Skip to main content
Journal of the Advanced Practitioner in Oncology logoLink to Journal of the Advanced Practitioner in Oncology
. 2015 May 1;6(3):256–262. doi: 10.6004/jadpro.2015.6.3.7

Significance of Human Papillomavirus in Head and Neck Cancers

Kristy Lynn Boggs 1
PMCID: PMC4625631  PMID: 26557412

Over 45,000 Americans are estimated to be newly diagnosed with cancer of the oral cavity and pharynx in 2015, and an estimated 8,650 will die of the disease (Siegel, Miller, & Jemal, 2015). It is well known that the combination of smoking and alcohol use increases the risk for developing head and neck squamous cell carcinoma (HNSCC). Head and neck squamous cell carcinoma is a general term that encompasses cancers of the nasal cavity, sinuses, lips, mouth, salivary glands, throat, and larynx. HNSCC has been considered to be a cancer predominantly seen in men of older age (National Cancer Institute [NCI], 2013).

The current trends, deaths, and survival rates demonstrate a modest decrease in HNSCC from 1975 to 2006 (NCI, 2015). However, despite this general decrease, research demonstrates that oropharyngeal-specific cancers are rising (American Cancer Society, 2015; Gillison et al., 2012).

Currently, there is evidence that tissue collected from patients diagnosed with head and neck cancer may be positive for human papillomavirus (HPV) DNA, particularly cancers of the oropharyngeal site (Mehanna et al., 2013). The oropharynx refers to the middle part of the throat behind the mouth, including the back third of the tongue, the soft palate, the side and back walls of the throat, and the tonsils (NCI, 2015).

According to the Centers for Disease Control and Prevention (CDC, 2013), 79 million people have HPV, and over 14 million cases are newly diagnosed each year. This virus is associated with cancer of the cervix, vagina, penis, and anus. The exact incidence of HPV-positive HNSCC is unknown and could be largely misrepresented because current practice does not support testing all HNSCC for HPV status.

Currently, the Surveillance, Epidemiology, and End Results Program (SEER) does not specify HPV status in statistics on oral cavity and pharynx cancers. However, according to the CDC (2014a), an estimated 72% of oropharyngeal cancers may be attributed to HPV infections, with more than 2,370 new cases diagnosed in women and nearly 9,356 new cases diagnosed in men every year in the United States.

PATHOPHYSIOLOGY

Over 100 different subtypes of HPV have been discovered (CDC, 2012). Most subtypes cause common skin warts. These types are categorized as low or high risk. Low-risk types, such as HPV-6 and HPV-11, can cause benign papillomas (commonly called warts). Generally, infections with these types tend to resolve themselves spontaneously within 12 months.

However, high-risk types such as HPV-16 and HPV-18 can lead to chronic infection, cellular abnormalities, and then cancer. HPV-16 is linked to HNSCC of the oropharynx (American Cancer Society, 2015). Approximately 90% of HPV-related oropharyngeal cancers are positive for the HPV-16 subtype (Blitzer, Smith, Harris, & Kimple, 2014; D’Souza, Cullen, Bowie, Thorpe, & Fakhry, 2014; Gan, Zhang, Guo, & Fan, 2014; Gillison et al., 2012). Commons symptoms may vary and can be vague (NCI, 2015; see Table).

Table 1.

Table 1

Signs and Symptoms of Oropharyngeal Cancer

Infection with high-risk types of HPV can cause cells to make two proteins: E6 and E7. These proteins can turn off certain genes that control cell proliferation. Uncontrolled cell proliferation or cell growth can lead to cancer (American Cancer Society, 2015; Blitzer et al., 2014; see Figure 1).

Figure 1.

Figure 1

Mechanism of HPV-16 and tumorigenesis. HPV-16 = human papillomavirus subtype 1; pRB = protein retinoblastoma.

RISK FACTORS

Sexual Behavior

Human papillomavirus infection can spread from one person to another through sexual contact, including vaginal, anal, and oral sex. Oral sexual behavior and open-mouth kissing have been linked to an increased risk for oropharyngeal infection ( D’Souza., 2014; Geiger et al., 2014). In addition, similar to cervical cancer in women, the number of sexual partners can increase the risk for an HPV-positive tumor of the head and neck (American Cancer Society, 2015; CDC, 2013; D’Souza., 2014; Geiger et al., 2014; Gillison et al., 2012; Kero et al., 2014a).

