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. Author manuscript; available in PMC: 2014 Dec 12.
Published in final edited form as: Oral Oncol. 2013 Jul 19;49(9):863–871. doi: 10.1016/j.oraloncology.2013.06.002

Discussing the diagnosis of HPV-OSCC: common questions and answers

Carole Fakhry 1, Gypsyamber D’Souza 2
PMCID: PMC4264664  NIHMSID: NIHMS647259  PMID: 23876627

Abstract

Human papillomavirus (HPV) is responsible for a rising proportion of oropharyngeal squamous cell cancers (OSCC). HPV-positive OSCCs (HPV-OSCC) are associated with oral HPV infection and sexual behavior. Patient questions regarding risk factors, prognosis and implications for past, present and future relationships often arise. This manuscript addresses frequently asked questions by patients with HPV-OSCC and their families. A framework for clinicians to address these conversations and the limitations of our present knowledge base is also presented.

HPV and its role in OSCC

Human papillomavirus (HPV), a sexually transmitted infection, is now responsible for the overwhelming majority of oropharyngeal squamous cell cancers (OSCC) in the United States (U.S.). Historically, tobacco and alcohol use accounted for the majority of head and neck cancers. However, with the decline of tobacco use in the U.S., the incidence of smoking-related (HPV-negative) oropharyngeal malignancies has decreased.1 The proportion of oropharyngeal cancers attributable to HPV (HPV-positive OSCC; HPV-OSCC) has risen substantially in the U.S. Indeed, while only 16% of OSCCs in the 1980s were HPV-positive, approximately 73% of tumors in the 2000s were HPV-positive. Not only is the proportion of OSCCs that are HPV-positive rising, but the incidence of OSCC is also rising. From 1988 to 2004, there was a 28% increase in incidence of OSCC in the U.S., which was primarily among younger men, ages 50–59.1 Currently, the incidence of OSCC in the U.S. is 6.2 per 100,000, and 1.4 per 100,000 among men and women, respectively.2 There is also data emerging that HPV is etiologically associated with a smaller subset of oral cavity tumors.3

HPV-OSCC has been recognized in the past 10 years as a distinct disease entity. These cancers are associated with oral HPV infection and sexual behavior (a surrogate for oral HPV exposure), although HPV-OSCC is diagnosed in many people who have a modest number of lifetime sexual partners. Individuals with HPV-OSCC, when compared to those with HPV-negative tumors, tend to be white, male, non-smokers and non-drinkers.4 Patients with HPV-OSCC have significantly better prognosis than those with HPV-negative OSCC.5, 6 Given its prognostic significance, HPV tumor detection has been integrated into National Comprehensive Cancer Network (NCCN) guidelines in the diagnostic evaluation of patients with OSCC, thus establishing HPV detection as a clinical standard of care for oropharyngeal malignancy.7

Nuances in discussing the diagnosis of HPV-OSCC with patients

Despite the recognition of HPV-OSCC “epidemic” among head and neck oncology, the impact of providing an HPV-related diagnosis to OSCC patients has not been studied to date. This diagnosis is complex and multi-faceted. The diagnosis of HPV-OSCC imparts upon a patient a cancer diagnosis coupled with the diagnosis of a sexually transmitted infection (STI). The former part of the diagnosis is similar to diagnoses the oncologic team routinely provides and has been trained to discuss. However, the etiologic association of STI and cancer is one that has emerged on the doorstep of the head and neck care team in the last decade, without education regarding the psychosocial ramifications of STI diagnoses. As opposed to gynecologic-oncologists, for instance, who discuss cervical cancer with patients routinely and are trained in diagnosing and treating STIs (cervical dysplasia, Chlamydia, etc.) head and neck surgical, radiation, and medical oncologists currently have no training in discussing STIs. Yet, the head and neck team is now in a position to not only discuss the etiology of a STI-related malignancy, but to counsel their patients and partners regarding complex social and behavioral questions outside the realm of oncology, as patients and partners wrestle with the knowledge that the malignancy was caused by a STI.

Clinically, the multidisciplinary head and neck cancer team is reasonably equipped to counsel patients on the link between tobacco, alcohol and cancer, as well as tobacco and alcohol cessation, although studies show low physician compliance and low levels of confidence to counsel patients.811 The psychosocial distress of a cancer diagnosis has long been recognized, especially in the head and neck patient population.12 By contrast, there is a paucity of head and neck literature regarding counseling of patients with a diagnosis of a STI- related cancer. Therefore, this manuscript is intended to address concerns of patients with HPV-OSCC and their families, and the behavioral questions that frequently arise among practitioners diagnosing, treating, and following this unique patient population.

Few resources currently exist to answer HPV-OSCC patients’ behavioral questions about how, when, and why they got this cancer. The answers to these questions have implications for past, present, and future relationships and must therefore be carefully considered before providing advice to patients. Because these issues have not been well explored in an evidence-based method, it is important in discussions with patients to contextualize many of these answers with “we do not know, however, initial evidence suggests that…” Therefore, we present our best answers to these difficult questions with the caveat that in many cases, the answers to these questions are not yet established and can currently only be extrapolated from related research on anogenital HPV infection, initial oral HPV literature, and an understanding of the distinctions between oral and cervical HPV infection.

This manuscript addresses common patient concerns related to behaviors associated with HPV-OSCC and oral HPV infection, and reviews what is currently known and what remains unknown about oral HPV acquisition and transmission. A patient brochure with commonly asked questions and answers is also included (Figure 1), which providers may give to their patients to supplement and reinforce their counseling regarding HPV-OSCC.

Figure 1.

Figure 1

Figure 1

Discussing tumor HPV status in OSCC

Despite inclusion of HPV detection in NCCN guidelines for cancers of the oropharynx, there are no formal recommendations at present for when and how to discuss HPV test results with patients. Given that cervical HPV and cervical cancer literature has been used as the paradigm for oral HPV and HPV-OSCC research, until a similar body of literature is generated for HPV-OSCC, we can use the cervical HPV counseling messages created by CDC as a starting point.

