- Research article
- Open Access
Upscaling human papillomavirus vaccination in high-income countries: impact assessment based on transmission model
Infectious Agents and Cancer volume 9, Article number: 4 (2014)
The decrease in human papillomavirus (HPV) vaccine prices may allow upscale already started vaccination programmes but the advantages of different options are unclear.
Using a mathematical model of HPV16 and 18 transmission and data on vaccination coverage from Italy, we compared 3 options to upscale an already started programme targeting 11-year old girls (coverage 65%): a) coverage improvement (from 65% to 90%); b) addition of 11-year-old boys (coverage 65%); or c) 1-year catch-up of older girls (coverage 50%).
The reduction of cervical HPV16/18 infection as compared to no vaccination (i.e. effectiveness against HPV16/18) increased from 76% to 98% with coverage improvement in girls and to 90% with the addition of boys. With higher coverage in girls, HPV16/18 infection cumulative probability by age 35 decreased from 25% to 8% with a 38% increase in vaccine number. The addition of boys decreased the cumulative probability to 18% with a 100% increase in the number of vaccinees. For any coverage in girls, the number of vaccinees to prevent 1 woman from being infected by HPV16/18 by age 35 was 1.5, whereas it was 2.7 for the addition of boys. Catch-up of older girls only moved forward the vaccination effectiveness by 2–5 years.
Increasing vaccination coverage among girls is the most effective option for decreasing HPV16/18. If not achievable, vaccinating boys is justifiable if vaccine cost has at least halved, because this option would almost double the number of vaccinees.
The debate on the best target population of human papillomavirus (HPV) vaccination programmes in high-income countries has been renewed by the decision to vaccinate boys in Australia [1, 2] and the similar recommendations from the United States  and by the relevance of non-cervical HPV-related cancers . A key issue is whether an upscale of existing vaccination programmes should aim for increased vaccination of girls and young women or extend vaccination programme to boys . The steady decrease in HPV vaccine prices makes an upscale attractive also for those high-income countries which initially targeted only one or few birth cohorts of girls or achieved low coverage.
The impact of vaccinating adolescent girls (and in some cases also boys) with or without catch-up of older girls has been explored using mathematical models [6–12]. The main aim of these studies was to estimate the incremental cost-effectiveness ratio of different vaccination options . However, cost-effectiveness models are sensitive to the broad variations in the cost of HPV vaccines in different countries and depend on a variety of assumptions regarding incidence, incubation time and incidence rates of the various HPV-associated diseases.
In the present paper, we assess, as an example, different upscaling options in the vaccination programme that started in 2008 in Italy assuming that a fixed amount of resources has been allocated to HPV prevention. Our aim is to compare the effectiveness for HPV infection control of different options for an upscaled vaccination programme, in relation to the effectiveness of the existing baseline programme. We focused on viral endpoints (i.e. HPV16/18 cervical infections), which, though not clinically relevant per se, will be the earliest to be monitored. Three options were explored: a) coverage improvement of initially targeted girls; b) catch-up of a few additional female birth cohorts; and c) the addition of boys.
The transmission dynamic model of HPV infection used in the present paper has been extensively described elsewhere . Briefly, it is a population-based single-type model, which accounts for susceptible, HPV-infected and immune men and women. Each model’s output was fitted to the age-specific (25–29 to 55–59 age group) prevalence curves of cervical HPV16 and 18 infection that were observed in a large (94,370 women) population-based randomized controlled trial of cervical cancer screening (the New Technologies for Cervical Cancer, NTCC, trial) . A total of 100,000 sets of parameter values were generated by independently sampling a uniform distribution for each parameter within a pre-specified range of values . Each set of values was used to generate a model-based age-specific prevalence curve. Finally, the fit of each model’s output to the above-mentioned age-specific prevalence of HPV16 and 18 was assessed by calculating binomial log-likelihood. We selected the 100 model-generated curves that best fitted the observed data and among them we computed, for each parameter, the median and interquartile range (IQR) values as estimates of the most credible parameter values . In order to account for the uncertainty of model-based estimates, the above-mentioned 100 best fitting curves for HPV16 and 18 were used to project the consequences of introducing different vaccination options.
