Estimating long-term clinical effectiveness and cost-effectiveness of HPV 16/18 vaccine in China
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Human papillomavirus (HPV) 16 and 18 are the two most common HPV oncogenic types that can be prevented by vaccination. This study aimed at assessing the cost-effectiveness of 3 doses of the bivalent HPV vaccine in rural and urban settings in China.
A Markov model was adapted to reflect the lifetime of a modelled 100,000 12-year-old girls cohort in rural and urban settings in China. Input parameters were obtained from published literature, official reports and a two-round expert review panel. Clinical and economic outcomes of vaccination at age 12 with screening was compared to screening only. In the base case analysis, a 3 % discount rate, the vaccine cost of 247 CNY (US$ 39, PAHO vaccine cost in 2013), two rounds of screening in a life time and 70 % coverage for both screening and vaccination were used. One-way, two-way and probabilistic sensitivity analyses were performed. We used different thresholds of cost-effectiveness to reflect the diversity of economic development in China.
Vaccination in addition to screening could prevent 60 % more cervical cancer cases and deaths than screening only. The incremental cost effectiveness ratio varied largely when changing cost of vaccination and discount in one way analysis. Vaccination was very cost-effective when the vaccine cost ranged 87-630 CNY (US$ 13.8-100) in rural and 87-750 CNY (US$ 13.8–119) in urban; and remained cost-effective when the vaccine cost ranged 630–1,700 CNY (US$ 100–270) in rural and 750–1,900 CNY (US$ 119–302) in urban in two way analysis. Probabilistic sensitivity analyses showed that model results were robust.
In both rural and urban, the vaccination cost and discounting are important factors determining the cost-effectiveness of HPV vaccination; policy makers in China should take these into account when making a decision on the introduction of HPV vaccine. In areas with a high burden of cervical cancer and limited screening activities, HPV vaccination should be prioritized. However, the vaccine cost needs to be reduced in order to make it very cost-effective and affordable as well, in particular in poverty areas with high disease burden.
KeywordsCervical cancer HPV vaccine Cost-effectiveness
3 Doses of Bivalent HPV Vaccination
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Cervical Intraepithelial Neoplasia
Expanded Programme on Immunisation
Global Alliance for Vaccines and Immunization
Gross Domestic Product
Incremental Cost-effectiveness Ratio
Not included in probabilistic sensitivity analyses
Pan American Health Organization
PApilloma TRIal against Cancer In young Adults
Probabilistic Sensitivity Analyses
United States Dollar
Visual Inspection with Acetic Acid/Lugol’s Iodine
World Health Organization
Given its large population, China accounted for 11.7 % of the world’s cervical cancer (CC) cases and 11.3 % of the world’s CC deaths in 2012 . Since 2009, a screening programme has been implemented in rural China targeting women aged 35 to 64 years, which has gradually expanded from screening 10 million women over a period of 3 years to screening 10 million women per year. Women in urban areas have access to CC screening on an opportunistic basis or through their employment. However, the mortality was reported to increase at an annual rate of 4.1% in young urban women aged 35 to 44 . Furthermore, there are also wide disparities in CC incidence, mortality and screening accessibility between rural and urban areas in China .
Persistent HPV infection is the main cause of CC . Seventy percent of all CC worldwide is caused by HPV 16/18 ; in China, HPV 16/18 infection accounts for 84.5 % of squamous cell carcinoma . Prophylactic HPV vaccines may add to current efforts of screening in reducing CC burden in China. There are currently two vaccines available globally: a bivalent vaccine produced by GSK (Cervarix®) and a quadrivalent vaccine produced by Merck (Gardasil®). Both vaccines protect against HPV types 16 and 18 while the quadrivalent vaccine also protects against non-oncogenic types 6 and 11. Cervarix®, a bivalent vaccine (GSK, Wavre, Belgium) has been widely used in over 100 countries through regional or national immunization programs to prevent HPV 16/18 infection and related diseases. Cervarix® has shown high immunogenicity and safety, and induces a high degree of protection against HPV-16/18 infection and associated cervical lesions [7, 8]. To date, only Cervarix® has just been approved by Chinese Food and Drug Administration in July 2016 after completation of phase III clinical trials using 3 doses of bivalent HPV vaccination (3DBV) in mainland China [9, 10].