Current data indicate that oropharyngeal cancer is more prevalent in men than in women (CDC, 2013). D’Souza et al. (2014) found that sexual behavior alone accounted for these differences, with men tending to have more lifetime sexual partners than women. However, Gillison et al. (2012) demonstrated that after adjusting for high-risk sexual behavior, men continued to be at higher risk than women. To date, no strong evidence exists to explain why men are more affected by HPV-positive oropharyngeal cancers than women (Giuliano et al., 2014). The variation in prevalence surrounding gender and anatomic sites affected deserves further investigation.

Smoking

Smoking is a known carcinogenic that can cause changes in the DNA of cells and contribute to the increased risk for many types of cancers. Several studies demonstrate that smoking status can contribute to the persistence of HPV infection (Daling et al., 2004; Haukioja, Asunta, Söderling, & Syrjänen, 2014; Kero et al., 2014b). Smoking is considered an independent risk factor for HPV infection (Gillison et al., 2012).

Precisely how smoking contributes to chronic HPV infection and its progression to malignancy remains elusive. Castle (2008) discussed some plausible theories. First, smoking decreases immunity, which can reduce the body’s ability to effectively clear HPV infection. This, in turn, causes chronic infection and inflammation. Second, infection with high-risk HPV subtypes can cause uncontrolled cellular proliferation. These molecular changes combined with the carcinogens in tobacco smoke can work synergistically to encourage cancer development.

In addition, studies have indicated that smoking can adversely affect response to treatment and prognosis (Haughey & Sinha, 2012; Jensen, Jensen, & Grau, 2007; Moreira et al., 2014; Olthof et al., 2015). A review of the literature by Sobus and Warren (2014) revealed that smoking encourages further proliferation, metastasis, angiogenesis, and reduced apoptosis in cancer cells. This process can cause poor treatment response, increased recurrence of primary tumors, and increased mortality.

Oral Hygiene

There may be an association with poor oral hygiene that leads to an increased risk of developing HPV-positive HNSCC (Bui, Markham, Ross, & Mullen, 2013; Tezal et al., 2012). Poor oral hygiene leads to the accumulation of bacteria and microorganisms in the mouth, causing chronic inflammation, mucosal damage, and some microulceration.

Chronic inflammation plays several key roles in the development of cancer. According to Bonomi et al. (2014), chronic inflammation causes specific substances normally released during inflammation to facilitate healing to be constantly activated. These substances can then aid in tumor progression through increased proliferation, angiogenesis, and carcinogenesis. In addition, inflammation causes hypoxia to tissues resulting in DNA damage, leading to gene mutations that promote tumorigenesis.

MANAGEMENT

In 2014, the National Comprehensive Cancer Network (NCCN) recommendations included testing tumors for HPV in the initial workup of oropharyngeal cancers (NCCN, 2014). Recommendations include either an immunohistochemistry for analysis of p16 expression or HPV in situ hybridization for detection of HPV DNA in tumor cell nuclei (NCCN, 2014). Testing is not considered in management decisions, however, and is used for prognosis purposes.

Current treatment guidelines, depending on stage, consist mainly of surgery, radiation therapy, chemoradiation therapy, and targeted therapies (National Cancer Institute, 2015). In a majority of studies, HPV-positive patients showed better prognosis and 5-year survival than HPV-negative patients with HNSCC (Ang & Sturgis, 2012; Chaturvedi, Engels, Anderson, & Gillison, 2008; Dufour, Beby-Defaux, Agius, & Lacau St. Guily, 2012; Fakhry et al., 2008; Ljokjel et al., 2014; Mirghani et al., 2014). It is speculated that the current guidelines for treatment could be minimized, given the more favorable prognosis of HPV-positive cancers, which subsequently could minimize side effects without affecting prognosis (Geiger et al., 2014; Masterson et al., 2014). However, there is currently insufficient evidence to change treatment guidelines based on HPV status in HNSCC (Masterson et al., 2014; Mehanna, Olaleye, & Licitra, 2012).

