Estimating incidence for rare cancers (RC) is challenging for exceptionally rare entities and in small populations. In a previous study, the RARECAREnet project provided Bayesian estimates of the expected number… Click to show full abstract
Estimating incidence for rare cancers (RC) is challenging for exceptionally rare entities and in small populations. In a previous study, the RARECAREnet project provided Bayesian estimates of the expected number of RCs and their 95% credible intervals for 27 European countries using data collected by population-based cancer registries. In that study, slightly different results were found by implementing a Poisson model in INLA/WinBUGS platforms. This paper has assessed the performance of a Poisson modelling approach for estimating RC incidence rates, oscillating around an overall European average and using small counts data in different scenarios/computational platforms. First, we compared the performance of Frequentist, Empirical Bayes and Bayesian approaches for providing 95% confidence/credible intervals for the expected rates in each country. Second, we carried out an empirical study using 190 RCs for assessing different lower/upper bounds of a uniform prior distribution for the standard deviation of the random effects. To obtain a reliable measure of variability for country-specific incidence rates, our results suggest the suitability of using 1 as lower bound for that prior distribution and selecting the random effects model through an averaged indicator derived from two Bayesian model selection criterions, the Deviance and Watanabe-Akaike Information Criterions (DIC and WAIC, respectively).
               
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