HPV16 and 18 cervical infections were modelled separately as independent infections [16–18]. Clearance of infection was modelled assuming that it would be followed by natural type-specific immune protection in a fraction of women (i.e. 20% and 43%, for HPV16 and 18, respectively). The prevalence of HPV16 and 18 in the observed data was 2.4% and 0.7%, respectively, while 5% of HPV16 and/or HPV18 infected women were co-infected . We eventually reported the impact of vaccination against the combination of the two types (HPV16/18). Vaccine efficacy against HPV16 and 18 infections among women was assumed to be 95% [19, 20]. Vaccine efficacy among men was assumed to be 79% against HPV16 infection , and 95% against HPV18 infection . The base case of an existing vaccination programme was derived from the Italian organized vaccination programme [22, 23], i.e., initial vaccination of 11-year-old girls in 2008 (hereafter referred to as baseline vaccination) and a coverage of 65%  (Figure 1). We assessed the effectiveness of changes in the vaccination programme five years after its inception (2013) using three not mutually exclusive options: a) increasing 11-year-old girls’ coverage to 90% (the target initially set by Italian public health authorities); b) a 1-year catch-up campaign (national coverage assumed as 50%) that targets 17-to-24-year-old women; and c) vaccination of 11-year-old boys, with 65% coverage. As for sensitivity analyses, we repeated the projections increasing up to 65% coverage of catch-up and decreasing the coverage of 11-year-old boys down to 50%.
For each simulated upscale option, we present: 1) the effectiveness of vaccination as a function of calendar year after vaccination; and 2) the percent cumulative probability (CumProb) of HPV16/18 cervical infections by age 35 years according to birth cohort. Effectiveness was defined as the relative reduction in prevalence of HPV16/18 infections in women aged ≤35 years as compared to that in the absence of vaccination. Finally, we directly compared the different vaccination options for a limited number of birth-cohorts by calculating the number of subjects needed to vaccinate (NNV) in order to prevent a woman from being infected by HPV16/18 by age 35. The NNV was calculated assuming that birth cohorts were of the same size and included the same number of boys and girls. The corresponding number of vaccine doses may vary depending on the recommended vaccination schedule.
The improvement of vaccination coverage from 65% to 90% in 11-year-old girls increased the effectiveness against cervical HPV16/18 infections within 30 years since vaccination introduction from 76% to 98% (Figure 2). As a result of herd immunity (i.e. indirect protection of unvaccinated individuals) , effectiveness against HPV16/18 exceeded by 14 and 13 percentage points the one expected if vaccination had only protected vaccinated women (62% effectiveness at 65% coverage and 86% at 90% coverage).
The addition of 11-year-old boys to the vaccination of 11-year-old girls would raise maximal effectiveness to 90%. For both vaccinating boys and increasing coverage, the maximal effectiveness was 99% (Figure 2). The contribution of herd-immunity to vaccination effectiveness was 28 and 14 percentage points, respectively. Lower coverage of boys (i.e. 50%) would result in lower effectiveness.
Catch-up of 17-to-24 year-old women did not affect the long-term effectiveness but it substantially moved it forward compared to baseline vaccination (Figure 3). The anticipation of effectiveness increased, according to a diminishing return pattern, as a function of the number of birth cohorts included in catch-up. For example, catch-up of 17-to-24 year-old young women moved forward mid-maximal effectiveness (38%, i.e., half of the effectiveness expected within 30 years as reported above) against HPV16/18 cervical infections by 2 years. Increasing catch-up coverage to 65% would anticipate effectiveness by about 5 years (data not shown). In no case did vaccination of adolescent boys produce a move forward of programme effectiveness, regardless of girls’ coverage.