Vaccines

There are currently two HPV vaccines approved by the US Food and Drug Administration (FDA): Gardasil and Cervarix. Gardasil is quadrivalent and protects against HPV subtypes 6, 11, 16, and 18. Subtypes 6 and 11 are associated with genital warts. Cervarix is bivalent and protects against oncogenic types 16 and 18. These vaccines are currently approved to prevent cervical cancer and precancers in women.

The FDA has approved both vaccines to be given to girls between the ages of 9 and 26 and has currently approved Gardasil for boys between the ages of 9 and 21 to prevent genital warts. For women older than 26 and men older than 21 who did not receive the vaccine or did not receive all three doses, the vaccine can still be given. The CDC currently recommends that girls receive three doses of either vaccine at the age of 11 or 12. The future impact these vaccines may have on the prevalence of HPV-positive tumors of the head and neck is thus far undetermined.

Psychosocial Impact

Human papillomavirus has only newly been associated with cancers of the head and neck. The impact of discussing HPV results with patients and their partners has not been well studied (Baxi et al., 2013). Current research or information regarding strategies for discussion is minimal, thus there are currently no established guidelines for discussing HPV as it relates to oropharyngeal cancer. However, numerous studies have demonstrated that many women diagnosed with high-risk HPV-positive cervical cancers have experienced considerable psychological stress related to their diagnosis. Similar distress was discovered in men being tested and diagnosed with HPV-positive HNSCC (Cook, 2014; Daley et al., 2012; Harvey-Knowles & Kosenko, 2012).

Patients newly diagnosed with HPV-positive HNSCC can experience misconceptions and uncertainty regarding its transmission, latency, and future spread (Baxi et al., 2013). In a report examining the cognitive and emotional responses associated with HPV test results, the men who tested positive experienced negative emotional responses and were less likely to disclose the diagnosis with current or future partners (Daley et al., 2012). Furthermore, an exploratory study revealed that most patients lacked the knowledge connecting HPV status to their current cancer diagnosis and expressed interest in additional education (Milbury, Rosenthal, El-Naggar, & Badr, 2013). A systematic review regarding appropriate counseling messages for patients with HPV and associated conditions provided suggestions for clinical providers to lead such a discussion (Dunne, Friedman, Datta, Markowitz, & Workowski, 2011).

There are some commonalities between these suggestions and the CDC’s current key messages for women receiving cervical cancer screening and HPV testing (2011). For instance, it is important to deliver information in both verbal and written formats within a neutral, nonstigmatizing context. Teaching should focus on prevalence, signs and symptoms, and risk to partners. To reduce possible accusations between couples, providers must emphasize that HPV can remain dormant for many years and that having HPV does not imply infidelity, nor should it necessarily raise concerns about a partner’s health (CDC, 2011). It is reasonable to consider that similar topics will be useful in patients newly diagnosed with HPV-positive HNSCC. All clinical providers should aim to decrease any feelings of stigmatism or guilt that patients frequently experience with the diagnosis of a sexually transmitted infection (STI).

Moreover, what makes this even more challenging for these patients is being told that not only do they have cancer but that it may be related to an STI they contracted. This can add additional distress and confusion. Some possible strategies and key messages to convey to patients might include the prevalence of HPV, its transmission and prognosis, partner risk, and limitations in our present knowledge (Evans & Powell, 2014; Fakhry et al., 2008; Geiger et al., 2014; Kosenko, Craig, & Harvey-Knowles, 2012; see Figure 2).

Figure 2.

