HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Mayeaux, E. J. PubMed PubMed Citation Articles by Mayeaux, E. J., Jr

Address correspondence to Edward John Mayeaux, Jr, MD, Department of Family Medicine, Louisiana State University Health Sciences Center, 1501 Kings Highway, Shreveport, LA 71103-4228. E-mail: EMayea{at}lsuhsc.edu.

Human papillomavirus (HPV) infection is a common sexually transmitted infection that is often acquired at the onset of sexual activity. Risk factors include younger age at time of sexual debut, sexual behavior, intact foreskin, and immunologic status. Persistent infection with high-risk oncogenic HPV types (especially 16 and 18) is associated with cervical cancer, other anogenital diseases, as well as some head and neck cancers. Infection with low-risk HPV types is associated with genital warts, low-grade dysplasias, and recurrent respiratory papillomatosis. Screening and management of HPV-related diseases incur high healthcare costs. Whereas routine screening of female patients with Papanicolaou tests helps prevent advanced stages of cancer through early detection and treatment, the recently developed HPV L1 capsid protein virus-like particle vaccines offer an option for prevention of HPV-related diseases, including cervical cancer.

This review provides the latest thinking and data related to HPV. Many presentations at symposia may discuss conditions or diseases that physicians do not often see, especially in primary care–type practices. However, HPV is not one of those entities. Current estimates show that approximately 20 million people are infected with HPV in the United States.¹ The annual incidence of sexually transmitted HPV infection is 6.2 million.² In 2005, an estimated 10,370 new infections and 3710 deaths occurred.³ Worldwide HPV infection is a major issue as well.

The cost for treating persons with HPV infection, preventing HPV infection, and preventing the sequelae of HPV-related diseases is greater than the combined cost for the prevention and treatment of the next three most prevalent sexually transmitted diseases (STDs). In the United States, the total direct medical expenditures for HPV, at $1.6 million annually,⁴ are the highest of all other STDs except the human immunodeficiency virus infection.

During their lifetime, about 75% of sexually active individuals will be exposed to HPV.⁴ One of the most common STDs is genital warts, with 1.4 million individuals (1%) currently affected, and the incidence is increasing.⁵

	Genital Warts

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
Between 500,000 and 1 million new cases of genital warts occur annually in the United States,^6,7 and approximately 316,000 initial office visits in the United States are for genital warts.⁷ A high number occurs in the later teenaged and early college-aged population. Genital warts, like most warts, have about a 3-month latent epithelial phase. In a study by Winer et al,⁸ visible, obvious condylomata acuminata (genital warts) developed in about two thirds of women within 3 years from first sexual intercourse and exposure to HPV type 6 or HPV type 11. The median time to progression from infection to overt clinical warts was 2.9 months, and the median time to wart clearance in response to treatment was 5.9 months. Therefore, changing the paradigms for transmission and prevention of genital warts could make a great difference.

Most HPV is spread by sexual contact. Therefore, proscribing sexual contact obviously would prevent HPV transmission. Compliance with abstinence, however, would be difficult to achieve, especially among teenagers. It is also known that even with abstinence, some documented cases of fomite transmission have occurred, as infection with HPV can be spread by other means (ie, fingers, tampons, swabs, biopsy forceps, and other devices).⁹ Also, documented cases of nonpenetrative sexual activity have been implicated as a cause of genital warts.¹⁰

Unfortunately, many teenagers may be confused about what constitutes "having sexual relations" and "not having sexual relations." Cancer can occur in the throat; so clearly, oral sex also is a means of HPV transmission. It is therefore essential to use clear definitions when determining which individuals or populations are at risk for HPV-associated diseases. Although nonsexual routes of HPV transmission exist, the sexual route is by far the most common. Transmission of HPV infection does not require penetrative intercourse.^10,11

	Diagnosis of Genital Warts

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
Visual inspection with magnification is usually sufficient for diagnosing genital warts. Acetic acid application is insensitive and nonspecific and should not be used for routine screening or diagnosis. It is used mainly for identifying cervical lesions for biopsy. Biopsy is rarely necessary, but it should be done if diagnosis is in doubt, the patient is immunocompromised, the lesion worsens with therapy, or the lesion is pigmented or fixed.¹²

	Treatment Options for Genital Warts

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
The patient may self-treat with topical application of podofilox or imiquimod. Modalities administered by a physician include the following:

• cryotherapy, recommended for vaginal, anal, and oral warts
  
• podophyllin resin
  
• trichloroacetic or bichloroacetic acid, recommended for vaginal and anal warts
  
• surgery (shave biopsy, laser, electrocautery), recommended for anal, vulvar, and oral warts.
  