Because the HPV vaccine is relatively costly , it has been subject to careful scrutiny. With the increasing importance of economic evaluation in priority setting for health , the cost-effectiveness of vaccination strategies should be considered before inclusion in national programmes, as recommended by the World Health Organization (WHO) position paper on HPV vaccines . Mathematical models can help to estimate the long term effectiveness of HPV vaccination in parallel to clinical trials. Such models use a simplified description of the natural history leading to cervical cancer and provide a formal framework to synthesize information from various sources . Modelling studies can integrate currently available clinical data with country-specific epidemiological data to evaluate the potential long-term impact of adding vaccination to screening .
Given the important resource implications of introducing the HPV vaccine in China, the financing of the HPV vaccination programme needs to be carefully considered to ensure the best use of resources compared to other priorities in China [16, 17, 18]. To date, there have been few comprehensive analyses evaluating the long-term impact of the HPV vaccine in China [19, 20]. Furthermore China is characterized by substantial differences in economic development and disease distribution between regions and therefore the diversity of economic, the ability to pay and screening influence should be considered to achieve the health care fairness. In such context, it is important to advance equity in China’s health system if implementing HPV vaccination in national vaccination program. We aimed to estimate the cost-effectiveness of HPV vaccination using Chinese specific parameters.
This study was approved by the Human Subjects Review Boards (Approval No. 13-066/742) of the Cancer Institute and Hospital, Chinese Academy of Medical Sciences (CICAMS). We used a Markov model developed in Microsoft Excel to evaluate the long-term clinical effectiveness and cost-effectiveness of the bivalent vaccine in both rural and urban China for a hypothetical cohort of 100,000 12-year-old girls (Additional file 1: Figure S1).
The Markov model was adapted from previously published models by Debicki  and Konno  and has been used to perform cost-effectiveness analyses in other countries such as Canada, Taiwan and Japan. The model simulated the natural history of cervical cancer (extending from infection to death) in the hypothetical cohort of 12-year-old girls who are vaccinated in addition to current screening or screening only for cervical cancer, with follow up for a life-time. The Markov model has a cycle time of 1 year and run over life-time of the cohort according to the mortality rate for women reported by National Bureau of Statistics of China . Study parameters were obtained through expert review, literature review and data extraction from previous studies. The study did not collect information from patients and informed consent was therefore not needed. A 3 % discount rate was used with a range (0–5 %) for sensitivity analysis according to the WHO guidelines . The same discount rates for health outcomes and costs were used.
Globally, cervical cancer is considered an important public health problem and disease burden could be reduced by HPV vaccines. In developing countries, the main challenge for the introduction of the HPV vaccine is its price. Evidence from Mexico, Panama and other developing countries showed high vaccination coverage when including HPV vaccine in the national immunization programs by government . Based on the successful experience of hepatitis B vaccine in China, we assumed the government would strengthen the vaccination of HPV according to the China National Plan for NCD Prevention and Treatment . We expect our cost-effectiveness modelling analysis could benefit the health policy, especially public health policy decisions and budget-impact. Based on the considerations above, we chose the health care payer perspective  and considered only direct medical costs.
Base case analysis
The base case analysis was conducted for a hypothetical cohort of 100,000 12-year-old girls. We considered two scenarios: HPV vaccination in addition to screening against screening only, separately for rural and urban areas. The cost-effectiveness of HPV vaccination was evaluated by comparing the two scenarios.