Figure 2

Suggested discussion points for having conversations with patients about the human papillomavirus. HPV = human papillomavirus; CDC = Centers for Disease Control and Prevention; HNSCC = head and neck squamous cell carcinoma

CONSIDERATIONS FOR THE ADVANCED PRACTITIONER

Currently, there are apparent gaps in knowledge regarding HPV-positive HNSCC. As research continues to expand, our understanding of the impact of these types of cancers will continue to change and develop. Discussion regarding the significance of an HPV-positive cancer can be complex and confusing. Future studies can help to guide advanced practitioners (APs) to identify key messages pertinent to patients and the most effective approaches to successful communication. It is imperative that the AP understand the impact of HPV on cancer development in all areas of medicine. Understanding the impact of HPV-related cancers and associated risk factors should guide the physical exam and informative discussions during patient visits. Identifying risk factors can aid in prevention and early detection in the general public. Educating the public and patients regarding risk factors for HPV can help reduce infection rates and thus prevent cancer from developing.

The oncology AP, in particular, may be the initial provider to inform patients about HPV testing, diagnosis, and prognosis as it relates to their cancer. It is important that these providers appreciate the common challenges and concerns patients may experience to enhance effective communication, reduce misconceptions, and ensure compliance with treatment.

Thus, it is essential for the AP to keep up with the developments in HPV diagnosis as they relate to specific cancers. The AP is in the unique position of having the ability to care for and foster trusting relationships with their patients and their families, as well as possessing advanced knowledge in medical practice. Consequently, the AP is the most appropriate provider to lead the way for future research exploring the psychological impact in the diagnosis of HPV-positive HNSCC.

Footnotes

The author has no potential conflicts of interest to disclose.

