Elsevier

Vaccine

Volume 24, Supplement 3, 21 August 2006, Pages S155-S163
Vaccine

Chapter 18: Public health policy for cervical cancer prevention: The role of decision science, economic evaluation, and mathematical modeling

https://doi.org/10.1016/j.vaccine.2006.05.112Get rights and content

Abstract

Several factors are changing the landscape of cervical cancer control, including a better understanding of the natural history of human papillomavirus (HPV), reliable assays for detecting high-risk HPV infections, and a soon to be available HPV-16/18 vaccine. There are important differences in the relevant policy questions for different settings. By synthesizing and integrating the best available data, the use of modeling in a decision analytic framework can identify those factors most likely to influence outcomes, can guide the design of future clinical studies and operational research, can provide insight into the cost-effectiveness of different strategies, and can assist in early decision-making when considered with criteria such as equity, public preferences, and political and cultural constraints.

Introduction

When making decisions we can either base choices on evidence and the explicit comparison of alternative strategies or we can use the intuitive opinions of experts. Decision science provides a quantitative framework for evaluating available evidence and uses explicit models to synthesize data, acknowledge uncertainty, and extrapolate from specific studies [1].

Several innovations are changing the landscape for cervical cancer prevention and control, with important differences in the most relevant policy questions for different settings. In countries with existing screening programs, pressing questions center around the optimal use of HPV-DNA testing, reducing disparities, and defining synergies between screening and vaccination. Important questions in low-resource settings include how to implement and sustain screening strategies with fewer technical and infrastructure requirements than required by conventional cytology-based programs, how to target the appropriate age groups for screening, and how to overcome the logistical barriers associated with delivering a three-dose vaccine during early adolescence. Key questions include: what is the coverage that could realistically be achieved with screening between ages 35 and 40 versus vaccination at ages 10–12? Will both boys and girls need to be vaccinated? Is there a combined screening/vaccination strategy that could be cost-effective or will decision makers need to choose between the two?

No single empirical study can evaluate all possible strategies to inform these complex policy questions. By integrating the best biologic, epidemiologic, economic, and behavioral data, the use of modeling in a decision analytic framework can assist in early decision-making, can highlight where better data are needed and identify those factors most likely to influence outcomes, can inform clinical study design and guide the conduct of operational research, and can provide insight into the potential cost-effectiveness of different strategies. Here we review the elements of cost-effectiveness analysis and identify the methodological issues most relevant to upcoming policy questions in the cervical cancer field.

Section snippets

Decision analysis and cost-effectiveness analysis

Decision science offers an explicit, quantitative, and systematic approach to decision-making under uncertainty [1]. A collection of quantitative methods is used to guide the management of complex problems that involve competing choices, different perspectives, and trade-offs. The premise of a decision analytic approach is that all consequences of decisions should be identified, measured, and valued while also considering the uncertainty that exists about the outcomes at the time decisions are

Reporting the results of a cost-effectiveness analysis

Cost-effectiveness results are often displayed in the format of an efficiency curve, as shown in Fig. 3, where the lifetime costs and clinical benefits (discounted life expectancy on the left vertical axis, reduction in lifetime risk of cancer on the right vertical axis) of different screening strategies performed at different screening intervals are shown. Strategies lying on the efficiency curve dominate those lying to the right of the curve because they are more effective, and either cost

Interpreting the results of a cost-effectiveness analysis

While interventions that improve health at a cost should ideally be compared with other interventions that compete for the same resources, there is no universal criterion that defines a threshold cost-effectiveness ratio, below which an intervention would be considered cost-effective. A commonly-cited rule of thumb is based on a report by the Commission on Macroeconomics and Health (CMH), and subsequent recommendations that interventions are “very cost-effective” and “cost-effective” if they

Use of models

Models can be classified along several dimensions: according to the structure used for events that occur over time (e.g., decision trees, state transition models); whether they are open or closed and according to the nature of the target population (e.g., a longitudinal cohort model, cross-sectional population model); by the method of calculation (e.g., deterministic, stochastic); and whether they reflect the transmission dynamics of infection [3], [16], [17]. Models utilize a wide range of

Conclusion

Evaluating the effectiveness of a public health prevention program is complex, particularly when the course from infection to disease spans multiple decades, when new activities are building upon existing interventions, and when resource constraints limit the range of reasonable choices. Decision science and cost-effectiveness analyses offer important tools that can help to address key cervical cancer policy questions relating to screening and vaccination.

Disclosed potential conflicts of interest

GPG: Consultant (GlaxoSmithKline, Merck and Co., Inc., Sanofi-Pasteur MSD, Sanofi-Pasteur); Research Grants (GlaxoSmithKline)

Acknowledgments

Dr. Goldie is supported in part by the US National Cancer Insitute (grant #R01 CA093435) and The Bill and Melinda Gates Foundation (grant #30505). Mr. Goldhaber-Fiebert is supported in part by a National Science Foundation Graduate Research Fellowship. We gratefully acknowledge the valuable contributions of Steven Sweet and Meredith Holtan of the Harvard School of Public Health, Boston, MA, for their outstanding technical assistance.

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