The cervical HPV counseling guidelines generated by the CDC suggest that physicians discuss the significance of cervical HPV infection and reasons for the test before performing the test.13 In addition to the verbal conversation, the guidelines recommend that physicians provide patients with documentation in layman’s terms to summarize HPV and how it is associated with cervical cancer.13 When delivering HPV test results, physicians are recommended to summarize why the test was performed and contextualize a positive result in a neutral, non-stigmatizing fashion that reinforces the high prevalence and transience of cervical HPV infection, as well as acknowledge potential concerns of transmission to partners. Providing information in print at the time of delivery of results is also recommended.

In delivering HPV results, communication style is highlighted to be as important as the content of the message. CDC guidelines for cervical HPV infection have the following evidence-based recommendations for physicians delivering the diagnosis of cancer (not site-specific): recommend that clinicians slow down, adjust language to the literacy of the patient, supplement facts with stories, anecdotes or pictures, limit the topics covered at each visit, and use the so-called “teach back” method to assess the comprehension of patients at the end of a conversation.14, 15

By analogy, at the time of requesting HPV testing in OSCC, as with any diagnostic test, providing both verbal and print education may result in improved communication and understanding (see brochure provided in Figure 1).16 When sharing with a patient that their OSCC is HPV-positive, providing both verbal and written education may be helpful in light of the questions that sometimes ensue after the initial relief of improved prognosis associated with HPV-OSCC, i.e. sexual intimacy, transmission, and/or infidelity.

Reaction to HPV-positive test

Patients may react differently to finding out their OSCC is HPV-positive, as some may experience anxiety and confusion about the behavioral aspects of infection (i.e. how, when or why they acquired the infection). The NCCN panel for head and neck cancers acknowledges that HPV testing of OSCC may lead to questions regarding prognosis and sexual history, which clinicians should be prepared to discuss.7 In its discussion of HPV infection, the NCCN panel cautions “ HPV information may add anxiety and stress for some patients. Alternatively, gaining an understanding of the etiology for one’s cancer can result in reduced anxiety for some patients.”7

Based upon the cervical literature, patients presented with a diagnosis of cervical cancer (the overwhelming majority of which are HPV-related) have significant psychosocial sequelae including anxiety, depression, and sexual dysfunction.17 It has been suggested that psychosocial counseling in this patient population may lead to improvement in quality of life.18 Women who are diagnosed with a cervical HPV infection and/or premalignant lesions have been found to report self-blame, grief, concern, anxiety, shock, fear, shame, sexual dysfunction, and distress.19, 20 Commonly, women express concerns regarding disclosure of results to partner or partners, fear of future transmission, partner rejection, and questions over the source of infection.14, 21, 22 Individuals report angst about the underlying infection that cannot be treated, the stigma of STI, and questions regarding progression from infection to cervical pre-malignancy and/or malignancy. Along with clinical counseling, addressing patients’ behavioral questions may help to reduce the aforementioned psychological sequelae of this complex diagnosis. Patients experience emotional reactions at the time of a cancer diagnosis which may interfere with comprehension,23 and these issues may be amplified with the additional diagnosis of HPV.

Below we discuss common patient questions and what is known and unknown in response to these questions

(1) How did I get an oral HPV infection?

  • HPV is a sexually transmitted infection that can infect the epithelium of the oropharynx, oral cavity, and anogenital tract.24

  • Genital HPV natural history is well understood and serves as the paradigm against which we compare oral HPV natural history. Genital HPV infections, including cervical, vaginal, and penile infection, are common among sexually active young adults. More than 80% of sexually active young adults are infected with a genital HPV infection at some point during their lifetime, although many of these people will never know they were infected.25, 26 Most people clear these genital infections within a year or two on their own.25, 27 Among those who do not clear their infections, persistent infection can lead to pre-malignant and malignant genital lesions.2830

  • Oral HPV infection is significantly less common than genital HPV infection, and infections are more common among men than among women.3135 Initial studies suggest that most people clear their oral HPV infections within a year or two on their own, but some oral HPV infections persist.36, 37

  • Oral HPV infection is more common in individuals who have ever performed oral sex, and who have a higher number of lifetime and recent oral sexual partners.31, 38, 39 However, oral HPV infection has also been (more rarely) detected in some people who report never performing oral sex.31, 37, 38, 40

  • Oral HPV infection is also more likely to be found in individuals with higher number of lifetime and/or recent vaginal sex partners. Many sexual behaviors are related and on average, people who have a high number of sexual partners for one act have higher numbers of partners for other acts as well (i.e. the relevant sexual exposures are collinear).31

  • The presence of oral HPV infection is not a marker of promiscuity. Some people with an oral HPV infection report never having performed oral sex, or have only had a few lifetime oral sex partners.31, 38, 39, 41 Current estimates indicate that about 10% of all men and 4% of all women ages 14–69 in the general U.S. population have a prevalent oral HPV infection.31 It is believed, though it has not been shown, that many more sexually active individuals are exposed to oral HPV infection in their lifetime,36, 37, 42 although some people may never have an oral HPV infection.

(2) Are oral HPV and HPV-positive head and neck cancers caused by oral sex?

As summarized below, studies consistently show that oral sex is strongly associated with oral HPV infection and increased odds of HPV-OSCC.