References

  • 1.Oral cavity and oropharyngeal cancer. American Cancer Society. 2015 Retrieved from http://www.cancer.org/cancer/oralcavityandoropharyngealcancer/detailedguide/oral-cavity-and-oropharyngeal-cancer-key-statistics.
  • 2.Ang Kie Kian, Sturgis Erich M. Human papillomavirus as a marker of the natural history and response to therapy of head and neck squamous cell carcinoma. Seminars in radiation oncology. 2012;22:128–142. doi: 10.1016/j.semradonc.2011.12.004. [DOI] [PubMed] [Google Scholar]
  • 3.Baxi Shrujal S, Shuman Andrew G, Corner Geoffrey W, Shuk Elyse, Sherman Eric J, Elkin Elena B, Hay Jennifer L, Pfister David G. Sharing a diagnosis of HPV-related head and neck cancer: the emotions, the confusion, and what patients want to know. Head & neck. 2013;35:1534–1541. doi: 10.1002/hed.23182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Blitzer Grace C, Smith Molly A, Harris Stephen L, Kimple Randall J. Review of the clinical and biologic aspects of human papillomavirus-positive squamous cell carcinomas of the head and neck. International journal of radiation oncology, biology, physics. 2014;88:761–770. doi: 10.1016/j.ijrobp.2013.08.029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Bonomi Marcelo, Patsias Alexis, Posner Marshall, Sikora Andrew. The role of inflammation in head and neck cancer. Advances in experimental medicine and biology. 2014;816:107–127. doi: 10.1007/978-3-0348-0837-8_5. [DOI] [PubMed] [Google Scholar]
  • 6.Bui Thanh Cong, Markham Christine M, Ross Michael Wallis, Mullen Patricia Dolan. Examining the association between oral health and oral HPV infection. Cancer prevention research (Philadelphia, Pa.) 2013;6:917–924. doi: 10.1158/1940-6207.CAPR-13-0081. [DOI] [PubMed] [Google Scholar]
  • 7.Castle P. E. How does tobacco smoke contribute to cervical carcinogenesis? Journal of Virology. 2008;82:6084–6086. doi: 10.1128/JVI.00103-08. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.HPV-associated oropharyngeal cancer rates by race and ethnicity. Centers for Disease Control and Prevention. 2014a Retrieved from http://www.cdc.gov/cancer/hpv/statistics/headneck.htm.
  • 9.HPV-associated oropharyngeal cancer rates by race and ethnicity. Centers for Disease Control and Prevention. 2014a Retrieved from http://www.cdc.gov/cancer/hpv/statistics/headneck.htm.
  • 10.Cervical cancer screening for women who attend STD clinics or have a history of STDs. Centers for Disease Control and Prevention. 2014b Retrieved from http://www.cdc.gov/std/treatment/2010/cc-screening.htm.
  • 11.Chaturvedi Anil K, Engels Eric A, Anderson William F, Gillison Maura L. Incidence trends for human papillomavirus-related and -unrelated oral squamous cell carcinomas in the United States. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2008;26:612–619. doi: 10.1200/JCO.2007.14.1713. [DOI] [PubMed] [Google Scholar]
  • 12.Cook Catherine. The sexual health consultation as a moral occasion. Nursing inquiry. 2014;21:11–19. doi: 10.1111/nin.12018. [DOI] [PubMed] [Google Scholar]
  • 13.D’Souza G., Cullen K., Bowie J., Thorpe R., Fakhry C. Differences in oral sexual behaviors by gender, age, and race explain observed differences in prevalence of oral human papillomavirus infection. PLoS One. 2014;9:e86023. doi: 10.1371/journal.pone.0086023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Daley Ellen M, Buhi Eric R, Marhefka Stephanie L, Baker Elizabeth A, Kolar Stephanie, Ebbert-Syfrett Judith, Vamos Cheryl A, Abrahamsen Martha, Giuliano Anna R. Cognitive and emotional responses to human papillomavirus test results in men. American journal of health behavior. 2012;36:770–785. doi: 10.5993/AJHB.36.6.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Daling Janet R, Madeleine Margaret M, Johnson Lisa Godefroy, Schwartz Stephen M, Shera Katherine A, Wurscher Michelle A, Carter Joseph J, Porter Peggy L, Galloway Denise A, McDougall James K. Human papillomavirus, smoking, and sexual practices in the etiology of anal cancer. Cancer. 2004;101:270–280. doi: 10.1002/cncr.20365. [DOI] [PubMed] [Google Scholar]
  • 16.Dufour X, Beby-Defaux A, Agius G, Lacau St Guily J. HPV and head and neck cancer. European annals of otorhinolaryngology, head and neck diseases. 2012;129:26–31. doi: 10.1016/j.anorl.2011.05.004. [DOI] [PubMed] [Google Scholar]
