Abstract
Population-based data are increasingly used to elucidate the burden of cancer worldwide. Incidence and mortality data from regional and national cancer registries should allow researchers to monitor trends and disparities in cancer occurrence, survival, and mortality in populations and subgroups of the population and to evaluate the effectiveness of screening for cancers amenable to early detection and treatment. Given that the primary purpose of screening is to reduce the number of deaths attributable to cancer, cancer mortality is assumed to be the most important indicator of the effectiveness of screening and the most basic measure of progress against cancer (Hakama et al. 2008; Jatoi and Miller 2003). In setting screening policy, the deaths saved by screening, however, must be weighed against any adverse effects of screening resulting from over identifying or over treating cases, as well as monetary costs.
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This work was supported by grant T32AG0037 from the National Institute on Aging to the University of Southern California.
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Garcia, K., Crimmins, E.M. (2013). Cancer Screening in the U.S. and Europe: Policies, Practices, and Trends in Cancer Incidence and Mortality. In: Hoque, N., McGehee, M., Bradshaw, B. (eds) Applied Demography and Public Health. Applied Demography Series, vol 3. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-6140-7_9
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