  • Oral-genital contact:
    • Several studies have shown that individuals with a higher number of oral sex partners are more likely to have:
      • Prevalent oral HPV infection38, 39
      • Incident oral HPV infection43
      • HPV-associated head and neck cancer44, 45
    • This suggests that HPV is likely transmitted by oral sex. However, it is important to understand that many sexual behaviors are collinear (i.e. people with higher numbers of partners for one type of sexual behavior often have higher numbers of partners for other types of behavior).
      Therefore, it is difficult to determine which behaviors specifically are responsible for the presence of HPV in the mouth and/or pharynx.
  • Oral-anal contact:
    • Anal HPV is common and it is possible that oral-anal sexual contact (rimming) may be associated with transmission of oral HPV.4648
    • One study of gay men showed that an increased number of rimming partners is associated with higher oral HPV prevalence49; however, further research is needed to conclusively elucidate the role of rimming in oral HPV transmission.
  • Oral-oral contact:
    • It is not known whether open-mouth kissing (i.e. deep kissing or French kissing) can transmit oral HPV infection. Three studies reported an association between open-mouth kissing and oral HPV prevalence, even among those who reported never having performed oral sex.31, 38, 50 However, these studies were limited by small sample sizes and could be explained by confounding or mis-reporting of behavior. Other studies have not found any associations with kissing.49, 51 Oral HPV has been detected in youth, but prevalence among younger adolescents (12–15 years old, 1.5%) and older adolescents (16–20 year olds, 3.3%) is relatively low despite the common practice of deep-kissing among these populations.40, 52

(3) When did I get an oral HPV infection?

  • We do not know the time from the acquisition of an oral HPV infection to the time of diagnosis with HPV-OSCC. However, extrapolating from what is known about anogenital HPV natural history we believe that individuals presenting with HPV-OSCC today likely acquired these infections many years (possibly decades) previously.53, 54

  • Oral HPV infection is not only detected in individuals in their 20s, at the peak time of sexual activity for most individuals, but has even higher prevalence among older age groups.31 In a recent U.S. population-based study, oral HPV prevalence in both men and women was most common among 30–34 year olds (7.3%) and 60–64 year olds (11.4%), though these estimates do not necessarily reflect the time an infection was initially acquired. Whether the second peak in oral HPV prevalence among 60–64 year olds is related to recent sexual activity, presence of pre-cancer, immune-related factors (i.e re-activation) or generational differences, is presently unknown.

  • We expect that oral HPV infection must persist for many years for cancer to occur, though the data we currently have on natural history of oral HPV infection is limited.53, 54 A recent study detected antibodies to HPV oncogene E6 in HPV-OSCC cases more than 10 years before cancer was diagnosed, while a nested case control study in Nordic countries found HPV16 antibodies 15 years or more prior to diagnosis.53 These studies suggest that oral HPV infections were acquired many years before development and diagnosis of malignancy. However, we do not know exactly how long it takes for HPV to cause oropharyngeal cancer.

(4) Does diagnosis of HPV-OSCC indicate past or present promiscuity?

  • It is important to remind patients that being diagnosed with HPV-OSCC does not imply that either partner was/is unfaithful. Based upon CDC recommendations for discussion of presence of an oncogenic cervical HPV infection, “emphasis should be placed on the fact that HPV is a common infection that is often shared between partners and can lie dormant for many years.”13

  • An HPV-OSCC diagnosis does not imply that either partner has a “risky” sexual past. Although HPV-OSCC is strongly associated with sexual behaviors and with a higher number of lifetime sexual partners, many patients have a modest number of lifetime sexual partners.45, 55 Indeed, while a higher number of sexual partners increases one’s odds (chances) of acquiring a sexually transmitted infection such as HPV, and thus is associated with increased odds of HPV-OSCC, it only takes one partner who is infected to acquire the infection.44 Around half of HPV-OSCC patients have had five or fewer lifetime oral sex partners and some report never having performed oral sex.4

  • While not as common as genital HPV infections, many people will likely have been exposed to oral HPV infection during their lifetime.31 We suspect that while many people are exposed to oral HPV infection, few become infected and even fewer develop into malignancy.

(5) Will I transmit this infection to others?

  • Transmission to family and friends:
    • Oral HPV does not appear to be casually transmitted.
    • There is currently no evidence for non-sexual transmission of oncogenic HPV to the mouth, except for the possibility that it may be transmitted through open-mouth kissing.
  • Transmission to spouse or long-term sexual partners:
    • HPV is a sexually transmitted infection – couples that have been intimate have likely already exposed each other to their sexual infections.56 Therefore, we do not recommend changing current sexual behaviors in established relationships.
    • Spouses of patients with HPV-OSCC have likely been exposed to HPV themselves (from current and/or former partners), though they usually do not have detectable oral HPV infection (D’Souza, unpublished results). Thus, there is no need to change sexual behavior with a current spouse or long-term partners.
    • Female patients with HPV-OSCC and female spouses/partners of patients with HPV-OSCC should undergo routine cervical screening per NCCN guidelines (as currently indicated for all women over 21 years of age).57
  • Transmission to future partners:
    • Many patients with HPV-OSCC do not have detectable viral infection after treatment and therefore likely cannot transmit the infection after therapy.58 On the other hand, some patients continue to have HPV detectable in exfoliated oral cells after therapy.58
    • There is a possible risk of transmission to future partners, though the level of risk is not known.
    • As is the case for prevention of any sexually transmitted infection, discussion of appropriate protection is advised with new partners.
    • Inconsistent condom use or lack of condom use and barrier protection during oral-genital and genital-genital contact has been associated with increased odds of oral HPV infection and HPV-OSCC.31, 44, 59 The use of barriers during new sexual encounters may decrease the risk of transmitting genital HPV infection to the mouth during oral sex.60 Research has not yet evaluated whether oral HPV infection can be transmitted to the genital area during oral sex.

(6) Is my spouse/partner at increased risk of this cancer? What should they do?

  • Some studies have suggested that spouses of cervical cancer patients are at ~2–3 fold increased risk of HPV-OSCC.6163 There are also a limited number of case reports in the literature of couples where both members were diagnosed with HPV-OSCC.64

  • Partners of patients with HPV-OSCC may have slightly higher rates of HPV-associated cancers such as anal, penile, and/or oropharyngeal than the general population, but these are still rare cancers and the chances of developing these cancers remain low overall.65 Cervical pre-cancerous lesions are more common among female spouses.63 Women with HPV-OSCC or female partners of HPV-OSCC patients should follow cervical cancer screening guidelines.57

  • There are presently no screening guidelines for HPV-associated malignancies of the head and neck. Therefore, with the exception of cervical cancer screening guidelines, there are no additional recommendations for sexual partners or spouses of patients of HPV-OSCC specifically regarding head and neck cancer.