All these modalities have 60% to 80% short-term efficacy and high rates of recurrence. Their effect on transmission is unknown.¹²

	Diagnosis of Cervical Abnormalities

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
Cytology (Papanicolaou [Pap] smear test) is a useful screening test for detecting cervical dysplasia. It provides indirect evidence of HPV infection because it detects squamous epithelial cell changes typically caused by HPV.¹³ The US Food and Drug Administration has approved high-risk HPV testing for triaging women with atypical cells of undermined significance (ASCUS) detected with the Pap test¹³ and as an addition to the Pap test for cervical cancer screening in women 30 years or older.¹⁴ This test is unnecessary for women who have had a Pap test finding of low-grade squamous intraepithelial lesion (LSIL) or high-grade squamous intraepithelial lesion (HSIL) because we know most are infected with HPV.¹⁴

Currently in the United States, testing for high-risk HPV is done in two major settings. One is a reflex test used when a Pap test shows ASCUS. Newly recommended is high-risk testing. Women who have both tests showing no abnormality can be reliably screened at 3-year intervals because of the high negative predictive value of negative HPV tests combined with cytology.

About 25% of the HPV-infected population has no evidence of infection, whereas the largest proportion of the 75% of sexually active individuals with HPV infection comprise those who have serologic evidence (ie, antibodies to HPV) of having been infected sometime in the past but who do not currently have active infection.

Many women have HPV infection detected by colposcopy, the use of which is determined by the findings of the physical examination and Pap test (exclusive of HPV test findings).¹⁴ When a woman has a Pap test showing abnormal cells, follow-up biopsy is used to histologically establish the level of disease.

Indications for cervical biopsy include visible exophytic lesions on the cervix, an HSIL Pap test result, a Pap test showing atypical squamous cells that cannot exclude HSIL, or LSIL with abnormal colposcopic findings.^12,13

	Treatment Options for Cervical Abnormalities

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
Treatment options for patients with cervical abnormalities start with observation. Cryotherapy may be used to destroy precancerous lesions by freezing them with a metal probe. The loop electrosurgical excision procedure (LEEP) is another option, in which an electric current is passed through a thin wire loop to act as a very sharp knife. Laser therapy directs a narrow beam of intense light to destroy or remove abnormal cells. In cervical conization, or cone biopsy, a knife, laser, or LEEP probe is used to remove a cone-shaped piece of tissue from the center of the uterine cervix.

	Transmission of Human Papillomavirus

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
One medical myth is that once individuals have had sex, they will automatically have an HPV infection. The median number of sexual partners that an individual must have to reach the 50% infection mark for a particular HPV type is four to five. If young male patients are given this information, they will likely think, "I could have four partners, and I'll be safe." Of course, that conclusion is erroneous. One's personal risk is determined by one's choice of a sexual partner. For specific populations, it takes more exposures on average to reach the 50% infection rate. That myth about four to five sexual partners is important in the discussion regarding the design of studies, particularly regarding inclusion and exclusion criteria, by Susan L. Hendrix, DO, in this supplement.

View larger version (17K): [in this window] [in a new window]   Figure 1. Common genotypes of human papillomavirus that are associated with benign and malignant disease. *Koutsky LA, et al. Epidemiol Rev. 1988;10:122-163. Muñoz N, et al. N Engl J Med. 2003;348:518-527. Wiatrak BJ. Curr Opin Otolaryngol Head Neck Surg. 2003;11:433-441.

Once individuals become sexually active, the incidence of HPV infection increases. In a study looking at a collegeaged population, it was found that once sexual activity was initiated—even without intromissive intercourse—the incidence of infection increased over time.¹¹

	Human Papillomavirus Types

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
There exist high-risk, or oncogenic, genotypes of HPV, and low-risk, or benign, genotypes of HPV (Figure 1). Basically, HPVs are categorized into groups based on the sequences of certain proteins, mainly the L1 protein, which is the major structural protein in the viral coat. The vaccine-type virus-like particles and the live virus look alike on the outside.

