Literature DB >> 22409292

Selecting a mix of prevention strategies against cervical cancer for maximum efficiency with an optimization program.

Nadia Demarteau1, Thomas Breuer, Baudouin Standaert.   

Abstract

BACKGROUND: Screening and vaccination against human papillomavirus (HPV) can protect against cervical cancer. Neither alone can provide 100% protection. Consequently it raises the important question about the most efficient combination of screening at specified time intervals and vaccination to prevent cervical cancer.
OBJECTIVE: Our objective was to identify the mix of cervical cancer prevention strategies (screening and/or vaccination against HPV) that achieves maximum reduction in cancer cases within a fixed budget.
METHODS: We assessed the optimal mix of strategies for the prevention of cervical cancer using an optimization program. The evaluation used two models. One was a Markov cohort model used as the evaluation model to estimate the costs and outcomes of 52 different prevention strategies. The other was an optimization model in which the results of each prevention strategy of the previous model were entered as input data. The latter model determined the combination of the different prevention options to minimize cervical cancer under budget, screening coverage and vaccination coverage constraints. We applied the model in two countries with different healthcare organizations, epidemiology, screening practices, resource settings and treatment costs: the UK and Brazil. 100,000 women aged 12 years and above across the whole population over a 1-year period at steady state were included. The intervention was papanicolaou (Pap) smear screening programmes and/or vaccination against HPV with the bivalent HPV 16/18 vaccine (Cervarix® [Cervarix is a registered trademark of the GlaxoSmithKline group of companies]). The main outcome measures were optimal distribution of the population between different interventions (screening, vaccination, screening plus vaccination and no screening or vaccination) with the resulting number of cervical cancer and associated costs.
RESULTS: In the base-case analysis (= same budget as today), the optimal prevention strategy would be, after introducing vaccination with a coverage rate of 80% in girls aged 12 years and retaining screening coverage at pre-vaccination levels (65% in the UK, 50% in Brazil), to increase the screening interval to 6 years (from 3) in the UK and to 5 years (from 3) in Brazil. This would result in a reduction of cervical cancer by 41% in the UK and by 54% in Brazil from pre-vaccination levels with no budget increase. Sensitivity analysis shows that vaccination alone at 80% coverage with no screening would achieve a cervical cancer reduction rate of 20% in the UK and 43% in Brazil compared with the pre-vaccination situation with a budget reduction of 30% and 14%, respectively. In both countries, the sharp reduction in cervical cancer is seen when the vaccine coverage rate exceeds the maximum screening coverage rate, or when screening coverage rate exceeds the maximum vaccine coverage rate, while maintaining the budget. As with any model, there are limitations to the value of predictions depending upon the assumptions made in each model.
CONCLUSIONS: Spending the same budget that was used for screening and treatment of cervical cancer in the pre-vaccination era, results of the optimization program show that it would be possible to substantially reduce the number of cases by implementing an optimal combination of HPV vaccination (80% coverage) and screening at pre-vaccination coverage (65% UK, 50% Brazil) while extending the screening interval to every 6 years in the UK and 5 years in Brazil.

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Year:  2012        PMID: 22409292     DOI: 10.2165/11591560-000000000-00000

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  37 in total

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Review 2.  Chapter 8: Screening for cervical cancer in developing countries.

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3.  Impact of human papillomavirus (HPV)-6/11/16/18 vaccine on all HPV-associated genital diseases in young women.

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Review 4.  HPV vaccine: Cervarix.

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5.  Quadrivalent vaccine against human papillomavirus to prevent anogenital diseases.

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Review 7.  Economic evaluation of human papillomavirus vaccination in developed countries.

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Review 8.  Cervical cancer screening following prophylactic human papillomavirus vaccination.

Authors:  Eduardo L Franco; Jack Cuzick
Journal:  Vaccine       Date:  2008-03-14       Impact factor: 3.641

9.  Intracellular surveillance of persisting viral infections. Human genital cancer results from deficient cellular control of papillomavirus gene expression.

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10.  High sustained efficacy of a prophylactic quadrivalent human papillomavirus types 6/11/16/18 L1 virus-like particle vaccine through 5 years of follow-up.

Authors:  L L Villa; R L R Costa; C A Petta; R P Andrade; J Paavonen; O-E Iversen; S-E Olsson; J Høye; M Steinwall; G Riis-Johannessen; A Andersson-Ellstrom; K Elfgren; G von Krogh; M Lehtinen; C Malm; G M Tamms; K Giacoletti; L Lupinacci; R Railkar; F J Taddeo; J Bryan; M T Esser; H L Sings; A J Saah; E Barr
Journal:  Br J Cancer       Date:  2006-11-21       Impact factor: 7.640

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  20 in total

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Review 2.  Implementation science and its application to population health.

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Review 4.  Adolescent human papillomavirus vaccination in the United States: Opportunities for integrating pharmacies into the immunization neighborhood.

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5.  Budget constraint and vaccine dosing: a mathematical modelling exercise.

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6.  Health economic analysis of human papillomavirus vaccines in women of Chile: perspective of the health care payer using a Markov model.

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7.  Ethical considerations of universal vaccination against human papilloma virus.

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Journal:  BMC Med Ethics       Date:  2014-04-07       Impact factor: 2.652

8.  Modeling optimal cervical cancer prevention strategies in Nigeria.

Authors:  Nadia Demarteau; Imran O Morhason-Bello; Babatunde Akinwunmi; Isaac F Adewole
Journal:  BMC Cancer       Date:  2014-05-24       Impact factor: 4.430

9.  Urban and rural safety net health care system clinics: no disparity in HPV4 vaccine completion rates.

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Journal:  PLoS One       Date:  2014-05-09       Impact factor: 3.240

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