  • 17.Dunne Eileen F, Friedman Allison, Datta S Deblina, Markowitz Lauri E, Workowski Kimberly A. Updates on human papillomavirus and genital warts and counseling messages from the 2010 Sexually Transmitted Diseases Treatment Guidelines. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2011;53 Suppl 3:S143–152. doi: 10.1093/cid/cir703. [DOI] [PubMed] [Google Scholar]
  • 18.Evans Mererid, Powell Ned G. Sexual health in oral oncology: breaking the news to patients with human papillomavirus-positive oropharyngeal cancer. Head & neck. 2014;36:1529–1533. doi: 10.1002/hed.23792. [DOI] [PubMed] [Google Scholar]
  • 19.Fakhry Carole, Westra William H, Li Sigui, Cmelak Anthony, Ridge John A, Pinto Harlan, Forastiere Arlene, Gillison Maura L. Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trial. Journal of the National Cancer Institute. 2008;100:261–269. doi: 10.1093/jnci/djn011. [DOI] [PubMed] [Google Scholar]
  • 20.Gan Li-Li, Zhang Hao, Guo Ji-Hua, Fan Ming-Wen. Prevalence of human papillomavirus infection in oral squamous cell carcinoma: a case-control study in Wuhan, China. Asian Pacific journal of cancer prevention : APJCP. 2014;15:5861–5865. doi: 10.7314/apjcp.2014.15.14.5861. [DOI] [PubMed] [Google Scholar]
  • 21.Geiger Jessica L, Lazim Ahmed F, Walsh Francis J, Foote Robert L, Moore Eric J, Okuno Scott H, Olsen Kerry D, Kasperbauer Jan L, Price Daniel L, Garces Yolanda I, Ma Daniel J, Neben-Wittich Michelle A, Molina Julian R, Garcia Joaquin J, Price Katharine A R. Adjuvant chemoradiation therapy with high-dose versus weekly cisplatin for resected, locally-advanced HPV/p16-positive and negative head and neck squamous cell carcinoma. Oral oncology. 2014;50:311–318. doi: 10.1016/j.oraloncology.2014.01.001. [DOI] [PubMed] [Google Scholar]
  • 22.Gillison Maura L, Broutian Tatevik, Pickard Robert K L, Tong Zhen-you, Xiao Weihong, Kahle Lisa, Graubard Barry I, Chaturvedi Anil K. Prevalence of oral HPV infection in the United States, 2009-2010. JAMA. 2012;307:693–703. doi: 10.1001/jama.2012.101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Giuliano Anna R, Nyitray Alan G, Kreimer Aimée R, Pierce Campbell Christine M, Goodman Marc T, Sudenga Staci L, Monsonego Joseph, Franceschi Silvia. EUROGIN 2014 roadmap: differences in human papillomavirus infection natural history, transmission and human papillomavirus-related cancer incidence by gender and anatomic site of infection. International journal of cancer. Journal international du cancer. 2015;136:2752–2760. doi: 10.1002/ijc.29082. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Harvey-Knowles Jacquelyn A, Kosenko Kami A. Diagnosing women with HPV: the impact of diagnosis disclosure methods. Patient education and counseling. 2012;88:152–156. doi: 10.1016/j.pec.2012.02.002. [DOI] [PubMed] [Google Scholar]
  • 25.Haughey Bruce H, Sinha Parul. Prognostic factors and survival unique to surgically treated p16+ oropharyngeal cancer. The Laryngoscope. 2012;122 Suppl 2:S13–33. doi: 10.1002/lary.23493. [DOI] [PubMed] [Google Scholar]
  • 26.Haukioja Anna, Asunta Maribel, Söderling Eva, Syrjänen Stina. Persistent oral human papillomavirus infection is associated with smoking and elevated salivary immunoglobulin G concentration. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 2014;61:101–106. doi: 10.1016/j.jcv.2014.06.012. [DOI] [PubMed] [Google Scholar]
  • 27.Jensen Kenneth, Jensen Anders Bonde, Grau Cai. Smoking has a negative impact upon health related quality of life after treatment for head and neck cancer. Oral oncology. 2007;43:187–192. doi: 10.1016/j.oraloncology.2006.02.006. [DOI] [PubMed] [Google Scholar]
  • 28.Kero K M, Rautava J, Syrjänen K, Kortekangas-Savolainen O, Grenman S, Syrjänen S. Stable marital relationship protects men from oral and genital HPV infections. European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology. 2014;33:1211–1221. doi: 10.1007/s10096-014-2061-7. [DOI] [PubMed] [Google Scholar]
  • 29.Kero K, Rautava J, Syrjänen K, Willberg J, Grenman S, Syrjänen S. Smoking increases oral HPV persistence among men: 7-year follow-up study. European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology. 2014;33:123–133. doi: 10.1007/s10096-013-1938-1. [DOI] [PubMed] [Google Scholar]
  • 30.Kosenko Kami A, Craig Elizabeth, Harvey-Knowles Jacquelyn. Helpful and challenging support encounters in the aftermath of HPV infection and diagnosis. Issues in mental health nursing. 2012;33:355–362. doi: 10.3109/01612840.2012.671440. [DOI] [PubMed] [Google Scholar]