Table 1 shows the median and IQR estimates of HPV16/18 CumProb by age 35, by birth cohort and upscale option. In absence of any HPV vaccination, the estimated CumProb was 67.5% (IQR: 56.9 – 75.1). Under the assumption of baseline vaccination of 11-year-old girls, starting with girls born in 1997 and with 65% coverage, CumProb estimates decreased down to 24.9% (IQR: 20.0 – 30.7) among girls belonging to the vaccinated birth cohorts. As the number of birth cohorts vaccinated increased, also the reduction in HPV16/18 CumProb by age 35 slightly increased.
Catch-up of older girls would lower the cumulative probability of HPV16/18 infections among women not initially targeted (Table 1). Targeting 17-to-18-year-old girls would reduce HPV16/18 CumProb by age 35 among 1996-born women to 31.7% (IQR: 25.1 – 38.4), but not among 1993-born women. However, the addition of more than four birth cohorts would not appreciably improve HPV16/18 CumProb (Table 1) because of the large fraction of young women sexually active above age 20.
In absence of catch-up, herd-immunity would also partially protect the last unvaccinated birth cohort (born in 1996), with an expected cumulative probability of HPV16/18 cervical infections of 43.8% (IQR: 35.9 – 51.4). The herd-immunity is expected to be lower among older birth cohorts as a consequence of decrease in sexual mixing with male partners of the vaccinated cohorts. For example, HPV16/18 CumProb among women born in 1993 would overlap the one expected in absence of vaccination (64.9%; IQR: 54.9 – 72.8).
The reduction of HPV16/18 CumProb by age 35 according to a) increase in 11-year-old girls’ coverage to 90%; or b) introduction of vaccination of 11-year-old boys in 2013 is shown in Table 1. Reduction was observed in cohorts born after 1997 in both options. The improvement of 11-year-old girls coverage reduced HPV16/18 CumProb to 8.1% (IQR: 6.0 – 10.2) in 2002-born women. The addition of boys without improving girls’ coverage decreased HPV16/18 CumProb to 17.6% (IQR: 14.1 – 21.5) in the same cohort.
Figure 4 shows the decrease in HPV16/18 CumProb by age 35 among 2002-born women according to different upscale options. Horizontal axis shows the increase in vaccinated individuals relative to 65% coverage of 11-year-old girls only. The improvement of coverage of 11-year-old girls would reduce HPV16/18 CumProb from 25% to 8% and increase vaccinees by 38%. Vaccination of 11-year-old boys (without change in girl coverage) would lead to a reduction in HPV16/18 CumProb from 25% to 18% and increase vaccinees by 100%. Therefore, assuming a fixed amount of resources allocated to the vaccination programme, the improved coverage option would be acceptable if the vaccination cost per capita would be reduced by at least 28%, while the boys’ vaccination option would be acceptable if costs reduction would be at least 50%.
A direct comparison between vaccination options, restricted to the 10 first targeted birth cohorts, showed that the NNV was 1.5 under both the baseline and the improved girls’ coverage option. NNV was 2.7 if boys were also vaccinated (Table 2).
Our results show that improving vaccination coverage in adolescent girls is the most effective upscale option for decreasing the burden of HPV16/18 cervical infections in women. The addition of adolescent boys would approximately double NNV compared to girls’ vaccination but it can be considered useful and cost-neutral if the coverage of girls cannot be further improved and the cost per vaccination has at least halved.
A 1-year catch-up campaign of a few cohorts of older girls and younger women would move forward by about 3-to-5 years the impact of vaccination among targeted cohorts regardless of the vaccination strategy adopted for adolescent girls and boys. However, due to the higher probability of previous exposure to HPV16/18 infection, additional catch-up of older birth-cohorts would follow a diminishing return pattern. The catch-up of young women and improvement of vaccination coverage of 11-year-old adolescents would essentially benefit different birth-cohorts, i.e. those born in 2001 or earlier and after 2001, respectively.
