohol.26

Oncogenic oral HPV infection (especially HPV-16) has been established as an etiologic risk factor for HPV-positive oropharyngeal cancer.2, 17, 18, 27 In the U.S., approximately 3.5 percent of adults have been estimated to have oncogenic oral HPV infection, and the prevalence of this type of infection was most prevalent among adult men who currently smoked and men who reported a greater number of lifetime oral sexual partners.28, 29

Researchers have reported an increasing incidence of oral tongue SCC in the United States30 and globally,31 including a 2.3% increase of oral tongue SCC among women.6 The reported increase in oral tongue SCC has been suggested to have a different causative mechanism (e.g., genetic abnormalities such as Fanconi anemia, other oncogenic viral infections, or other environmental exposures).32 There is also an increased risk for OC/OP-SCC in patients with certain rare heritable conditions, including Fanconi anemia, dyskeratosis congenita, and Bloom syndrome.2 33

The HPV vaccine was developed to prevent cervical and other cancers of the reproductive system. The vaccine protects against the types of HPV that can cause oropharyngeal cancers, so it may also prevent oropharyngeal cancers; however, studies have not been done to show this.34

Focus on HPV

Oncogenic oral HPV infection is a major risk factor for oropharyngeal cancer, rather than oral cancer, per se.2, 17, 18, 27, 35, 36  HPV has emerged as an etiologic factor for OP-SCC of the tonsil and oropharynx,18, 35, 37 but not for the totality of tongue cancers.38, 39  Based on data from U.S. cancer registries, an estimated 71% of OP-SCC each year—or over 11,000 cases—are associated with HPV infection.40, 41 The vast majority (over 90%) of HPV-positive OP-SCC are associated with HPV-16, a high-risk, HPV subtype that is commonly associated with cervical cancer and other anogenital cancers.18, 37, 42, 43

Oropharyngeal cancer is now considered the most common cancer caused by HPV in the United States, with nearly 81 percent of OP-SCC cases classified as HPV-associated (between 2007 and 2015).44 Three analyses of U.S. cancer databases over two time periods (2013-2014 and 2017-2018) indicated that white, non-Hispanic men have higher incidences of oral cavity and pharyngeal cancers in the U.S.21, 45, 46 Another study found that the median age of individuals diagnosed with HPV-associated OP-SCC in the U.S. has increased to about 58 years of age, with a growing number of cases across all age groups, including older adults.47

Data suggest that oral HPV infection prevalence is lower in men and women who have received HPV vaccination than those who have not.48 Although it is possible that the HPV vaccine might also ultimately prevent OP cancers, as the vaccine prevents an initial infection with HPV types that can cause these cancers, current data are lacking regarding prevention of HPV-associated OP cancer.34 Clinical trials designed to answer these questions are currently underway.

HPV Vaccine

In 2020, the American Academy of Pediatric Dentistry (AAPD) issued an updated policy statement on HPV vaccination49  as follows:

The AAPD supports measures that prevent [oral and oropharyngeal cancers], including the prevention of HPV infection, a critical factor in the development of oral squamous cell carcinoma.

The AAPD encourages oral health care providers to:

  • Educate patients, parents, and guardians on the serious health consequences of [oral and oropharyngeal cancers] and the relationship of HPV to [oral and oropharyngeal cancers].
  • Counsel patients, parents, and guardians regarding the HPV vaccination, in accordance with CDC recommendations, as part of anticipatory guidance for adolescent patients. 

In October 2018, the U.S. Food and Drug Administration (FDA) approved a supplemental application for Gardasil 9® (HPV 9 valent-vaccine, recombinant; Merck & Co., Inc.) expanding the approved use of the vaccine to include women and men aged 27 through 45 years.50 Gardasil 9® was previously approved for use in males and females aged 9 through 26 years.