  • In the context of genital HPV, the CDC recommends that both patients and partners receive counseling which addresses the potential psychological and sexual issues that arise with the diagnosis of a lesion that is associated with HPV.13 Physicians of patients and partners diagnosed with genital HPV infection are recommended to acknowledge tension regarding past experiences, effect on present intimacy and other practical solutions to cope with the tension, which may arise from the diagnosis of HPV.13, 66 However, it should be noted that partner notification is voluntary (analogous to other sexually transmitted infections such as HIV). Indeed, as these HPV infections were acquired many years previously and most individuals clear HPV infections on their own, there are no clear guidelines for partner notification. Partner notification could pose more harm than benefit. In the CDC’s counseling messages for genital HPV, the potential for negative partners reactions (rejection and abuse) are highlighted.

  • An oropharyngeal “Pap-test equivalent” has recently been evaluated in high-risk populations, though the study suggests it may not be useful for early detection of oropharyngeal cancers.67 More research is needed to explore viable secondary prevention mechanisms for oropharyngeal cancers.

(7) Will I always have this oral HPV infection?

  • Before treatment, many patients with HPV-OSCC have HPV DNA detectable in their oral exfoliate cells; this DNA is likely sloughed off from the tumor and does not necessarily represent a virus capable of infecting someone else.44, 58, 65

  • After treatment, some patients no longer have HPV DNA detectable in their oral exfoliate cells, while others do. We do not know whether the infection is “cleared” (gone) or “latent” (controlled by the immune system but not eliminated).58

(8) What does being HPV-positive mean about my disease?

  • Patients diagnosed with HPV-OSCC have significantly better overall survival than patients with HPV-negative OSCC.5, 6 Three-year overall survival for patients with HPV-OSCC is 82% as opposed to 57% among HPV-negative OSCC patients.5 In population-level data in the U.S., more than half of HPV-OSCCs were alive ten years after diagnosis.1

  • Patients with HPV-OSCC also have improved progression-free survival.6 The improved prognosis of HPV-associated tumors is believed to be due to increased radiosensitivity conferred by HPV.68

  • Given this strong prognosis, current trials are evaluating therapy de-escalation, with the hope that side effects from treatment could be reduced without compromising survival; however, we do not yet know the results of these trials.

  • It should be highlighted that current NCCN guidelines caution against the use of HPV tumor status in clinical decision making outside the context of a clinical trial.7

(9) Does current or past tobacco use affect oral HPV infection and HPV-OSCC?

  • Current tobacco use has been associated with increased prevalence of oral HPV infection in several studies, suggesting that it may increase either the likelihood of becoming infected when exposed or increase the persistence of oral HPV infection.31, 49, 69

  • Current tobacco use and cumulative exposure to tobacco have been associated with worse prognosis after adjusting for HPV tumor status. Smoking is associated with increased chance of death and locoregional progression for both HPV-positive and HPV-negative OSCC.70

  • These data suggest that tobacco cessation is an important component of counseling.

(10) Can the HPV vaccines help?

  • There are currently two HPV vaccines licensed to prevent new HPV infections in the U.S. The quadrivalent HPV vaccine (Gardasil, made by Merck) protects against HPV types 6, 11, 16, and 18. The bivalent HPV vaccine (Cervarix, made by GSK) protects against HPV types 16 and 18. Both vaccines are currently recommended for all girls and boys around 11–12 years old, as well as “catch-up” vaccination of individuals up to 26 years of age who have not been vaccinated.71, 72

  • HPV vaccines prevent individuals from becoming infected with these HPV types if/when they are exposed to the virus.73, 74 These vaccines are designed to be administered before sexual debut, i.e. before exposure to the HPV types targeted. Unfortunately, these vaccines do not help individuals clear an infection they have already acquired prior to vaccination.

  • The efficacy of these vaccines in prevention of oral HPV infection has not been evaluated. Existing clinical trials of the HPV vaccines have focused on their impact on HPV-associated anogenital diseases like cervical and anal cancer, and their utility against oral HPV infection is unknown.73, 74 However, given that such a high proportion of head and neck cancers are caused by HPV16 (which the vaccines target), researchers are hopeful that the vaccine might be beneficial in the prevention of future HPV-OSCC as well.75, 76 Several studies using animal models do suggest that HPV vaccination could provide protection against oral HPV infection with vaccine-type HPV strains.77, 78

  • It is not known whether the vaccines might have an effect on disease recurrence in the oropharynx. Women treated for vulvar or cervical HPV-related lesions during a randomized blinded placebo controlled study of the quadrivalent HPV vaccine were retrospectively analyzed for subsequent disease. Risk of subsequent HPV-related disease was lower among those who received the vaccine the placebo group. While this is seemingly promising, the benefits and risks of vaccination in people with HPV-OSCC are unknown and need further research.79

  • Some patients wonder if their spouse should get the HPV vaccine. Spouses have likely already been exposed to HPV and would therefore likely not benefit from vaccination.

Conclusion

HPV confers a unique demographic and prognostic profile upon patients with OSCC; however, the personal and social implications of this diagnosis have not been studied to date. It is important that we acknowledge the strengths of our current knowledge base as well as the unknowns when we counsel patients regarding this diagnosis. While aspects of oral HPV infection and HPV-OSCC are well understood, there are gaps in our present knowledge base, some of which are of great interest to patients and their partners. Ongoing work in risk factors, natural history, psychosocial effects, and therapies for oral HPV infection and HPV-OSCC will inform counseling guidelines of this patient population.