Coverage of 90% of 11-year-old girls would increase the number of vaccinated adolescents by about 40% and decrease to 8% the HPV16/18 CumProb by age 35. The addition of 11-year-old boys with 65% coverage would double the PNN and decrease to 18% HVP16/18 CumProb by age 35 (Figure 4). While the improvement of girls’ coverage is clearly the most cost-effective upscale option (Table 2), the feasibility of achieving the improved coverage is uncertain. For example, a recent study from the US, where less than half of adolescent girls were fully vaccinated, suggested that fostering physician recommendation for vaccination may not be sufficient to increase HPV vaccine uptake in front of increasing families’ concerns about vaccine safety .
However, the cost of coverage improvement varies by setting, e.g., more expensive in on-demand programmes than in school- and/or by population-based invitations.
In Italy, for instance, vaccination against hepatitis B virus included catch-up of 12-year-old adolescents in ad hoc public clinics by active invitation between 1991 and 2003. Adolescent coverage reached 90% in most Italian regions . Many conditions have, however, changed in the last decades including the current voluntariness of vaccinations, population’s attitude towards vaccines, and, in the case of HPV vaccination, the existence of screening as an alternative approach to cervical cancer prevention .
Our study shows that the different vaccination options also provide indirect protection against HPV16/18 to unvaccinated women. This indirect protection results from the decline in HPV transmission in sexual network that includes a high proportion of vaccinated women. Vaccinated women can indirectly protect the unvaccinated women by sharing sexual partners, while vaccinated boys directly prevent the transmission of HPV16/18 to unvaccinated women.
Our study has strengths and limitations. We focused on viral endpoints, although these are not clinically relevant outcomes, as they represent the earliest possible endpoints for monitoring vaccination programmes and the accuracy of model-based projections. We concentrated on HPV16/18 infections as information about natural history and vaccine cross-protection against other high-risk HPV types is limited. Restriction to virological endpoints up to age 35 minimizes the potential impact of different cervical screening practice on the interpretation of our findings . Furthermore, we avoided the uncertainties inherent in estimating the cost and quality of life associated with the various HPV-associated diseases in men and women.
The generalizability of estimates based on dynamic model projection is largely dependent on the quality of assumptions of the parameters that govern natural history and sexual circulation of HPV infection. To test the validity of our sets of parameter values, we independently calibrated our Italian data-based model to Swedish data. Allowing for demographic and behavioural differences between the two countries and populations, the sets of parameters that regulate the natural history of HPV16 and 18 infections were shown to be consistent, suggesting that our projections are robust . By contrast, our estimates, in particular for catch-up, are unlikely to satisfactorily apply to countries with significantly different patterns of sexual behaviours of adolescents and young women. Effectiveness of catch-up in our model was influenced by the Italian vaccination programme, in which HPV vaccination had been nearly restricted to 11-year-old girls for the first 5 years. Our findings, therefore, may be of particular interest for programmes with a similar initial set up. By contrast, the comparison of improving coverage of adolescent girls and/or vaccinating also boys is of interest to most high-income countries.
Our study only included estimates of vaccination benefit in women, although the reduction in incidence of HPV infection and HPV-associated cancers in men is an additional benefit of vaccination . However, much fewer studies have addressed the natural history of HPV infections among men than women  and existing data are still insufficient to accurately calibrate a dynamic model that will allow reliable projections for males.
Due to the rapidly changing price of HPV vaccination, we chose not to include the monetary costs of purchasing and delivering HPV vaccines. However, the percent increase in vaccinated individuals in each vaccination option, as well as the NNV to prevent one woman HPV16 or 18 infected by age 35 should be easily applicable to Country-specific vaccination costs in any given year and recommended number of vaccine doses . NNV according to different options is especially useful as a guide to cost-effectiveness. If NNV doubles, as it is the case for boys, an upscale will be cost-neutral if vaccine cost had at least halved.