In 2020, Villa et al.51 published an umbrella review of systematic reviews, summarizing evidence on the safety, efficacy, and effectiveness of HPV vaccines.  The review compiled findings from 30 systematic reviews and found evidence that available HPV vaccines “are safe, effective, and efficacious against vaccine-type HPV infection and HPV-associated cellular changes, including precancerous and benign lesions.”
Signs and Symptoms

Two oral lesions that could be precursors to cancer are leukoplakia (white patches) and erythroplakia (red patches).2, 52 Although there is a known potential for malignant transformation, the majority of leukoplakias will not progress to cancer.2  Some oral lesions will show a combination of red and white features, termed erythroleukoplakia, speckled leukoplakia, or speckled erythroplakia.2 Although less common than leukoplakia, erythroplakia and lesions with erythroplakic components have a much greater potential for becoming cancerous.52

Because these white and/or red mucosal patches have an increased risk of becoming or already harboring invasive carcinoma, they have collectively been classified as “oral potentially malignant disorders.”33 Any white or red patch/lesion that does not resolve in two weeks should be reevaluated and considered for biopsy to obtain a definitive diagnosis. 52

Other possible signs and symptoms of head and neck cancers that patients may report include: 52

  • a lump or thickening in the oral soft tissues
  • soreness or a feeling that something is caught in the throat
  • difficulty chewing or swallowing
  • ear pain
  • difficulty moving the jaw or tongue
  • hoarseness
  • numbness of the tongue or other areas of the mouth
  • swelling of the jaw that causes dentures to fit poorly or become uncomfortable

Signs and symptoms that persist for two weeks or more merit further investigation, such as a biopsy or referral to a specialist.52

OP-SCC develops primarily in the palatine tonsils and base of the tongue, often appearing as an ulcerated mass, fullness, or irregular erythematous mucosal change.2, 53 OP-SCC tumors are thought to present at a more advanced stage than OC-SCC because of their ability to grow undetected (i.e., without overt symptoms) and their propensity for metastasis.2 The most common chief complaints are presence of a neck mass (from metastatic disease), sore throat, and dysphagia.2

Disease Detection

In 2017, an expert panel convened by the American Dental Association (ADA) Council on Scientific Affairs published a systematic review/meta-analysis and guideline titled "Evidence-Based Clinical Practice Guideline for the Evaluation of Potentially Malignant Disorders in the Oral Cavity.”54, 55 The goal of this clinical practice guideline is to inform clinicians about the potential use of adjuncts as triage tools for the evaluation of lesions, including potentially malignant disorders, in the oral cavity. Among the guideline's recommendations:

  • Clinicians should obtain an updated medical, social, and dental history and perform an intraoral and extraoral conventional visual and tactile examination in all adult patients.
  • For patients with suspicious lesions, clinicians should immediately perform a biopsy of the lesion or refer the patient to a specialist.
  • Salivary and light-based adjuncts are not recommended for evaluating lesions for malignancy. 

The U.S. Preventive Services Task Force (USPSTF)56 concluded in 2013 that “current evidence is insufficient to assess the balance of benefits and harms of screening for oral cancer in asymptomatic adults,” although the statement specifically clarifies that, “This recommendation is intended for primary care providers and does not pertain to dental providers or otolaryngologists. Dental care providers and otolaryngologists may conduct a comprehensive examination of the oral cavity and pharynx during the clinical encounter.”

ADA Current Dental Terminology (CDT) code D0120 for “periodic oral evaluation” (established patient) includes “an oral cancer evaluation … where indicated.” CDT code D0150 for “comprehensive oral evaluation” (new or established patient) also includes “an evaluation for oral cancer where indicated.”

The National Institute for Dental and Craniofacial Research (NIDCR)52 provides a protocol for dental practitioners for an oral cancer examination based on the standardized oral examination method recommended by the World Health Organization. The NIDCR examination method is “consistent with those followed by the Centers for Disease Control and Prevention and the National Institutes of Health,” and requires adequate lighting, a dental mouth mirror, two 2" x 2" gauze squares, and gloves, and should take approximately 5 minutes.52 The NIDCR provides the examination protocol in poster form and also has a pamphlet on oral cancer for patients and a patient education resource for oral cancer and the oral cancer exam; these items are not copyrighted and can be reproduced freely. An additional resource is the video posted by the ADA demonstrating the evaluation of a patient for potentially malignant disorders, showing inspection and palpation elements of the intra- and extraoral examination.

The NIDCR52 suggests that a thorough head and neck examination should be a routine part of each patient's dental visit, as follows. Clinicians should be particularly vigilant in checking those who use tobacco or excessive amounts of alcohol.