References

  • 1.Chaturvedi AK, Engels EA, Pfeiffer RM, Hernandez BY, Xiao W, Kim E, et al. Human papillomavirus and rising oropharyngeal cancer incidence in the United States. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2011;29:4294–4301. doi: 10.1200/JCO.2011.36.4596. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Human papillomavirus-associated cancers - United States, 2004–2008. MMWR Morbidity and mortality weekly report. 2012;61:258–261. [PubMed] [Google Scholar]
  • 3.Lingen MW, Xiao W, Schmitt A, Jiang B, Pickard R, Kreinbrink P, et al. Low etiologic fraction for high-risk human papillomavirus in oral cavity squamous cell carcinomas. Oral oncology. 2013;49:1–8. doi: 10.1016/j.oraloncology.2012.07.002. [DOI] [PubMed] [Google Scholar]
  • 4.Gillison ML, D'Souza G, Westra W, Sugar E, Xiao W, Begum S, et al. Distinct risk factor profiles for human papillomavirus type 16-positive and human papillomavirus type 16-negative head and neck cancers. J Natl Cancer Inst. 2008;100:407–420. doi: 10.1093/jnci/djn025. [DOI] [PubMed] [Google Scholar]
  • 5.Ang KK, Harris J, Wheeler R, Weber R, Rosenthal DI, Nguyen-Tan PF, et al. Human papillomavirus and survival of patients with oropharyngeal cancer. The New England journal of medicine. 2010;363:24–35. doi: 10.1056/NEJMoa0912217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Fakhry C, Westra WH, Li S, Cmelak A, Ridge JA, Pinto H, et al. Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trial. J Natl Cancer Inst. 2008;100:261–269. doi: 10.1093/jnci/djn011. [DOI] [PubMed] [Google Scholar]
  • 7.Pfister DG, Ang K-K, Brizel DM, Gillison ML, Lydiatt WM, Shah JP, et al. NCCN Practice Guidelines for Head and Neck Cancers. Oncology (Williston Park) 2012 [PubMed] [Google Scholar]
  • 8.Weaver KE, Danhauer SC, Tooze JA, Blackstock AW, Spangler J, Thomas L, et al. Smoking cessation counseling beliefs and behaviors of outpatient oncology providers. The oncologist. 2012;17:455–462. doi: 10.1634/theoncologist.2011-0350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Schnoll RA, Zhang B, Rue M, Krook JE, Spears WT, Marcus AC, et al. Brief physician-initiated quit-smoking strategies for clinical oncology settings: a trial coordinated by the Eastern Cooperative Oncology Group. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2003;21:355–365. doi: 10.1200/JCO.2003.04.122. [DOI] [PubMed] [Google Scholar]
  • 10.Thorndike AN, Rigotti NA, Stafford RS, Singer DE. National patterns in the treatment of smokers by physicians. JAMA : the journal of the American Medical Association. 1998;279:604–608. doi: 10.1001/jama.279.8.604. [DOI] [PubMed] [Google Scholar]
  • 11.Kottke TE, Brekke ML, Solberg LI, Hughes JR. A randomized trial to increase smoking intervention by physicians. Doctors Helping Smokers, Round I. JAMA : the journal of the American Medical Association. 1989;261:2101–2106. [PubMed] [Google Scholar]
  • 12.Zabora J, BrintzenhofeSzoc K, Curbow B, Hooker C, Piantadosi S. The prevalence of psychological distress by cancer site. Psycho-oncology. 2001;10:19–28. doi: 10.1002/1099-1611(200101/02)10:1<19::aid-pon501>3.0.co;2-6. [DOI] [PubMed] [Google Scholar]
  • 13.Dunne EF, Friedman A, Datta SD, Markowitz LE, Workowski KA. 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–S152. doi: 10.1093/cid/cir703. [DOI] [PubMed] [Google Scholar]
  • 14.Anhang R, Goodman A, Goldie SJ. HPV communication: review of existing research and recommendations for patient education. CA: a cancer journal for clinicians. 2004;54:248–259. doi: 10.3322/canjclin.54.5.248. [DOI] [PubMed] [Google Scholar]
  • 15.Davis TC, Williams MV, Marin E, Parker RM, Glass J. Health literacy and cancer communication. CA: a cancer journal for clinicians. 2002;52:134–149. doi: 10.3322/canjclin.52.3.134. [DOI] [PubMed] [Google Scholar]
  • 16.Petrie KJ, Muller JT, Schirmbeck F, Donkin L, Broadbent E, Ellis CJ, et al. Effect of providing information about normal test results on patients' reassurance: randomised controlled trial. BMJ. 2007;334:352. doi: 10.1136/bmj.39093.464190.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Herzog TJ, Wright JD. The impact of cervical cancer on quality of life--the components and means for management. Gynecologic oncology. 2007;107:572–577. doi: 10.1016/j.ygyno.2007.09.019. [DOI] [PubMed] [Google Scholar]
  • 18.Nelson EL, Wenzel LB, Osann K, Dogan-Ates A, Chantana N, Reina-Patton A, et al. Stress, immunity, and cervical cancer: biobehavioral outcomes of a randomized clinical trial [corrected] Clinical cancer research : an official journal of the American Association for Cancer Research. 2008;14:2111–2118. doi: 10.1158/1078-0432.CCR-07-1632. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Kitchener HC, Fletcher I, Roberts C, Wheeler P, Almonte M, Maguire P. The psychosocial impact of human papillomavirus testing in primary cervical screening-a study within a randomized trial. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society. 2008;18:743–748. doi: 10.1111/j.1525-1438.2007.01113.x. [DOI] [PubMed] [Google Scholar]
  • 20.Pirotta M, Ung L, Stein A, Conway EL, Mast TC, Fairley CK, et al. The psychosocial burden of human papillomavirus related disease and screening interventions. Sexually transmitted infections. 2009;85:508–513. doi: 10.1136/sti.2009.037028. [DOI] [PubMed] [Google Scholar]
  • 21.Bell S, Porter M, Kitchener H, Fraser C, Fisher P, Mann E. Psychological response to cervical screening. Preventive medicine. 1995;24:610–616. doi: 10.1006/pmed.1995.1096. [DOI] [PubMed] [Google Scholar]