The screening and treatment costs were collected by a micro-costing approach  from previous studies [30, 31] to estimate aggregated costs associated with cervical cancer, and re-evaluated by a two round expert review panel. Since most patients in China with diagnostically confirmed CC seek treatment in urban hospitals, only the treatment cost of CC in urban areas was estimated. Costs were calculated in Chinese Yuan (CNY), and converted to US dollars (US$) at an exchange rate of 1 US$ = 6.3 CNY for 2013. The two round expert panel lasted for five months. Eight rural and twelve urban clinical gynecologists, epidemiologists and economists chosen from Northern (Beijing, Tianjin, Liaoning), Central (Henan, Shanxi, Jiangsu), Western (Xinjiang) and Southwestern (Sichuan) of China were selected to evaluate the costs of screening, costs of treatment and the proportions of women receiving or refusing the treatment procedures for cancer patients .
China is not a member of the Global Alliance for Vaccines and Immunization (GAVI) or the Pan American Health Organization (PAHO) [33, 34], but we assumed China could likely negotiate lower public sector prices . Since China’s GDP per capita is similar to most PAHO countries, such as Peru, Brazil and Chile [34, 36], we assumed in the base case analysis a vaccine cost similar to the PAHO cost (247 CNY (US$ 39) in 2013). In addition, since HPV vaccine price has not been available in China, we obtained the unit cost of vaccine administration from a previous publication on hepatitis B vaccination . We assumed that the HPV vaccine would be delivered through the expanded programme on immunisation (EPI) and would rely on the existing management system (personnel, equipment, cold chain etc.). We therefore only considered the incremental cost of adding the HPV vaccine to the EPI programme, and included the cost of salaries, surveillance, propaganda, training, supervision, transportation, cold chain and other equipments that were related to vaccine delivery. The incremental vaccine administration cost for an additional dose of hepatitis B vaccine was 18 CNY (US$ 3) per child per dose  and therefore 54 CNY (US$ 9) for 3-doses of the HPV vaccine. The administration cost was assumed to be the same in rural and urban settings, since our analysis was under the scenario of government supported national vaccination program based on the experience of the hepatitis B vaccine.
The utilities in our model have been used in previously published studies [38, 39, 40, 41, 42]. The model assumed no decrements in utility from competing morbidities for non-infected, non-disease-stage subjects. The data of transition probabilities were calculated from the CICAMS pooled database which included more than 30,000 women across China of 17 population-based studies in 9 provinces (Shanxi, Beijing, Henan, Jiangxi, Xinjiang, Shanghai, Jiangsu, Gansu and Guangdong) , expert panel and derived from the literature [44, 45, 46, 47, 48]. In general, HPV infection increases in young women after sexual debut, but a majority proportion of the HPV infection among young female clears on its own. The HPV incidences were calculated from the CICAMS database . We assumed the age of first sexual debut at 15-year-old in Chinese girls (and therefore assumed no HPV infection in girls under the age of 15 years). The CICAMS database showed that HPV incidence increased from 15-year-old to 25-year-old and decreased from 25-year-old to 40-year-old, then increased again from 40 to 60-year-old .
The vaccine efficacy parameters varied with different degrees of cervical intraepithelial neoplasia (CIN1, CIN2 and CIN3). A 93.2 % overall vaccine efficacy against CC irrespective of types, 64.9 % efficacy against CIN2/3 irrespective of types and 50.3 % against CIN1 irrespective of types were assumed in the model . The vaccine coverage was assumed at 70 % both in rural and urban according to the hepatitis B vaccination uptake after 3 years on the market.
The 70 % screening coverage was obtained from cross-sectional studies in China [50, 51]. Screening in rural areas is currently done using Pap smear or visual inspection with acetic acid/Lugol’s iodine (VIA/VILI) [52, 53], while in urban areas Pap smear is the only used primary screening method according to the survey and the expert review panel [32, 54]. The screening sensitivities for CIN1 and CIN2/3 were calculated from the CICAMS database . Both screening scenarios assumed in a lifetime screening at ages 35 and 45, according to cervical cancer screening guidelines for developing countries .