Number needed to vaccinate
New technologies for cervical cancer.
Salisbury DM: Male vaccination against human papillomavirus. Lancet Infect Dis. 2012, 12: 582-583. 10.1016/S1473-3099(12)70082-8.
Donovan B, Franklin N, Guy R, Grulich AE, Regan DG, Ali H, Wand H, Fairley CK: Quadrivalent human papillomavirus vaccination and trends in genital warts in Australia: analysis of national sentinel surveillance data. Lancet Infect Dis. 2011, 11: 39-44. 10.1016/S1473-3099(10)70225-5.
Centers for Disease Control and Prevention (CDC): Recommendations on the use of quadrivalent human papillomavirus vaccine in males--Advisory Committee on Immunization Practices (ACIP). MMWR Morb Mortal Wkly Rep. 2011, 60: 1705-8.
Forman D, de Martel C, Lacey CJ, Soerjomataram I, Lortet-Tieulent J, Bruni L, Vignat J, Ferlay J, Bray F, Plummer M, Franceschi S: Global burden of human papillomavirus and related diseases. Vaccine. 2012, 30: F12-F23.
Georgousakis M, Jayasinghe S, Brotherton J, Gilroy N, Chiu C, Macartney K: Population-wide vaccination against human papillomavirus in adolescent boys: Australia as a case study. Lancet Infect Dis. 2012, 12: 627-634. 10.1016/S1473-3099(12)70031-2.
French KM, Barnabas RV, Lehtinen M, Kontula O, Pukkala E, Dillner J, Garnett GP: Strategies for the introduction of human papillomavirus vaccination: modelling the optimum age- and sex-specific pattern of vaccination in Finland. Br J Cancer. 2007, 96: 514-518. 10.1038/sj.bjc.6603575.
Kim JJ, Goldie SJ: Health and economic implications of HPV vaccination in the United States. N Engl J Med. 2008, 359: 821-832. 10.1056/NEJMsa0707052.
Jit M, Choi YH, Edmunds WJ: Economic evaluation of human papillomavirus vaccination in the United Kingdom. BMJ. 2008, 337: a769-10.1136/bmj.a769.
Bogaards JA, Coupe VM, Meijer CJ, Berkhof J: The clinical benefit and cost-effectiveness of human papillomavirus vaccination for adult women in the Netherlands. Vaccine. 2011, 29: 8929-8936. 10.1016/j.vaccine.2011.09.055.
Chesson HW, Ekwueme DU, Saraiya M, Dunne EF, Markowitz LE: The cost-effectiveness of male HPV vaccination in the United States. Vaccine. 2011, 29: 8443-8450. 10.1016/j.vaccine.2011.07.096.
Elbasha EH, Dasbach EJ: Impact of vaccinating boys and men against HPV in the United States. Vaccine. 2010, 28: 6858-6867. 10.1016/j.vaccine.2010.08.030.
Regan DG, Philp DJ, Hocking JS, Law MG: Modelling the population-level impact of vaccination on the transmission of human papillomavirus type 16 in Australia. Sex Health. 2007, 4: 147-163. 10.1071/SH07042.
Baussano I, Elfstrom KM, Lazzarato F, Gillio-Tos A, De Marco L, Carozzi F, Del Mistro A, Dillner J, Franceschi S, Ronco G: Type-Specific Human Papillomavirus Biological Features: Validated Model-Based Estimates. 2013, e81171-8
Ronco G, Giorgi-Rossi P, Carozzi F, Confortini M, Dalla Palma P, Del Mistro A, Ghiringhello B, Girlando S, Gillio-Tos A, De Marco L, Naldoni C, Pierotti P, Rizzolo R, Schincaglia P, Zorzi M, Zappa M, Segnan N, Cuzick J, New Technologies for Cervical Cancer screening (NTCC) Working Group: Efficacy of human papillomavirus testing for the detection of invasive cervical cancers and cervical intraepithelial neoplasia: a randomised controlled trial. Lancet Oncol. 2010, 11: 249-257. 10.1016/S1470-2045(09)70360-2.