With wild-type HPV infection, an individual who is exposed to a certain type (eg, HPV 16) will become immune to that type, without having immunity to other HPV types. Thus, each HPV-type infection is almost a different disease as far as its effect on the body.

Some types of HPV have a greater association with cancer than others, whereas some HPV types, mainly types 6 and 11, generally do not cause cancer. However, they can still cause disease. These HPV types are only slightly associated with cancer, mainly vulvar cancer.

Type 6 and type 11 HPV cause an extremely rare, but serious, syndrome termed recurrent respiratory papillomatosis (RRP). Although only about 3000 cases occur per year in the United States, RRP is a devastating disease. Treatment of children with RRP requires multiple ablations and noxious chemicals placed in the airway to control the disease until such time as these children can outgrow the disease.

Juvenile onset of RRP is thought to be the result of vertical transmission from HPV-infected mothers to infants during delivery.¹⁷ Adult onset occurs less frequently and is the result of transmission through sexual contact.¹⁸

Condoms may not be universally effective in preventing HPV-associated cervical dysplasia but may prevent genital warts.¹⁹

	HPV-Related Cancers

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
The two HPV types posing the highest risk associated with cervical cancer are HPV 16 and HPV 18. Figure 1 shows the common HPV types associated with malignant disease. The top five high-risk HPV types are 16, 18, 31, 33, and 45, with HPV 16 and HPV 18 causing the greatest proportion of cervical cancer worldwide. Minor variations occur in prevalence of HPV types from country to country. In general, the ranking of these types holds fairly true.

Vaginal and vulvar cancers are also associated with HPV infections, and other sites of malignant involvement also have been identified. An extremely rare cancer of the nail fold and some oropharyngeal cancers are related to HPV 16. New data have shown HPV 16 is associated with up to 70% of lower tongue and pharyngeal cancers.²⁰ Clearly, the HPV in general is involved in malignant disease in multiple regions. Data, however, are still insufficient to determine exactly how effective any particular preventive methods or treatment modalities will be for these cancers. More interesting information and advances are likely to be forthcoming.

View larger version (37K): [in this window] [in a new window]   Figure 2. Potential cofactors in cervical carcinogenesis. *Smith JS, et al. J Infect Dis. 2002:185:324-331. Castellsagué X, Muñoz N. J Natl Cancer Inst Monogr. 2003;31:20-28. Moscicki AB. J Adolesc Health. 2005; 37(6 suppl):S3-S9.

For the past 20 years, attempts to reduce morbidity and mortality have been unsuccessful. Healthcare providers have reached the limits of the tests and of patients' willingness to undergo the tests. The numbers are remaining constant despite the introduction of new approaches, automated Pap test readers, and new Pap test techniques. Inventing or developing a slightly better version of techniques that physicians are already using will not be sufficient to accomplish increased longevity and life expectancy and better disease outcomes. To effect such changes requires shifting the paradigm and adopting a totally new approach.

Cervical cancer is directly related to HPV infection, but it is not necessarily sufficient by itself to cause all cervical cancers; 99.7% can be proved related to HPV, the other 0.3%¹¹ is suspected but cannot be proved to be related to HPV. Potential cofactors exist in cervical carcinogenesis (Figure 2).^16,23,24 If cervical cancer is an infectious disease, a new paradigm is warranted, one that parallels the current one for preventing hepatitis B, poliomyelitis, rubella, and other diseases that are becoming less common and having reduced morbidity and mortality in the United States.

Several malignancies are attributable to HPV infection (Figure 3).^25,26 Each year, 6% of 9 million new cases of all cancers worldwide, excluding nonmelanoma skin cancers, and 20% to 24% of all cancers in women in Latin American, South-west Asia, and sub-Saharan Africa are attributable to HPV infection.²⁶

View larger version (51K): [in this window] [in a new window]   Figure 3. Malignancies attributable to human papillomavirus infection. *Walboomers JM, et al. J Pathol. 1999;189:12-19. The Current Status of Development of Prophylactic Vaccines Against Human Papillomavirus Infection. Geneva, Switzerland: World Health Organization; 1999.

	Risk Factors for HPV Transmission

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

View larger version (41K): [in this window] [in a new window]   Figure 4. Factors associated with higher risk. *Ho GY, et al. N Engl J Med. 1998;338: 423-428. Koutsky L, et al. Am J Med. 1997; 102:3-8. Karlsson R, et al. Sex Transm Dis. 1995;22:119-127. Moscicki AB, et al. JAMA. 2001;285:2995-3002. ||Schiffman M, et al. J Natl Cancer Inst Monogr. 2003;31:14-19. ¶Chin-Hong PV. J Infect Dis. 2004;190:2070-2076.