The main outcome measure used in the model was the ICER (Incremental Cost-effectiveness Ratio = Incremental Cost per Quality-adjusted Life-years (QALYs)). As there are substantial differences in economic development between rural and urban China, and there is no data on GDPs for rural and urban areas separately, the cost-effectiveness threshold should be considered carefully. We evaluated the cost-effectiveness results against 2 different thresholds in the base case analysis: the intervention was considered very cost-effective if the ICER was less than one time the country’s GDP (i.e., 41,908 CNY, US$ 6,652) and cost-effective if the ICER was less than three times the country’s GDP (i.e., 125,723 CNY, US$ 19,956) [55, 56]. Other measures including the number of cervical cancer cases prevented, deaths avoided, and average life-years and QALY gained for one age cohort were studied over lifetime. In addition, accumulated cost and QALY gained per woman, plus the ICER of 3DBV programme versus screening were calculated. The main input parameters are shown in Additional file 2: Table S1.
One-way sensitivity analysis
One-way sensitivity analysis was performed to account for methodological, structural and parameter uncertainties and assumptions. The changes of values used were listed in Additional file 2: Table S1. In one-way sensitivity analysis, one parameter would be changed in a certain range while other parameters were kept constant. Most parameters were varied by +/- 20 % from the base case, with the exception of the vaccine cost. The vaccine cost (for 3 doses) was varied from a minimum of 87 CNY (US$ 13.8) which is the GAVI cost to 1,900 CNY (US$ 302) which is the Hong Kong listed private sector cost [33, 34]. Other parameters that were examined in the sensitivity analysis included the discount rate (0/5 %), vaccine efficacy (95 % confidence interval, 95 % CI), screening age (-/+ 5 years) and the vaccination age (12/18 years).
Two-way sensitivity analysis
Two-way sensitivity analysis was conducted by varying both the vaccine cost from 87 CNY (US$ 13.8) to 1,900 CNY (US$ 302) per course and another parameter, either the discount rate (0/5 %), CC mortality (+/- 20 % from the base case), or screening coverage (30/50 % screening coverage). These three parameters were included in the two-way sensitivity analysis for the following reasons: the discount rate has been shown to be an important parameter that may affect cost-effectiveness results; the CC mortality may vary across different regions of China and the screening coverage can be improved with adequate resources and may therefore change over time. According to base case, which using three times national GDP as the threshold of cost-effectiveness and one time national GDP as the threshold of very cost-effectiveness, the two-way sensitivity analysis would also be conducted in the two thresholds. In addition, taking into account the tremendous varieties of China’s current screening coverage in all regions, screening coverage evaluation were paid specially attention in the analyses. As 70 % screening coverage were extracted from well-designed research studies, we set 70 % as the base case screening coverage but for the current screening status, the screening coverage would be extremely low (6.25 % in rural and 21.5 % in urban). As a result, a lower screening coverage (30 and 50 %) would be analysed in two way price threshold sensitivity analyses and 70 % were assumed to be the idealized screening coverage.
Probabilistic sensitivity analysis (PSA)
In the PSA, all the main input parameters were changed for each calculation. The combined effect of variations in model inputs were explored via multivariate PSA using @Risk® software (Palisade Corporation) in the Excel model. Distributional functions were assigned to each variable for probabilistic sensitivity analysis to evaluate the robustness of the results.
In PSA, the input distributions were set to be normal distributions (limited between 0 and 1 for transition probabilities) when 95 % CI and Standard Deviations (SD) were available. Otherwise, the uniform distribution with a variation +/- 20 % was used when there were no mean, SD or ranges available (Additional file 2: Table S1). In total, 10,000 samples were generated from the assigned distribution.
Base case cost-effectiveness results without discounting and with discount rate 3 % for both costs and benefits
Screening only (A)
Screening + vaccination (B)
ICER (CNY per QALY gained)
ICER (US$ per QALY gained)
Screening only (A)
Screening + vaccination (B)
ICER (CNY per QALY gained)
ICER (US$ per QALY gained)
Under the circumstance that girls were regularly screened twice in their life time, considering the 3 % discount rate, 70 % screening and vaccination coverage and PAHO cost, HPV vaccination had an ICER of 11,365 CNY (US$ 1804) in rural and 6124 CNY (US$ 972) in urban, which is much lower than the national GDP 2013 (41,908 CNY, US$ 6652), which meant that HPV vaccination was very cost effective in this context.
