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Cancer incidence estimation from mortality data: a validation study within a population-based cancer registry

dc.contributor.authorRedondo-Sánchez, Daniel
dc.contributor.authorRodríguez-Barranco, Miguel
dc.contributor.authorAmeijide, Alberto
dc.contributor.authorAlonso, Francisco Javier
dc.contributor.authorFernandez-Navarro, Pablo L
dc.contributor.authorJimenez-Moleon, Jose J.
dc.contributor.authorSánchez, María-José
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERESP (Epidemiología y Salud Pública)
dc.contributor.funderRegional Government of Andalusia (España)
dc.date.accessioned2022-03-30T09:35:08Z
dc.date.available2022-03-30T09:35:08Z
dc.date.issued2021
dc.description.abstractBackground: Population-based cancer registries are required to calculate cancer incidence in a geographical area, and several methods have been developed to obtain estimations of cancer incidence in areas not covered by a cancer registry. However, an extended analysis of those methods in order to confirm their validity is still needed. Methods: We assessed the validity of one of the most frequently used methods to estimate cancer incidence, on the basis of cancer mortality data and the incidence-to-mortality ratio (IMR), the IMR method. Using the previous 15-year cancer mortality time series, we derived the expected yearly number of cancer cases in the period 2004-2013 for six cancer sites for each sex. Generalized linear mixed models, including a polynomial function for the year of death and smoothing splines for age, were adjusted. Models were fitted under a Bayesian framework based on Markov chain Monte Carlo methods. The IMR method was applied to five scenarios reflecting different assumptions regarding the behavior of the IMR. We compared incident cases estimated with the IMR method to observed cases diagnosed in 2004-2013 in Granada. A goodness-of-fit (GOF) indicator was formulated to determine the best estimation scenario. Results: A total of 39,848 cancer incidence cases and 43,884 deaths due to cancer were included. The relative differences between the observed and predicted numbers of cancer cases were less than 10% for most cancer sites. The constant assumption for the IMR trend provided the best GOF for colon, rectal, lung, bladder, and stomach cancers in men and colon, rectum, breast, and corpus uteri in women. The linear assumption was better for lung and ovarian cancers in women and prostate cancer in men. In the best scenario, the mean absolute percentage error was 6% in men and 4% in women for overall cancer. Female breast cancer and prostate cancer obtained the worst GOF results in all scenarios. Conclusion: A comparison with a historical time series of real data in a population-based cancer registry indicated that the IMR method is a valid tool for the estimation of cancer incidence. The goodness-of-fit indicator proposed can help select the best assumption for the IMR based on a statistical argument.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis research was supported with the subprogram “Cancer surveillance” of the CIBER of Epidemiology and Public Health (CIBERESP). This work has been also partially supported by grant PGC2018-098860-B-I00 (MINECO/FEDER). M. J. Sánchez is supported by the Andalusian Department of Health Research, Development and Innovation, project grant PI-0152/2017.es_ES
dc.format.number1es_ES
dc.format.page18es_ES
dc.format.volume19es_ES
dc.identifier.citationPopul Health Metr. 2021;19(1):18.es_ES
dc.identifier.doi10.1186/s12963-021-00248-1es_ES
dc.identifier.e-issn1478-7954es_ES
dc.identifier.journalPopulation Health Metricses_ES
dc.identifier.pubmedID33757540es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/13906
dc.language.isoenges_ES
dc.publisherBioMed Central (BMC)
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PGC2018-098860-B-I00es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/PI-0152/2017es_ES
dc.relation.publisherversionhttps://doi.org/10.1186/s12963-021-00248-1es_ES
dc.repisalud.centroISCIII::Centro Nacional de Epidemiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCancer incidencees_ES
dc.subjectEstimationes_ES
dc.subjectGoodness-of-fites_ES
dc.subjectMortality-to-incidence ratioes_ES
dc.subjectValidationes_ES
dc.titleCancer incidence estimation from mortality data: a validation study within a population-based cancer registryes_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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Table S1. Observed cases and expected cases under each scenario, and goodness of fit measures. Men.
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Table S2. Observed cases and expected cases under each scenario, and goodness of fit measures. Women
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Fig. S1. Design of the data used in the iterative procedure to derived the incidence time series
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Fig. S2. Number of observed and expected (with 95% CI) cases under the best scenario for each site. Men