The significance of this pyramid is important when considering risk of HPV transmission because, as the study by Castellsagué et al³² shows, when one partner is monogamous, risk is directly related to previous exposure, but when the partner is not monogamous, risk is multiplied. Figure 4 outlines factors associated with higher risk of HPV transmission.

	Screening and Prevention

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
Vast sums of money are spent in the United States for screening and prevention. Insinga et al³³ examined the healthcare cost of cervical HPV-related disease (in 2002 dollars). Approximately 1 million of the 50 million Pap tests done per year in the United States show an abnormality. The cost of workup for a Pap test showing an HSIL was about $2400.

In a study by Alam and Stiller,³⁴ the total direct costs (including costs of initial and subsequent physician visits) per complete clearance of simple and extensive condylomata acuminata via medical modalities ranged from $424 for podofilox to $6665 for interferon-alfa 2b. The direct costs for surgical modalities ranged from $285 to $951.³⁴ Thus, effective prevention of HPV-related disease—even by reducing the number of abnormalities detected on Pap tests by 10% to 30%—could lead to substantial healthcare cost savings.

Generally, antibodies develop in individuals who are infected with the low-risk types of HPV—types 6 and 11—just as they do in those persons infected with HPV type 1, which causes the common warts of the finger. The same thing commonly occurs in individuals with the high-risk types of HPV, but not always.

The good news is that in most women who become infected with the worst HPV types, the infection clears by itself. The bad news is that no one can predict in which women the infection will clear. Thus, HPV of the high-risk types may persist, and as the infection persists, the virus forms proteins that interfere with DNA transcription, pre-programmed cell death (or apoptosis), and the cell's ability to enter the resting cell phase.

Uncontrolled cell growth, DNA errors, and persistent HPV infection lead to cancer. High-risk types of HPV are known to be associated with cancer. Ability to predict in whom this threat exists would allow directly targeting prevention for those women at highest risk of cancer. However, despite the best diagnostic tests available, research findings, and recognition of immunomodular effects of cofactors (eg, smoking, nutrition, oral contraceptives), physicians still lack such predictive ability.

It was once thought that HPV infections progressed in an orderly fashion to cervical intraepithelial neoplasia grade 1 (CIN-1), next to grade 2 (CIN-2), and then to grade 3 (CIN-3). It is now recognized, however, that CIN-1 and HPV infection are much the same and not where the real risk for cancer lies. Somewhere in CIN-1 HPV infection, one cell becomes abnormal and clones itself and becomes the CIN grades 2 and 3, which ultimately lead to cancer.

New evidence-based algorithms for management of abnormalities detected on Pap tests are now available at http://www.asccp.org.

Genital warts are easier to identify, but if they do not respond to treatment as expected, a tissue biopsy is warranted. If the patient has already been treated for genital warts, it is essential to alert the pathologist to avoid using chemicals that are noxious and alter the appearance of the cell sample.

	Comment

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
Human papillomaviruses are associated with a wide spectrum of disease, ranging from noncancerous lesions to cancer diseases, including invasive and in situ cancers of the cervix, vulva/vagina, anus, and penis, as well as invasive conjunctival and tonsillar cancers. All treatment of patients with HPV infection is directed toward high-grade disease and prevention of cancer disease.

The question has always been, How can we treat patients with HPV-related diseases more effectively? But now, the question has become, How can we prevent these diseases more effectively? The answer may be the HPV L1 capsid protein virus-like particle vaccines. These vaccines are designed to prevent genital infections, genital warts, and anogenital neoplasia. The bivalent and quadrivalent HPV vaccines are not live; they contain no viral DNA, so they are neither infectious nor oncogenic.

	Footnotes

 
This article was developed from a lecture that Dr Mayeaux presented at a symposium held October 3, 2007, at the AOA's 112th Annual Convention and Scientific Seminar in San Diego, Calif. The symposium was supported by an educational grant from Merck & Co, Inc.

Dr Mayeaux discloses that he is a consultant (advisory board) for GlaxoSmithKline and Merck & Co, Inc.