For rural setting, when comparing vaccination in addition to screening with screening only, with 3 % discount, 95.8 % of the replicates predicted to have greater lifetime costs and greater QALY benefit than the screening only scenario (Quadrant I of Fig. 4a). 4.2 % of dots fell into Quadrant II meant that vaccine combined with screening would cost less but gained more QALYs than screening only (Quadrant II in Fig. 4a). When undiscounted, 10.2 % of the replicates predicted to have greater lifetime costs and greater QALY benefit than the screening only in rural (Quadrant I of Fig. 4b). 89.8 % of dots fell into Quadrant II meant that vaccine combined with screening would cost less but gained more QALYs than screening only (Quadrant II in Fig. 4b). For urban setting, when comparing vaccination in addition to screening with screening only, with 3 % discount, 75.5 % of the replicates predicted to have greater lifetime costs and greater QALY benefit than the screening only scenario (Quadrant I of Fig. 4c). 24.5 % of dots fell into Quadrant II meant that vaccine combined with screening would cost less but gained more QALYs than screening only (Quadrant II in Fig. 4c). When undiscounted, 0.5 % of the replicates predicted to have greater lifetime costs and greater QALY benefit than the screening only in urban (Quadrant I of Fig. 4d). 99.5 % of dots fell into Quadrant II meant that vaccine combined with screening would cost less but gained more QALYs than screening only (Quadrant II in Fig. 4d).
The results showed that most of the replicates were in Quadrant I with 3 % discount and Quadrant II with 0 % discount, showing that vaccination in addition to screening had greater QALY benefit compared to screening only. All the replicates were less than the threshold of 3 times national GDP, that represented 100 % of replicates were cost-effectiveness in rural and urban respectively.
The ongoing screening programme with conventional Pap smear or visual inspection will inevitably miss many pre-cancer lesions due to the limitations of these two methods and the lack of health care workers . Moreover, almost ten years delay of the HPV vaccine in China would cause more than 59 million Chinese girls aged 9-15 to lose their opportunities for vaccination  and put 206,000 girls at high risk for cervical cancer over the next 25 years . HPV vaccine may add to current efforts of screening in reducing cervical cancer burden in China in the future.
In the current screening programme, considering the different situation in rural and urban areas, our study analysed two screening strategies respectively to reflect the difference in screening practice between rural and urban settings. Input parameters for rural and urban differed by HPV incidence, proportion of precancers treated, screening and treatment costs for precancerous lesions. The vaccine coverage was assumed the same (70 %) in rural and urban based on the perspective that government would include HPV vaccine in the national vaccination program as well as the success experiences of Hepatitis B vaccine in China. We also set the same methods for cancer treatment between rural and urban, given the realistic situation that most of the rural patients with diagnostically confirmed cervical cancer would seek for treatment in the urban hospitals due to no cancer therapeutic capacity in rural areas. The administration cost was US$ 9 per course, which was similar to previous published studies [18, 60]. The main findings showed that vaccination with 70 % coverage of 3DBV in 12-year-old girls in addition to screening could prevent 60 % more cervical cancer cases and deaths than screening only in China. In a case-control study in United States , the prevalence of HPV16/18 in CIN2+ lesions was demonstrated to decrease from 53.6 to 28.4 % among women received at least one dose of HPV vaccine (P trend < 0.001), which could lead to the reduction of cervical cancer in the future.