Hoare A, Regan DG, Wilson DP: Sampling and sensitivity analyses tools (SaSAT) for computational modelling. Theor Biol Med Model. 2008, 5: 4-10.1186/1742-4682-5-4.
Vaccarella S, Franceschi S, Snijders PJ, Herrero R, Meijer CJ, Plummer M: Concurrent infection with multiple human papillomavirus types: pooled analysis of the IARC HPV prevalence surveys. Cancer Epidemiol Biomarkers Prev. 2010, 19: 503-510. 10.1158/1055-9965.EPI-09-0983.
Carozzi F, Ronco G, Gillio-Tos A, De Marco L, Del Mistro A, Girlando S, Franceschi S, Plummer M, Vaccarella S, New Technologies for Cervical Cancer screening (NTCC) Working Group: Concurrent infections with multiple human papillomavirus (HPV) types in the New Technologies for Cervical Cancer (NTCC) screening study. Eur J Cancer. 2012, 48: 1633-1637. 10.1016/j.ejca.2011.10.010.
Vaccarella S, Franceschi S, Herrero R, Schiffman M, Rodriguez AC, Hildesheim A, Burk RD, Plummer M: Clustering of multiple human papillomavirus infections in women from a population-based study in Guanacaste, Costa Rica. J Infect Dis. 2011, 204: 385-390. 10.1093/infdis/jir286.
Paavonen J, Naud P, Salmeron J, Wheeler CM, Chow SN, Apter D, Kitchener H, Castellsague X, Teixeira JC, Skinner SR, Hedrick J, Jaisamrarn U, Limson G, Garland S, Szarewski A, Romanowski B, Aoki FY, Schwarz TF, Poppe WA, Bosch FX, Jenkins D, Hardt K, Zahaf T, Descamps D, Struyf F, Lehtinen M, Dubin G, HPV PATRICIA Study Group: Efficacy of human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine against cervical infection and precancer caused by oncogenic HPV types (PATRICIA): final analysis of a double-blind, randomised study in young women. Lancet. 2009, 374: 301-314. 10.1016/S0140-6736(09)61248-4.
Wheeler CM, Kjaer SK, Sigurdsson K, Iversen OE, Hernandez-Avila M, Perez G, Brown DR, Koutsky LA, Tay EH, García P, Ault KA, Garland SM, Leodolter S, Olsson SE, Tang GW, Ferris DG, Paavonen J, Steben M, Bosch FX, Dillner J, Joura EA, Kurman RJ, Majewski S, Muñoz N, Myers ER, Villa LL, Taddeo FJ, Roberts C, Tadesse A, Bryan J: The impact of Quadrivalent Human Papillomavirus (HPV; Types 6, 11, 16, and 18) L1 virus-like particle vaccine on infection and disease due to oncogenic nonvaccine hpv types in sexually active women aged 16–26 years. J Infect Dis. 2009, 199: 936-944. 10.1086/597309.
Giuliano AR, Palefsky JM, Goldstone S, Moreira ED, Penny ME, Aranda C, Vardas E, Moi H, Jessen H, Hillman R, Chang YH, Ferris D, Rouleau D, Bryan J, Marshall JB, Vuocolo S, Barr E, Radley D, Haupt RM, Guris D: Efficacy of quadrivalent HPV vaccine against HPV infection and disease in males. N Engl J Med. 2011, 364: 401-411. 10.1056/NEJMoa0909537.