	References

Top Genital Warts Diagnosis of Genital Warts Treatment Options for Genital... Diagnosis of Cervical... Treatment Options for Cervical... Transmission of Human... Human Papillomavirus Types HPV-Related Cancers Risk Factors for HPV... Screening and Prevention Comment References

 
1. Cates W Jr. Estimates of the incidence and prevalence of sexually transmitted diseases in the United States. American Social Health Association. Sex Transm Dis.1999; 26(4 suppl):S2 -S7.[Medline]

2. Steinbrook R. The potential of human papillomavirus vaccines [published correction appears in N Engl J Med. 2006;355:745]. N Engl J Med. 2006;354:1109-1112. Available at: http://content.nejm.org/content/full/354/11/1109. Accessed April 18, 2008.

3. American Cancer Society. Cancer Facts & Figures, 2006. Atlanta, Ga: American Cancer Society; 2006. Available at: http://www.cancer.org/downloads/STT/CAFF2006PWSecured.pdf. Accessed April 18, 2008.

4. The American Social Health Association and Kaiser Family Foundation. STDs in America: How Many Cases and At What Cost? Menlo Park, Calif: 1998. Available at: http://www.ashastd.org/pdfs/std_rep.pdf. Accessed April 18, 2008.

5. Koutsky L. Epidemiology of genital human papilloma virus infection. Am Med.1997; 102(5A):3 -8.

6. Koshiol JE, Laurent SA, Pimenta JM. Rate and predictors of new genital warts claims and genital warts-related healthcare utilization among privately insured patients in the United States. Sex Transm Dis. 2004;31:748 -752.[Medline]

7. Centers for Disease Control and Prevention. Sexually Transmitted Disease Surveillance 2004. Atlanta, Ga: Centers for Disease Control and Prevention; 2005. Available at: http://www.cdc.gov/std/stats04/04pdf/2004SurveillanceAll.pdf. Accessed April 18, 2008.

8. Winer RL, Kiviat NB, Hughes JP, Adam DE, Lee SK, Kuypers JM, et al. Development and duration of human papillomavirus lesions, after initial infection. J Infect Dis.2005; 191:731 -738.[Medline]

9. Ferenczy A, Bergeron C, Richart RM. Human papillomavirus DNA in fomites on objects used for the management of patients with genital human papillomavirus infections. Obstet Gynecol.1989; 74:950 -954.[Abstract/Free Full Text]

10. Marrazzo JM, Koutsky LA, Kiviat NB, Kuypers JM, Stine K. Papanicolaou test screening and prevalence of genital human papillomavirus among women who have sex with women. Am J Public Health. 2001;91: 947-952. Available at: http://www.ajph.org/cgi/reprint/91/6/947. Accessed April 18, 2008.

11. Schiffman M, Kjaer SK. Chapter 2: Natural history of anogenital human papillomavirus infection and neoplasia. J Natl Cancer Inst Monogr. 2003;31:14-19. Available at: http://jncimono.oxford-journals.org/cgi/content/full/2003/31/14. Accessed April 18, 2008.

12. Centers for Disease Control and Prevention. Sexually Transmitted Diseases Guidelines. Atlanta, Ga: Centers for Disease Control and Prevention; 2002. MMWR. 2002:51(No. RR-6):1-84. Available at: http://iier.isciii.es/mmwr/indrr_2002.html. Accessed March 26, 2008.

13. Sawaya GF, Brown AD, Washington AE, Garber AM. Clinical Practice. Current approaches to cervical cancer screening. N Engl J Med. 2001:344;1603 -1607.[Free Full Text]

14. US Food and Drug Administration. FDA approves Expanded Use of HPV Test. March 31, 2003. Available at: http://www.fda.gov/bbs/topics/NEWS/2003/NEW00890.html. Accessed March 26, 2008.

15. Bertram P, Treutner KH, Rübben A, Hauptmann S, Schumpelick V. Invasive squamous-cell carcinoma in giant anorectal condyloma (Buschke-Löwenstein tumor). Langenbecks Arch Chir. 1995;380:115 -118.[Medline]

16. Moscicki AB. Impact of HPV infection in adolescent populations. J Adolesc Health.2005; 37(6 suppl):S3 -S9.

17. Armstrong LR, Preston EJ, Reichert M, Phillips DL, Nisenbaum R, Todd NW, et al. Incidence and prevalence of recurrent respiratory papillomatosis among children in Atlanta and Seattle. Clin Infect Dis. 2000;31:107 -109.[Medline]

18. Freed GL, Derkay CS. Prevention of recurrent respiratory papillomatosis: role of HPV vaccination. Int J Pediatr Otorhinolaryngol. 2006;70:1799 -1803.[Medline]

19. Manhart LE, Koutsky LA. Do condoms prevent genital HPV infection, external genital warts, or cervical neoplasia? A meta-analysis. Sex Transm Dis. 2002;29:725 -735.[Medline]

20. 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. Available at: http://content.nejm.org/cgi/content/full/356/19/1944. Accessed April 18, 2008.