The perspective of health care payer was used in this study. Compared with societal perspective which considered the patient time, travel costs, willingness-to-pay and many other indirect parameters, the health care payer perspective could provide more information for the informing budget impact and policy decisions. As decisions on introduction of vaccines are often influenced by funding agencies, analysis such as budget impact assessments focusing on cost-saving, affordability and sustainability are relevant in resource-constrained settings [18, 62, 63]. The costs borne by providers (e.g., donors and governments) which separated by patients and their families could allow judgments to be made from the viewpoints of the various decision-makers. This is particularly important for middle and low income countries that may be required to fully-finance the cost of vaccines. Lieu  estimated (based on existing knowledge about the vaccine at the time) that from the health care payer perspective pneumococcal vaccination of healthy infants in the United States would result in savings if the vaccine cost US$ 18 or less per dose, but from the societal perspective, the vaccination programme would result in savings if the vaccine cost US$ 46 or less per dose. Analysts should therefore be cognizant that whilst a broader perspective that includes productivity losses (gains) will improve cost-effectiveness, it can also be used to justify higher vaccine cost, as it increases the break-even price per dose, i.e., the price at which the cost of the vaccination programme is exactly off-set by the savings due to vaccination .
In the sensitivity analysis, whether the results were cost-effective or not depended on the variability of the key input parameters. HPV vaccination was very cost-effective if the price was lower than 630 CNY (US$ 100) in rural and 750 CNY (US$ 119) in urban in two-way analysis. In order to be very cost-effective, the vaccine cost should be reduced in areas with lower cervical cancer mortality and higher screening coverage. Health care payers should compare the economic development level with the national threshold, CC mortality, HPV infection, HPV genotypes distribution, screening coverage, screening methods and other dominant parameters to decide the appropriate vaccination price. Global cost-effectiveness analysis informed by country-based evidence suggests that vaccinating pre-adolescent girls can be cost-effective, particularly in resource-constrained settings where alternative cervical cancer prevention and control measures often have limited coverage [66, 67, 68, 69]. In the base case, we assumed the screening coverage as 70 % according to the previous research studies in China [50, 51], the coverage rate in real world setting would be much lower, for an instance, it was only 21.5 % in urban  and 6.25 %  in rural so far. For areas with low screening coverage and high cervical cancer burden, HPV vaccination could be more cost-effective and more urgent to be included into the vaccination plans.
Due to the diverse economic development of China, the different areas have different affordability profile. Since 2008, Panama has been the first country in Latin America and the Caribbean to provide the HPV vaccine free of charge to young adolescent girls . After that, many developing countries have implemented the HPV vaccine [71, 72] into national programmes. In China, the government would strengthen the vaccination of HPV according to the China National Plan for NCD Prevention and Treatment . However, the vaccine coverage and price would be the critical factors to be considered in the planning of vaccination programme.
In order to promote the implementation of HPV vaccine in China, multiple surveys have been done to gauge HPV vaccine awareness and knowledge. These multi-centre surveys in China showed that there was a high acceptability of HPV vaccine to prevent CC among Chinese women, but the price paid by individual should be considered carefully when the vaccines become available [73, 74]. The vaccine safety and efficacy would be the main concerns of HPV vaccine among Chinese . Further proof of vaccine safety and efficacy and government subsidies combined with increased awareness could facilitate development and implementation of HPV vaccination in China.
Our analyses assumed the cost of 3 doses of HPV vaccine considering the registration clinical trial in China is for 3-dose vaccine regime. While the WHO position paper  on HPV vaccines proposed that the adoption of a 2-dose vaccine schedule could be recommended for girls aged 9–13 years. A 2-dose vaccine schedule might be more cost-effectiveness due to the non-inferior efficacy and less cost compared to 3-dose schedule.
Not only one-way sensitivity analysis, but also two-way analysis and probabilistic analysis were performed to certify the stability of the model. The main findings in our study were consistent with the previous published studies that evaluate the cost-effectiveness of HPV vaccination in China [19, 20]. We all found that combined HPV vaccination with screening would be more cost-effectiveness than only screening under a certain vaccine cost. The results in our study showed that adding vaccination to screening would reduce 60 % more cancer, while the other study showed a 44 % cancer reduction . And the discrepancies between our study and others mainly occurred in the input parameters. The parameters in our Markov model were collected by multiple channels and validated by the expert panel, in which the experts came from different regions to fully capture the heterogeneity in disease burden, health systems and socio-economic development of China. The parameters were reliable and stable, which were estimated based on the pooled Chinese databases from multi-centre studies in rural and urban areas of 9 provinces across China . Moreover, we used the most recently updated data from National Bureau of Statistics , China Cancer Registry  and Statistics of National Health and Family Planning Commission .