Giambi C: Tassi di copertura vaccinale per HPV in Italia. IJPH. 2011, Vol 8, Num 3 (suppl 1): S23-27.http://www.ijph.it/pdf/56/023.pdf,
Dorleans F, Giambi C, Dematte L, Cotter S, Stefanoff P, Mereckiene J, O’Flanagan D, Lopalco PL, D’Ancona F, Levy-Bruhl D, Dorleans F, Giambi C, Dematte L, Cotter S, Stefanoff P, Mereckiene J, O’Flanagan D, Lopalco PL, D’Ancona F, Levy-Bruhl D, VENICE 2 project gatekeepers group: The current state of introduction of human papillomavirus vaccination into national immunisation schedules in Europe: first results of the VENICE2 2010 survey. Euro Surveill. 2010, 15 (47): Available from: URL: http://www.eurosurveillance.org/
Giambi C: Stato di avanzamento della campagna vaccinale per l’HPV: dati di copertura vaccinale al 31/12/2010 eaggiornamento delle decisioni in merito alle strategie vaccinali. Istituto Superiore di Sanità: Reparto di Epidemiologia di Malattie Infettive del CNESPS,http://www.epicentro.iss.it/,
Garnett GP: Role of herd immunity in determining the effect of vaccines against sexually transmitted disease. J Infect Dis. 2005, 191 (Suppl 1): S97-106.
Darden PM, Thompson DM, Roberts JR, Hale JJ, Pope C, Naifeh M, Jacobson RM: Reasons for not vaccinating adolescents: National Immunization Survey of Teens, 2008–2010. Pediatrics. 2013, 131: 645-651. 10.1542/peds.2012-2384.
Bonanni P, Pesavento G, Bechini A, Tiscione E, Mannelli F, Benucci C, Nostro AL: Impact of universal vaccination programmes on the epidemiology of hepatitis B: 10 years of experience in Italy. Vaccine. 2003, 21: 685-691. 10.1016/S0264-410X(02)00580-7.
Kane MA: Preventing cancer with vaccines: progress in the global control of cancer. Cancer Prev Res (Phila). 2012, 5: 24-29. 10.1158/1940-6207.CAPR-11-0533.
Schiffman M, Castle PE, Jeronimo J, Rodriguez AC, Wacholder S: Human papillomavirus and cervical cancer. Lancet. 2007, 370: 890-907. 10.1016/S0140-6736(07)61416-0.
Michels KB, Zur Hausen H: HPV vaccine for all. Lancet. 2009, 374: 268-270. 10.1016/S0140-6736(09)61247-2.
Giuliano AR, Lee JH, Fulp W, Villa LL, Lazcano E, Papenfuss MR, Abrahamsen M, Salmeron J, Anic GM, Rollison DE, Smith D: Incidence and clearance of genital human papillomavirus infection in men (HIM): a cohort study. Lancet. 2011, 377: 932-940. 10.1016/S0140-6736(10)62342-2.
Kreimer AR, Rodriguez AC, Hildesheim A, Herrero R, Porras C, Schiffman M, González P, Solomon D, Jiménez S, Schiller JT, Lowy DR, Quint W, Sherman ME, Schussler J, Wacholder S, CVT Vaccine Group: Proof-of-principle evaluation of the efficacy of fewer than three doses of a bivalent HPV16/18 vaccine. J Natl Cancer Inst. 2011, 103: 1444-1451. 10.1093/jnci/djr319.
The research leading to these results has received funding from the European Community’s Seventh Framework programme (FP7/2007-2013) under grant agreement No. 242061 (acronym PREHDICT) and from the European Commission's Seventh Framework programme (FP7/2007-2013) under grant agreement No. 603019 (acronym CoheaHr). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
IB, FL, GR, SF declare that they have no competing interests. JD has acted as consultant and received research grants from Merck and SPMSD.
IB, JD, GR and SF conceived and designed the study. IB and FL conceived, coded, and ran the transmission model. IB performed the analyses. GR and JD contributed to literature search, data collection and findings interpretation. IB and SF wrote the manuscript. All authors approved the final manuscript.