  • 31.Ljøkjel Borghild, Lybak Stein, Haave Hilde, Olofsson Jan, Vintermyr Olav K, Aarstad Hans Jørgen. The impact of HPV infection on survival in a geographically defined cohort of oropharynx squamous cell carcinoma (OPSCC) patients in whom surgical treatment has been one main treatment. Acta oto-laryngologica. 2014;134:636–645. doi: 10.3109/00016489.2014.886336. [DOI] [PubMed] [Google Scholar]
  • 32.Masterson L., Moualed D., Masood A., Dwivedi R. C., Benson R., Sterling J. C., Goon P. De-escalation treatment protocols for human papillomavirus-associated oropharyngeal squamous cell carcinoma. Cochrane Database of Systematic Reviews. 2014;2:CD010271. doi: 10.1002/14651858.CD010271.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Mehanna Hisham, Beech Tom, Nicholson Tom, El-Hariry Iman, McConkey Christopher, Paleri Vinidh, Roberts Sally. Prevalence of human papillomavirus in oropharyngeal and nonoropharyngeal head and neck cancer--systematic review and meta-analysis of trends by time and region. Head & neck. 2013;35:747–755. doi: 10.1002/hed.22015. [DOI] [PubMed] [Google Scholar]
  • 34.Mehanna Hisham, Olaleye Oladejo, Licitra Lisa. Oropharyngeal cancer - is it time to change management according to human papilloma virus status? Current opinion in otolaryngology & head and neck surgery. 2012;20:120–124. doi: 10.1097/MOO.0b013e3283509735. [DOI] [PubMed] [Google Scholar]
  • 35.Milbury Kathrin, Rosenthal David I, El-Naggar Adel, Badr Hoda. An exploratory study of the informational and psychosocial needs of patients with human papillomavirus-associated oropharyngeal cancer. Oral oncology. 2013;49:1067–1071. doi: 10.1016/j.oraloncology.2013.07.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Mirghani Haitham, Ugolin Nicolas, Ory Catherine, Lefèvre Marine, Baulande Sylvain, Hofman Paul, St Guily Jean Lacau, Chevillard Sylvie, Lacave Roger. A predictive transcriptomic signature of oropharyngeal cancer according to HPV16 status exclusively. Oral oncology. 2014;50:1025–1034. doi: 10.1016/j.oraloncology.2014.07.019. [DOI] [PubMed] [Google Scholar]
  • 37.Moreira Daniel M, Aronson William J, Terris Martha K, Kane Christopher J, Amling Christopher L, Cooperberg Matthew R, Boffetta Paolo, Freedland Stephen J. Cigarette smoking is associated with an increased risk of biochemical disease recurrence, metastasis, castration-resistant prostate cancer, and mortality after radical prostatectomy: results from the SEARCH database. Cancer. 2014;120:197–204. doi: 10.1002/cncr.28423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Head and neck cancers. National Cancer Institute. 2013 Retrieved from http://www.cancer.gov/cancertopics/types/head-and-neck/head-neck-fact-sheet.
  • 39.Cancer of the oral cavity and pharynx. National Cancer Institute. 2015 Retrieved from http://seer.cancer.gov/statfacts/html/oralcav.html.
  • 40.NCCN Clinical Practice Guidelines in Oncology: Head and neck cancers. National Comprehensive Cancer Network. 2014 doi: 10.6004/jnccn.2020.0031. Retrieved from http://www.nccn.org/professionals/physician_gls/pdf/head-and-neck.pdf. [DOI] [PubMed]
  • 41.Olthof Nadine C, Huebbers Christian U, Kolligs Jutta, Henfling Mieke, Ramaekers Frans C S, Cornet Iris, van Lent-Albrechts Josefa A, Stegmann Alexander P A, Silling Steffi, Wieland Ulrike, Carey Thomas E, Walline Heather M, Gollin Susanne M, Hoffmann Thomas K, de Winter Johan, Kremer Bernd, Klussmann Jens P, Speel Ernst-Jan M. Viral load, gene expression and mapping of viral integration sites in HPV16-associated HNSCC cell lines. International journal of cancer. Journal international du cancer. 2015;136:E207–218. doi: 10.1002/ijc.29112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Siegel R. L., Miller K. D., Jemal A. Cancer statistics, 2015. CA. A Cancer Journal for Clinicians. 2015;65:5–29. doi: 10.3322/caac.21254. [DOI] [PubMed] [Google Scholar]
  • 43.Sobus Samantha L, Warren Graham W. The biologic effects of cigarette smoke on cancer cells. Cancer. 2014;120:3617–3626. doi: 10.1002/cncr.28904. [DOI] [PubMed] [Google Scholar]
  • 44.Tezal Mine, Scannapieco Frank A, Wactawski-Wende Jean, Hyland Andrew, Marshall James R, Rigual Nestor R, Stoler Daniel L. Local inflammation and human papillomavirus status of head and neck cancers. Archives of otolaryngology--head & neck surgery. 2012;138:669–675. doi: 10.1001/archoto.2012.873. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of the Advanced Practitioner in Oncology are provided here courtesy of BroadcastMed LLC

RESOURCES