Limitations also exist in the methods. Firstly, the model did not capture the indirect protection resulting from the herd immunity caused by the reduction of circulation of the infective agent . As a result, the benefits of the vaccination could be underestimated. Secondly, the vaccine efficacy in our model was assumed to be life-long, however,but the vaccine efficacy clinical trials have only lasted less than 10 years, so the duration of vaccine efficacy is unknown. Thirdly, the end study analysis of clinical registration trials of HPV vaccines in China are ongoing [9, 10] and no final data for the vaccine efficacy against CIN2/3+ irrespective of HPV types are available, so we adopted 93 % vaccine efficacy from PATRICIA trial . The assumption of lifelong duration of vaccination and the high efficacy could overestimate the benefits of vaccination and result in more favourable ICERs. Fourthly, one of the uncertainties we have is whether HPV type replacement take place once vaccination against HPV-16/18 is widespread. The prevalence of HPV-16/18 falls to very low levels with vaccination. Other oncogenic HPV subtypes currently responsible for relatively few CC cases, might fill the niche left by HPV-16/18. To date this question could not be answered but available evidence suggests that niche competition is unlikely to happen . Lastly, the present model only included cervical cancer and pre-cancer, irrespective of the vulvar cancer, vaginal cancer, anal and some proportion of oropharyngeal cancer cancers that the HPV vaccine may have efficacy in preventing [78, 79, 80]. If these diseases were included in the evaluation, the protection offered by HPV vaccination would be wider, and would lead to a lower ICER than the present analyses. These results are thus likely to provide a conservative estimate.
In both rural and urban areas, the vaccination cost and discounting are important factors determining the cost-effectiveness of HPV vaccination; policy makers in China should take these into account when making a decision on the introduction of HPV vaccine. In areas with a high burden of cervical cancer and limited screening activities, HPV vaccination should be prioritized. However, the vaccine cost needs to be reduced in order to make it very cost-effective and affordable as well, in particular in poverty areas with high disease burden.
The authors would like to acknowledge Dr Filip Meheus, Dr R. Sankaranarayanan from International Agency for Research on Cancer and Dr Youlin Qiao from CICAMS for their very valuable advice on the manuscript; XF Pan from Western China Medical College for his assistance in early preparation of the study. GlaxoSmithKline Health Economic Team for providing research funding and the vaccine related data.
This study received funding from GlaxoSmithKline Biologicals SA; National Natural Science Foundation of China (81322040) and NIH Fogarty International Center Grant (#5R25TW009340).
Availability of data and materials
The main data analyzed during this study are included in this published article and its supplementary information files. The datasets during the current study are available from the corresponding author on reasonable request.
FH Zhao and SY Hu conceived and designed the study; Q Zhang and SY Hu collected the data; YJ Liu and Q Zhang run the model and analyzed data; Q Zhang and YJ Liu drafted the manuscript; all authors reviewed, commented on drafts, and approved the final manuscript.
The institution of Q Zhang, SY Hu and FH Zhao received the research funding from GlaxoSmithKline Biologicals SA, however, the study design, data analyses and data interpretation were conducted by all authors independently.
Consent for publication
Ethics approval and consent to participate
This study was approved by the Human Subjects Review Boards (Approval No. 13-066/742) of the CICAMS. The study population was a hypothetical cohort of 12-55 year old girls. The parameters in this modelling study were collected by expert review panel, literature review and data extraction from previous studies conducted by CICAMS with the permission to use the summary forms of these data, so no individual patient information were involved, and informed consent was exempted by CICAMS’ IRB.
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