  • Examine your patients using the head and neck examination protocol described by the NIDCR.
  • Take a history of their alcohol and tobacco use.
  • Inform your patients of the association between tobacco use, alcohol use, and oral cancer.
  • Follow-up to make sure a definitive diagnosis is obtained on any possible signs or symptoms of oral cancer.

A 2019 ADA Policy on “Early Detection and Prevention of Oral and Oropharyngeal Cancer” supports prevention education and routine visual and tactile examinations for all patients.57

Given that mortality rates from OC/OP-SCC have been fairly stable,24 it has been posited that earlier detection of oral cancers will improve prognosis.  A 2015 systematic review and meta-analysis by Seoane et al.58 found that a longer time interval from a patient’s first symptom to referral for diagnosis was a “risk factor for advanced stage and mortality of oral cancer.”

A number of adjuncts to the standard clinical examination have been developed and are intended to improve disease detection. These include oral brush cytology, toluidine blue staining, and light-based detection systems to increase the visibility of oral mucosal lesions or provide real-time data on suspicious mucosal lesions.59 Diagnostic performance in clinical studies has been inconsistent because results vary according to study settings and the sample populations enrolled.59, 60 As noted in the 2017 ADA clinical practice guideline and systematic review,54, 55 it is not yet clear whether these ancillary tests are helpful in triaging which patients need diagnostic or therapeutic follow-up, in part because these tests can also yield false-positive results. Diagnostic adjuncts have been evaluated primarily in referral clinic settings or cancer centers and in patients at high baseline risk of disease.59 Data from studies in general clinic settings and in patients at low baseline risk of disease are more limited, and additional data are needed to characterize test performance in these populations and settings.59

ADA Policy on Early Detection and Prevention of Oral and Oropharyngeal Cancer

EARLY DETECTION AND PREVENTION OF ORAL AND OROPHARYNGEAL CANCER
(Trans.2019:277)

Resolved, that the American Dental Association recognizes that early oral and oropharyngeal cancer diagnosis has the potential to have a significant impact on treatment decisions and outcomes, and supports routine visual and tactile examinations for all patients, and be it further

Resolved, that the Association supports state and local Association-sponsored education activities to promote the prevention and early detection of oral and oropharyngeal cancer.

American Dental Association
Adopted 2019

ADA Policy on HPV Vaccination

HUMAN PAPILLOMAVIRUS (HPV) VACCINATION FOR THE PREVENTION OF INFECTION WITH HPV TYPES ASSOCIATED WITH OROPHARYNGEAL CANCER 
(Trans.2018:351)

Resolved, that the American Dental Association (ADA) adopts the position that HPV vaccination, as recommended by the CDC Advisory Committee on Immunization Practices, is a safe and effective intervention to decrease the burden of oral and oropharyngeal HPV infection; and be it further

Resolved, that the ADA urges dentists, as well as local and state dental societies, to support the use and administration of the HPV vaccine as recommended by the CDC Advisory Committee on Immunization Practices; and

Resolved, that the ADA encourages appropriate external agencies to support research to improve understanding of the natural history of oral HPV infection, transmission risks, screening and testing.