  • 22.McCaffery K, Waller J, Forrest S, Cadman L, Szarewski A, Wardle J. Testing positive for human papillomavirus in routine cervical screening: examination of psychosocial impact. BJOG : an international journal of obstetrics and gynaecology. 2004;111:1437–1443. doi: 10.1111/j.1471-0528.2004.00279.x. [DOI] [PubMed] [Google Scholar]
  • 23.Doak CC, Doak LG, Friedell GH, Meade CD. Improving comprehension for cancer patients with low literacy skills: strategies for clinicians. CA: a cancer journal for clinicians. 1998;48:151–162. doi: 10.3322/canjclin.48.3.151. [DOI] [PubMed] [Google Scholar]
  • 24.Munoz N, Castellsague X, de Gonzalez AB, Gissmann L. Chapter 1: HPV in the etiology of human cancer. Vaccine. 2006;24(Suppl 3):S3/1–S3/10. doi: 10.1016/j.vaccine.2006.05.115. [DOI] [PubMed] [Google Scholar]
  • 25.Weaver BA. Epidemiology and natural history of genital human papillomavirus infection. The Journal of the American Osteopathic Association. 2006;106:S2–S8. [PubMed] [Google Scholar]
  • 26.Dunne EF, Nielson CM, Stone KM, Markowitz LE, Giuliano AR. Prevalence of HPV infection among men: A systematic review of the literature. The Journal of infectious diseases. 2006;194:1044–1057. doi: 10.1086/507432. [DOI] [PubMed] [Google Scholar]
  • 27.Woodman CB, Collins S, Winter H, Bailey A, Ellis J, Prior P, et al. Natural history of cervical human papillomavirus infection in young women: a longitudinal cohort study. Lancet. 2001;357:1831–1836. doi: 10.1016/S0140-6736(00)04956-4. [DOI] [PubMed] [Google Scholar]
  • 28.Dalstein V, Riethmuller D, Pretet JL, Le Bail Carval K, Sautiere JL, Carbillet JP, et al. Persistence and load of high-risk HPV are predictors for development of high-grade cervical lesions: a longitudinal French cohort study. International journal of cancer Journal international du cancer. 2003;106:396–403. doi: 10.1002/ijc.11222. [DOI] [PubMed] [Google Scholar]
  • 29.Ho GY, Burk RD, Klein S, Kadish AS, Chang CJ, Palan P, et al. Persistent genital human papillomavirus infection as a risk factor for persistent cervical dysplasia. Journal of the National Cancer Institute. 1995;87:1365–1371. doi: 10.1093/jnci/87.18.1365. [DOI] [PubMed] [Google Scholar]
  • 30.Wallin KL, Wiklund F, Angstrom T, Bergman F, Stendahl U, Wadell G, et al. Type-specific persistence of human papillomavirus DNA before the development of invasive cervical cancer. The New England journal of medicine. 1999;341:1633–1638. doi: 10.1056/NEJM199911253412201. [DOI] [PubMed] [Google Scholar]
  • 31.Gillison ML, Broutian T, Pickard RK, Tong ZY, Xiao W, Kahle L, et al. 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]
  • 32.Trottier H, Burchell AN. Epidemiology of mucosal human papillomavirus infection and associated diseases. Public health genomics. 2009;12:291–307. doi: 10.1159/000214920. [DOI] [PubMed] [Google Scholar]
  • 33.D'Souza G, Fakhry C, Sugar EA, Seaberg EC, Weber K, Minkoff HL, et al. Six-month natural history of oral versus cervical human papillomavirus infection. Int J Cancer. 2007;121:143–150. doi: 10.1002/ijc.22667. [DOI] [PubMed] [Google Scholar]
  • 34.Canadas MP, Bosch FX, Junquera ML, Ejarque M, Font R, Ordonez E, et al. Concordance of prevalence of human papillomavirus DNA in anogenital and oral infections in a high-risk population. J Clin Microbiol. 2004;42:1330–1332. doi: 10.1128/JCM.42.3.1330-1332.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Giuliano AR, Lazcano-Ponce E, Villa LL, Flores R, Salmeron J, Lee JH, et al. The human papillomavirus infection in men study: human papillomavirus prevalence and type distribution among men residing in Brazil, Mexico, and the United States. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2008;17:2036–2043. doi: 10.1158/1055-9965.EPI-08-0151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Beachler DC, D'Souza G, Sugar EA, Gillison ML. Differences in oral and anal HPV natural history among HIV-infected individuals; 28th International Papillomavirus Conference; Puerto Rico. 2012. p. 213. [Google Scholar]
  • 37.D'Souza G, Griffioen AM, Kluz N, Gillison ML. Oral HPV prevalence, six-month persistence and incidence among high-risk young adults; 28th International Papillomavirus Conference; Puerto Rico. 2012. p. 215. [Google Scholar]
  • 38.D'Souza G, Agrawal Y, Halpern J, Bodison S, Gillison ML. Oral sexual behaviors associated with prevalent oral human papillomavirus infection. The Journal of infectious diseases. 2009;199:1263–1269. doi: 10.1086/597755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Kreimer AR, Alberg AJ, Daniel R, Gravitt PE, Viscidi R, Garrett ES, et al. Oral human papillomavirus infection in adults is associated with sexual behavior and HIV serostatus. J Infect Dis. 2004;189:686–698. doi: 10.1086/381504. [DOI] [PubMed] [Google Scholar]
  • 40.Smith EM, Swarnavel S, Ritchie JM, Wang D, Haugen TH, Turek LP. Prevalence of human papillomavirus in the oral cavity/oropharynx in a large population of children and adolescents. Pediatr Infect Dis J. 2007;26:836–840. doi: 10.1097/INF.0b013e318124a4ae. [DOI] [PubMed] [Google Scholar]
  • 41.Kreimer AR, Villa A, Nyitray AG, Abrahamsen M, Papenfuss M, Smith D, et al. The epidemiology of oral HPV infection among a multinational sample of healthy men. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2011;20:172–182. doi: 10.1158/1055-9965.EPI-10-0682. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Campbell CMP, Kreimer AR, Lin H-Y, Fulp W, Abrahamsen M, Papenfuss MR, et al. Incidence and clearance of oral oncogenic human papillomavirus (HPV) in men (HIM): a cohort study; 28th International Papillomavirus Conference; Puerto Rico. 2012. p. 214. [Google Scholar]