21. Parkin DM, Pisani P, Ferlay J. Global cancer statistics. CA Cancer J Clin. 1999;49:33-64. Available at: http://caonline.amcancersoc.org/cgi/reprint/49/1/33. Accessed April 18, 2008.

22. Centers for Disease Control and Prevention. Report of Editorial Consultants' Meeting. Atlanta, Ga: Centers for Disease Control and Prevention, US Department of Health and Human Services;1999 .

23. Smith JS, Muñoz N, Herrero R, Eluf-Neto J, Ngelangel C, Franceschi S, et al. Evidence for Chlamydia trachomatis as a human papillomavirus cofactor in the etiology of invasive cervical cancer in Brazil and the Philippines. J Infect Dis.2002 :185:324 -331.[Medline]

24. Castellsagué X, Muñoz N. Chapter 3: Cofactors in human papillomavirus carcinogenesis—role of parity, oral contraceptives, and tobacco smoking. J Natl Cancer Inst Monogr. 2003;31:20-28. Available at: http://jncimono.oxfordjournals.org/cgi/content/full/2003/31/20. Accessed April 18, 2008.

25. Walboomers JMM, Jacobs MV, Manos MM, Bosch FX, Kummer JA, Shah KV, et al. Human papillomavirus is a necessary cause of invasive cervical cancer worldwide. J Pathol.1999; 189:12 -19.[Medline]

26. The current status of development of prophylactic vaccines against human papillomavirus infection. Geneva, Switzerland: World Health Organization; 1999. Available at: http://www.who.int/vaccines-documents/DocsPDF99/www9914.pdf.

27. Ho GYF, Bierman R, Beardsley L, Chang CJ, Burk RD. Natural history of cervicovaginal papillomavirus infection in young women. N Engl J Med. 1998;338:423-428. Available at: http://content.nejm.org/cgi/content/full/338/7/423. Accessed April 18, 2008.

28. Karlsson R, Jonsson M, Edlund K, Evander M, Gustavsson A, Bodén E, et al. Lifetime number of partners as the only independent risk factor for human papillomavirus infection: a population-based study. Sex Transm Dis. 1995;119 -127.

29. Moscicki AB, Hills N, Shiboski S, Powell K, Jay N, Hanson E, et al. Risks for incident human papillomavirus infection and low-grade squamous intraepithelial lesion development in young females. JAMA. 2001;285:2995-3002. Available at: http://jama.ama-assn.org/cgi/content/full/285/23/2995. Accessed April 18, 2006.

30. 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;290:2070-2076. Available at: http://www.journals.uchicago.edu/doi/full/10.1086/425906. Accessed April 18, 2008.

31. Castellsagué X, Bosch FX, Muñoz N, Meijer CJLM, Shah KV, de Sanjose S, et al. Male circumcision, penile human papillomavirus infection and cervical cancer in female partners. N Engl J Med. 2002;346:1105-1112. Available at: http://content.nejm.org/cgi/content/full/346/15/1105. Accessed April 18, 2008.

32. Castellsagué X, Ghaffari A, Daniel RW, Bosch FX, Muñoz N, Shah KV. Prevalence of penile human papillomavirus DNA in husbands of women with and without cervical neoplasia: a study in Spain and Colombia. J Infect Dis.1997; 176:353 -361.[Medline]

33. Insinga RP, Glass AG, Rush BB. The health care costs of cervical human papillomavirus–related disease. Am J Obstet Gynecol. 2004;191:114 -120.[Medline]

34. Alam M, Stiller M. Direct medical costs for surgical and medical treatment of condylomata acuminata. Arch Dermatol.2001; 137:337 -341.[Abstract/Free Full Text]

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Mayeaux, E. J. PubMed PubMed Citation Articles by Mayeaux, E. J., Jr