American Dental Association
Adopted 2018

References
  1. National Cancer Institute. Head and neck cancer. National Institutes of Health, 2021. "https://www.cancer.gov/types/head-and-neck/head-neck-fact-sheet". Accessed September 6, 2022.
  2. Chi AC, Day TA, Neville BW. Oral cavity and oropharyngeal squamous cell carcinoma - an update. CA Cancer J Clin 2015;65(5):401-21.
  3. Christopolous C, Moubayed SP, Nader ME, Ayed T, Ghannoum JE. Mouth anatomy: Overview. Medscape. "http://emedicine.medscape.com/article/1899122-overview". Accessed September 13, 2022.
  4. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2022. CA: A Cancer Journal for Clinicians 2022;72(1):7-33.
  5. Howlader N, Noone AM, Krapcho M, et al. SEER cancer statistics review, 1975-2018. Bethesda, MD. "https://seer.cancer.gov/csr/1975_2018/, based on November 2020 SEER data submission, posted to the SEER web site, April 2021".
  6. Stepan KO, Mazul AL, Larson J, et al. Changing epidemiology of oral cavity cancer in the United States. Otolaryngol Head Neck Surg 2022:1945998221098011.
  7. American Cancer Society. Cancer Facts & Figures 2022. Atlanta: American Cancer Society; 2022. "https://www.cancer.org/content/dam/cancer-org/research/cancer-facts-and-statistics/annual-cancer-facts-and-figures/2022/2022-cancer-facts-and-figures.pdf  ". Accessed September 27, 2022.
  8. Hashibe M, Brennan P, Benhamou S, et al. Alcohol drinking in never users of tobacco, cigarette smoking in never drinkers, and the risk of head and neck cancer: Pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. J Natl Cancer Inst 2007;99(10):777-89.
  9. Centers for Disease Control and Prevention (CDC). The health consequences of smoking – 50 years of progress: A report of the surgeon general. Rockville, MD: U.S. Department of Health and Human Services, Office of the Surgeon General 2014. "https://www.ncbi.nlm.nih.gov/books/NBK179276/pdf/Bookshelf_NBK179276.pdf". Accessed September 20, 2022.
  10. Di Credico G, Edefonti V, Polesel J, et al. Joint effects of intensity and duration of cigarette smoking on the risk of head and neck cancer: A bivariate spline model approach. Oral Oncology 2019;94:47-57.
  11. Goldstein BY, Chang SC, Hashibe M, La Vecchia C, Zhang ZF. Alcohol consumption and cancers of the oral cavity and pharynx from 1988 to 2009: An update. Eur J Cancer Prev 2010;19(6):431-65.
  12. Bagnardi V, Rota M, Botteri E, et al. Alcohol consumption and site-specific cancer risk: A comprehensive dose–response meta-analysis. British Journal of Cancer 2015;112(3):580-93.
  13. Di Credico G, Polesel J, Dal Maso L, et al. Alcohol drinking and head and neck cancer risk: The joint effect of intensity and duration. British Journal of Cancer 2020;123(9):1456-63.
  14. Powell SF, Vu L, Spanos WC, Pyeon D. The key differences between human papillomavirus-positive and-negative head and neck cancers: Biological and clinical implications. Cancers 2021;13(20):5206.
  15. Blot WJ, McLaughlin JK, Winn DM, et al. Smoking and drinking in relation to oral and pharyngeal cancer. Cancer Res 1988;48(11):3282-7.
  16. Hashibe M, Brennan P, Chuang SC, et al. Interaction between tobacco and alcohol use and the risk of head and neck cancer: Pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. Cancer Epidemiol Biomarkers Prev 2009;18(2):541-50.
  17. Lingen MW, Xiao W, Schmitt A, et al. Low etiologic fraction for high-risk human papillomavirus in oral cavity squamous cell carcinomas. Oral Oncol 2013;49(1):1-8.
  18. Cleveland JL, Junger ML, Saraiya M, et al. The connection between human papillomavirus and oropharyngeal squamous cell carcinomas in the United States: Implications for dentistry. J Am Dent Assoc 2011;142(8):915-24.
  19. Galati L, Chiocca S, Duca D, et al. HPV and head and neck cancers: Towards early diagnosis and prevention. Tumour Virus Research 2022;14:200245.
  20. Stein AP, Saha S, Kraninger JL, et al. Prevalence of human papillomavirus in oropharyngeal cancer: A systematic review. Cancer J 2015;21(3):138-46.