  • 43.Kero K, Rautava J, Syrjanen K, Grenman S, Syrjanen S. Oral mucosa as a reservoir of human papillomavirus: point prevalence, genotype distribution, and incident infections among males in a 7-year prospective study. European urology. 2012;62:1063–1070. doi: 10.1016/j.eururo.2012.06.045. [DOI] [PubMed] [Google Scholar]
  • 44.D'Souza G, Kreimer AR, Viscidi R, Pawlita M, Fakhry C, Koch WM, et al. Case-control study of human papillomavirus and oropharyngeal cancer. N Engl J Med. 2007;356:1944–1956. doi: 10.1056/NEJMoa065497. [DOI] [PubMed] [Google Scholar]
  • 45.Smith EM, Ritchie JM, Summersgill KF, Klussmann JP, Lee JH, Wang D, et al. Age, sexual behavior and human papillomavirus infection in oral cavity and oropharyngeal cancers. Int J Cancer. 2004;108:766–772. doi: 10.1002/ijc.11633. [DOI] [PubMed] [Google Scholar]
  • 46.Chin-Hong PV, Vittinghoff E, Cranston RD, Buchbinder S, Cohen D, Colfax G, et al. Age-Specific prevalence of anal human papillomavirus infection in HIV-negative sexually active men who have sex with men: the EXPLORE study. J Infect Dis. 2004;190:2070–2076. doi: 10.1086/425906. [DOI] [PubMed] [Google Scholar]
  • 47.Castro FA, Quint W, Gonzalez P, Katki HA, Herrero R, van Doorn LJ, et al. Prevalence of and risk factors for anal human papillomavirus infection among young healthy women in Costa Rica. The Journal of infectious diseases. 2012;206:1103–1110. doi: 10.1093/infdis/jis458. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Nyitray AG, Smith D, Villa L, Lazcano-Ponce E, Abrahamsen M, Papenfuss M, et al. Prevalence of and risk factors for anal human papillomavirus infection in men who have sex with women: a cross-national study. The Journal of infectious diseases. 2010;201:1498–1508. doi: 10.1086/652187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Beachler DC, Weber KM, Margolick JB, Strickler HD, Cranston RD, Burk RD, et al. Risk factors for oral HPV infection among a high prevalence population of HIV-positive and at-risk HIV-negative adults. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2012;21:122–133. doi: 10.1158/1055-9965.EPI-11-0734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Pickard RK, Xiao W, Broutian TR, He X, Gillison ML. The prevalence and incidence of oral human papillomavirus infection among young men and women, aged 18–30 years. Sexually transmitted diseases. 2012;39:559–566. doi: 10.1097/OLQ.0b013e31824f1c65. [DOI] [PubMed] [Google Scholar]
  • 51.Edelstein ZR, Schwartz SM, Hawes S, Hughes JP, Feng Q, Stern ME, et al. Rates and determinants of oral human papillomavirus infection in young men. Sexually transmitted diseases. 2012;39:860–867. doi: 10.1097/OLQ.0b013e318269d098. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Trends in HIV-related risk behaviors among high school students--United States, 1991–2011. MMWR Morbidity and mortality weekly report. 2012;61:556–560. [PubMed] [Google Scholar]
  • 53.Mork J, Lie AK, Glattre E, Hallmans G, Jellum E, Koskela P, et al. Human papillomavirus infection as a risk factor for squamous-cell carcinoma of the head and neck. N Engl J Med. 2001;344:1125–1131. doi: 10.1056/NEJM200104123441503. [DOI] [PubMed] [Google Scholar]
  • 54.Kreimer AR, Johansson M, Waterboer T, Kaaks R, Chang-Claude J, Drogen D, et al. An evaluation of human papillomavirus antibodies and risk of subsequent head and neck cancer; 28th International Papillomavirus Conference; Puerto Rico. 2012. p. 209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Beachler DC, D'Souza G. Nuances in the changing epidemiology of head and neck cancer. Oncology (Williston Park) 2010;24:924–926. [PMC free article] [PubMed] [Google Scholar]
  • 56.Reiter PL, Pendergraft WF, 3rd, Brewer NT. Meta-analysis of human papillomavirus infection concordance. Cancer epidemiology, biomarkers & prevention: a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2010;19:2916–2931. doi: 10.1158/1055-9965.EPI-10-0576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Saslow D, Solomon D, Lawson HW, Killackey M, Kulasingam SL, Cain J, et al. American Cancer Society, American Society for Colposcopy and Cervical Pathology, and American Society for Clinical Pathology screening guidelines for the prevention and early detection of cervical cancer. CA: a cancer journal for clinicians. 2012;62:147–172. doi: 10.3322/caac.21139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Agrawal Y, Koch WM, Xiao W, Westra WH, Trivett AL, Symer DE, et al. Oral human papillomavirus infection before and after treatment for human papillomavirus 16-positive and human papillomavirus 16-negative head and neck squamous cell carcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research. 2008;14:7143–7150. doi: 10.1158/1078-0432.CCR-08-0498. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Coutlee F, Trottier AM, Ghattas G, Leduc R, Toma E, Sanche G, et al. Risk factors for oral human papillomavirus in adults infected and not infected with human immunodeficiency virus. Sex Transm Dis. 1997;24:23–31. doi: 10.1097/00007435-199701000-00006. [DOI] [PubMed] [Google Scholar]
  • 60.Winer RL, Hughes JP, Feng Q, O'Reilly S, Kiviat NB, Holmes KK, et al. Condom use and the risk of genital human papillomavirus infection in young women. The New England journal of medicine. 2006;354:2645–2654. doi: 10.1056/NEJMoa053284. [DOI] [PubMed] [Google Scholar]