  21. Liao CI, Francoeur AA, Kapp DS, et al. Trends in human papillomavirus-associated cancers, demographic characteristics, and vaccinations in the US, 2001-2017. JAMA Netw Open 2022;5(3):e222530.
  22. Praud D, Rota M, Rehm J, et al. Cancer incidence and mortality attributable to alcohol consumption. International Journal of Cancer 2016;138(6):1380-87.
  23. Samarasinghe V, Madan V, Lear JT. Management of high-risk squamous cell carcinoma of the skin. Expert Rev Anticancer Ther 2011;11(5):763-9.
  24. Howlader N, Noone AM, Krapcho M, et al. SEER cancer statistics review, 1975-2018, National Cancer Institute. Bethesda, MD.
  25. IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Tobacco smoke and involuntary smoking. IARC Monogr Eval Carcinog Risks Hum 2004;83:1-1438.
  26. Kawakita D, Matsuo K. Alcohol and head and neck cancer. Cancer Metastasis Rev 2017;36(3):425-34.
  27. D’Souza G, Clemens G, Strickler HD, et al. Long-term persistence of oral HPV over 7 years of follow-up. JNCI Cancer Spectrum 2020;4(5).
  28. D'Souza G, McNeel TS, Fakhry C. Understanding personal risk of oropharyngeal cancer: Risk-groups for oncogenic oral HPV infection and oropharyngeal cancer. Ann Oncol 2017;28(12):3065-69.
  29. Drake VE, Fakhry C, Windon MJ, et al. Timing, number, and type of sexual partners associated with risk of oropharyngeal cancer. Cancer 2021;127(7):1029-38.
  30. Jacobs CD, Barbour AB, Mowery YM. The relative distribution of oral cancer in the United States by subsite. Oral Oncology 2019;89:56-58.
  31. Ng JH, Iyer NG, Tan MH, Edgren G. Changing epidemiology of oral squamous cell carcinoma of the tongue: A global study. Head Neck 2017;39(2):297-304.
  32. Patel SC, Carpenter WR, Tyree S, et al. Increasing incidence of oral tongue squamous cell carcinoma in young white women, age 18 to 44 years. J Clin Oncol 2011;29(11):1488-94.
  33. Warnakulasuriya S, Kujan O, Aguirre-Urizar JM, et al. Oral potentially malignant disorders: A consensus report from an international seminar on nomenclature and classification, convened by the WHO collaborating centre for oral cancer. Oral Dis 2021;27(8):1862-80.
  34. Centers for Disease Control and Prevention Human papillomavirus (HPV): HPV and oropharyngeal cancer fact sheet. "https://www.cdc.gov/cancer/hpv/basic_info/hpv_oropharyngeal.htm". Accessed September 14, 2022.
  35. Chaturvedi AK. Epidemiology and clinical aspects of HPV in head and neck cancers. Head Neck Pathol 2012;6 Suppl 1:S16-24.
  36. Pierce Campbell CM, Kreimer AR, Lin H-Y, et al. Long-term persistence of oral human papillomavirus type 16: The HPV infection in men (HIM) study. Cancer prevention research (Philadelphia, Pa.) 2015;8(3):190-96.
  37. Gillison ML, Chaturvedi AK, Anderson WF, Fakhry C. Epidemiology of human papillomavirus-positive head and neck squamous cell carcinoma. J Clin Oncol 2015;33(29):3235-42.
  38. Bragelmann J, Dagogo-Jack I, El Dinali M, et al. Oral cavity tumors in younger patients show a poor prognosis and do not contain viral RNA. Oral Oncol 2013;49(6):525-33.
  39. Sgaramella N, Coates PJ, Strindlund K, et al. Expression of p16 in squamous cell carcinoma of the mobile tongue is independent of HPV infection despite presence of the HPV-receptor syndecan-1. Br J Cancer 2015;113(2):321-6.
  40. Senkomago V, Henley SJ, Thomas CC, et al. Human papillomavirus-attributable cancers - United States, 2012-2016. MMWR Morb Mortal Wkly Rep 2019;68(33):724-28.
  41. Ellington TD, Henley SJ, Senkomago V, et al. Trends in incidence of cancers of the oral cavity and pharynx - United States 2007-2016. MMWR Morb Mortal Wkly Rep 2020;69(15):433-38.
  42. Fakhry C, Fung N, Tewari SR, D'Souza G. Unique role of HPV16 in predicting oropharyngeal cancer risk more than other oncogenic oral HPV infections. Oral Oncol 2020;111:104981.
  43. Human papillomavirus-associated cancers - United States, 2004-2008. MMWR Morb Mortal Wkly Rep 2012;61:258-61.
  44. Osazuwa-Peters N, Simpson MC, Rohde RL, et al. Differences in sociodemographic correlates of human papillomavirus-associated cancer survival in the United States. Cancer Control 2021;28:10732748211041894.
  45. Jordan KH, Fisher JL, Paskett ED. Distinct sociodemographic differences in incidence and survival rates for human papillomavirus (HPV)-like, non-HPV-like, and "other"-like oral cavity and pharynx cancers: An analysis of Surveillance, Epidemiology and End Results (SEER) program data. Front Oncol 2022;12:980900.
  46. Mahal BA, Catalano PJ, Haddad RI, et al. Incidence and demographic burden of HPV-associated oropharyngeal head and neck cancers in the United States. Cancer Epidemiology, Biomarkers & Prevention 2019;28(10):1660-67.
  47. Windon MJ, D'Souza G, Rettig EM, et al. Increasing prevalence of human papillomavirus-positive oropharyngeal cancers among older adults. Cancer 2018;124(14):2993-99.
  48. Chaturvedi AK, Graubard BI, Broutian T, et al. Effect of prophylactic human papillomavirus (HPV) vaccination on oral HPV infections among young adults in the United States. J Clin Oncol 2018;36(3):262-67.
  49. American Academy of Pediatric Dentistry. Policy on human papilloma virus vaccinations.  2020. "https://www.aapd.org/media/Policies_Guidelines/P_HPV_Vaccinations.pdf". Accessed September 14, 2022.
  50. U.S. Food and Drug Administration FDA news release: FDA approves expanded use of Gardasil 9 to include individuals 27 through 45 years old.  2018. "https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm622715.htm". Accessed September 14, 2022.
  51. Villa A, Patton LL, Giuliano AR, et al. Summary of the evidence on the safety, efficacy, and effectiveness of human papillomavirus vaccines: Umbrella review of systematic reviews. J Am Dent Assoc 2020;151(4):245-54.e24.
  52. National Institute of Dental and Craniofacial Research. Detecting oral cancer: A guide for health care professionals. National Institutes of Health July 2013. "https://www.nidcr.nih.gov/sites/default/files/2017-09/detecting-oral-cancer-poster.pdf". Accessed September 14, 2022.
  53. Kreimer AR, Chaturvedi AK, Alemany L, et al. Summary from an international cancer seminar focused on human papillomavirus (HPV)-positive oropharynx cancer, convened by scientists at IARC and NCI. Oral Oncol 2020;108:104736.
  54. Lingen MW, Abt E, Agrawal N, et al. Evidence-based clinical practice guideline for the evaluation of potentially malignant disorders in the oral cavity: A report of the American Dental Association. J Am Dent Assoc 2017;148(10):712-27.e10.
  55. Lingen MW, Tampi MP, Urquhart O, et al. Adjuncts for the evaluation of potentially malignant disorders in the oral cavity: Diagnostic test accuracy systematic review and meta-analysis-a report of the American Dental Association. J Am Dent Assoc 2017;148(11):797-813.e52.
  56. U.S. Preventive Services Task Force. Final recommendation statement: Oral cancer: Screening.  2013. "http://www.uspreventiveservicestaskforce.org/Page/Document/RecommendationStatementFinal/oral-cancer-screening1". Accessed September 14, 2022.
  57. American Dental Association. Current Policies adopted 1954–2016: Early detection and prevention of oral and oropharyngeal cancer (Trans.2019:277).  2019. "http://www.ada.org/en/member-center/leadership-governance//-/media/project/ada-organization/ada/ada-org/files/advocacy/current_policies.pdf". Accessed September 14, 2022.
  58. Seoane J, Alvarez-Novoa P, Gomez I, et al. Early oral cancer diagnosis: The Aarhus statement perspective. A systematic review and meta-analysis. Head Neck 2015.
  59. Cankaya H, Guneri P, Epstein JB. Adjunctive methods and devices for clinical detection of oral squamous cell carcinoma. Oral Health Prev Dent 2015;13(1):29-39.
  60. Walsh T, Macey R, Kerr AR, et al. Diagnostic tests for oral cancer and potentially malignant disorders in patients presenting with clinically evident lesions. Cochrane Database Syst Rev 2021;7(7):Cd010276.
ADA Resources
Reviewed by: Clinical Excellence Subcommittee, ADA Council on Scientific Affairs
Topic Last Updated: September 30, 2022

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Research Services and Scientific Information, ADA Library & Archives.