  • 61.Huang LW, Seow KM. Oral sex is a risk factor for human papillomavirus-associated nasopharyngeal carcinoma in husbands of women with cervical cancer. Gynecologic and obstetric investigation. 2010;70:73–75. doi: 10.1159/000291199. [DOI] [PubMed] [Google Scholar]
  • 62.Hemminki K, Dong C. Cancer in husbands of cervical cancer patients. Epidemiology. 2000;11:347–349. doi: 10.1097/00001648-200005000-00022. [DOI] [PubMed] [Google Scholar]
  • 63.Hemminki K, Dong C, Frisch M. Tonsillar and other upper aerodigestive tract cancers among cervical cancer patients and their husbands. Eur J Cancer Prev. 2000;9:433–437. doi: 10.1097/00008469-200012000-00010. [DOI] [PubMed] [Google Scholar]
  • 64.Haddad R, Crum C, Chen Z, Krane J, Posner M, Li Y, et al. HPV16 transmission between a couple with HPV-related head and neck cancer. Oral Oncol. 2008;44:812–815. doi: 10.1016/j.oraloncology.2007.09.004. [DOI] [PubMed] [Google Scholar]
  • 65.Capone RB, Pai SI, Koch WM, Gillison ML, Danish HN, Westra WH, et al. Detection and quantitation of human papillomavirus (HPV) DNA in the sera of patients with HPV-associated head and neck squamous cell carcinoma. Clin Cancer Res. 2000;6:4171–4175. [PubMed] [Google Scholar]
  • 66.Graziottin A, Serafini A. HPV infection in women: psychosexual impact of genital warts and intraepithelial lesions. The journal of sexual medicine. 2009;6:633–645. doi: 10.1111/j.1743-6109.2008.01151.x. [DOI] [PubMed] [Google Scholar]
  • 67.Fakhry C, Rosenthal BT, Clark DP, Gillison ML. Associations between oral HPV16 infection and cytopathology: evaluation of an oropharyngeal "pap-test equivalent" in high-risk populations. Cancer Prev Res (Phila) 2011;4:1378–1384. doi: 10.1158/1940-6207.CAPR-11-0284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Lambert PF, Yang RZ, Blitzer GC, Smith MA, Armstrong EA, Harari PM, et al. Assessmen of tumor growth rates in response to radiation and chemotherapy treatment in HPV-positive and negative head and neck cancers; 28h International Papillomavirus Conference; Puerto Rico. 2012. p. 92. [Google Scholar]
  • 69.Read TR, Hocking JS, Vodstrcil LA, Tabrizi SN, McCullough MJ, Grulich AE, et al. Oral human papillomavirus in men having sex with men: risk-factors and sampling. PloS one. 2012;7:e49324. doi: 10.1371/journal.pone.0049324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Gillison ML, Zhang Q, Jordan R, Xiao W, Westra WH, Trotti A, et al. Tobacco smoking and increased risk of death and progression for patients with p16-positive and p16-negative oropharyngeal cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2012;30:2102–2111. doi: 10.1200/JCO.2011.38.4099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.FDA licensure of quadrivalent human papillomavirus vaccine (HPV4, Gardasil) for use in males and guidance from the Advisory Committee on Immunization Practices (ACIP) MMWR Morbidity and mortality weekly report. 2010;59:630–632. [PubMed] [Google Scholar]
  • 72.FDA licensure of bivalent human papillomavirus vaccine (HPV2, Cervarix) for use in females and updated HPV vaccination recommendations from the Advisory Committee on Immunization Practices (ACIP) MMWR Morbidity and mortality weekly report. 2010;59:626–629. [PubMed] [Google Scholar]
  • 73.Harper DM, Franco EL, Wheeler CM, Moscicki AB, Romanowski B, Roteli-Martins CM, et al. Sustained efficacy up to 4.5 years of a bivalent L1 virus-like particle vaccine against human papillomavirus types 16 and 18: follow-up from a randomised control trial. Lancet. 2006;367:1247–1255. doi: 10.1016/S0140-6736(06)68439-0. [DOI] [PubMed] [Google Scholar]
  • 74.Garland SM, Hernandez-Avila M, Wheeler CM, Perez G, Harper DM, Leodolter S, et al. Quadrivalent vaccine against human papillomavirus to prevent anogenital diseases. N Engl J Med. 2007;356:1928–1943. doi: 10.1056/NEJMoa061760. [DOI] [PubMed] [Google Scholar]
  • 75.Gillison ML. Human papillomavirus-related diseases: oropharynx cancers and potential implications for adolescent HPV vaccination. The Journal of adolescent health : official publication of the Society for Adolescent Medicine. 2008;43:S52–S60. doi: 10.1016/j.jadohealth.2008.07.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.D'Souza G, Dempsey A. The role of HPV in head and neck cancer and review of the HPV vaccine. Preventive medicine. 2011;53(Suppl 1):S5–S11. doi: 10.1016/j.ypmed.2011.08.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Rose RC, Lane C, Wilson S, Suzich JA, Rybicki E, Williamson AL. Oral vaccination of mice with human papillomavirus virus-like particles induces systemic virus-neutralizing antibodies. Vaccine. 1999;17:2129–2135. doi: 10.1016/s0264-410x(98)00484-8. [DOI] [PubMed] [Google Scholar]
  • 78.Suzich JA, Ghim SJ, Palmer-Hill FJ, White WI, Tamura JK, Bell JA, et al. Systemic immunization with papillomavirus L1 protein completely prevents the development of viral mucosal papillomas. Proceedings of the National Academy of Sciences of the United States of America. 1995;92:11553–11557. doi: 10.1073/pnas.92.25.11553. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Joura EA, Garland SM, Paavonen J, Ferris DG, Perez G, Ault KA, et al. Effect of the human papillomavirus (HPV) quadrivalent vaccine in a subgroup of women with cervical and vulvar disease: retrospective pooled analysis of trial data. BMJ. 2012;344:e1401. doi: 10.1136/bmj.e1401. [DOI] [PMC free article] [PubMed] [Google Scholar]

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