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      Oral primary care: an analysis of its impact on the incidence and mortality rates of oral cancer

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          Abstract

          Background

          Oral cancer is a potentially fatal disease, especially when diagnosed in advanced stages. In Brazil, the primary health care (PHC) system is responsible for promoting oral health in order to prevent oral diseases. However, there is insufficient evidence to assess whether actions of the PHC system have some effect on the morbidity and mortality from oral cancer. The purpose of this study was to analyze the effect of PHC structure and work processes on the incidence and mortality rates of oral cancer after adjusting for contextual variables.

          Methods

          An ecological, longitudinal and analytical study was carried out. Data were obtained from different secondary data sources, including three surveys that were nationally representative of Brazilian PHC and carried out over the course of 10 years (2002–2012). Data were aggregated at the state level at different times. Oral cancer incidence and mortality rates, standardized by age and gender, served as the dependent variables. Covariables (sociodemographic, structure of basic health units, and work process in oral health) were entered in the regression models using a hierarchical approach based on a theoretical model. Analysis of mixed effects with random intercept model was also conducted (alpha = 5%).

          Results

          The oral cancer incidence rate was positively association with the proportion of of adults over 60 years (β = 0.59; p = 0.010) and adult smokers (β = 0.29; p = 0.010). The oral cancer related mortality rate was positively associated with the proportion of of adults over 60 years (β = 0.24; p < 0.001) and the performance of preventative and diagnostic actions for oral cancer (β = 0.02; p = 0.002). Mortality was inversely associated with the coverage of primary care teams (β = −0.01; p < 0.006) and PHC financing (β = −0.52 −9; p = 0.014).

          Conclusions

          In Brazil, the PHC structure and work processes have been shown to help reduce the mortality rate of oral cancer, but not the incidence rate of the disease. We recommend expanding investments in PHC in order to prevent oral cancer related deaths.

          Electronic supplementary material

          The online version of this article (10.1186/s12885-017-3700-z) contains supplementary material, which is available to authorized users.

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          Most cited references58

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          Aging, Cellular Senescence, and Cancer

          For most species, aging promotes a host of degenerative pathologies that are characterized by debilitating losses of tissue or cellular function. However, especially among vertebrates, aging also promotes hyperplastic pathologies, the most deadly of which is cancer. In contrast to the loss of function that characterizes degenerating cells and tissues, malignant (cancerous) cells must acquire new (albeit aberrant) functions that allow them to develop into a lethal tumor. This review discusses the idea that, despite seemingly opposite characteristics, the degenerative and hyperplastic pathologies of aging are at least partly linked by a common biological phenomenon: a cellular stress response known as cellular senescence. The senescence response is widely recognized as a potent tumor suppressive mechanism. However, recent evidence strengthens the idea that it also drives both degenerative and hyperplastic pathologies, most likely by promoting chronic inflammation. Thus, the senescence response may be the result of antagonistically pleiotropic gene action.
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            Senescence-associated inflammatory responses: aging and cancer perspectives.

            Senescent cells, albeit not proliferating, are metabolically and transcriptionally active, thereby capable of affecting their microenvironment, notably via the production of inflammatory mediators. These mediators maintain and propagate the senescence process to neighboring cells, and then recruit immune cells for clearing senescent cells. Among the inflammatory cues are molecules with pronounced tumor-controlling properties, both growth and invasion factors and inhibitory factors, working directly or via recruited immune cells. These senescence-inflammatory effects also prevail within tumors, mediated by the senescent tumor cells and the senescent tumor stroma. Here, we review the course and impact of senescence-associated inflammatory responses in aging and cancer. We propose that controlling senescence-associated inflammation by targeting specific inflammatory mediators may have a beneficial therapeutic effect in treatment of cancer and aging-related diseases.
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              The role of outcomes in quality assessment and assurance.

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                Author and article information

                Contributors
                rochahernandes3@gmail.com
                ebthomaz@globo.com
                nubiacristina@gmail.com
                queiroz.rejane@gmail.com
                martary@gmail.com
                allan@ufmg.br
                elainethume@gmail.com
                joao096victor@gmail.com
                viviane_alvares@yahoo.com.br
                dante@medomai.com.br
                jnv4@duke.edu
                catherine.staton@duke.edu
                luizfacchini@gmail.com
                Journal
                BMC Cancer
                BMC Cancer
                BMC Cancer
                BioMed Central (London )
                1471-2407
                30 October 2017
                30 October 2017
                2017
                : 17
                : 706
                Affiliations
                [1 ]ISNI 0000 0001 2181 4888, GRID grid.8430.f, Federal University of Minas Gerais, School of Economics, Center of post-graduate and Research in Administration, ; Belo Horizonte, Minas Gerais Brazil
                [2 ]ISNI 0000 0001 2165 7632, GRID grid.411204.2, Department of Public Health, , Federal University of Maranhão, ; São Luís, Maranhão Brazil
                [3 ]ISNI 0000000121511713, GRID grid.10772.33, National School of Public Health, , Nova University of Lisbon, ; Lisboa, Portugal
                [4 ]ISNI 0000 0001 2192 5801, GRID grid.411195.9, Department of Public Health, , Federal University of Goiás, ; Goiânia, Goiás, Brazil
                [5 ]ISNI 0000 0001 2181 4888, GRID grid.8430.f, Faculty of Economics, Department of Administrative Sciences, , Federal University of Minas Gerais, ; Belo Horizonte, Minas Gerais Brazil
                [6 ]ISNI 0000 0001 2134 6519, GRID grid.411221.5, Faculty of Nursing, Department of Collective Health, , Federal University of Pelotas, ; Pelotas, Rio Grande do Sul Brazil
                [7 ]Medomai Information Technology Systems, Belo Horizonte, Minas Gerais Brazil
                [8 ]ISNI 0000 0004 1936 7961, GRID grid.26009.3d, Duke Division of Emergency Medicine, Duke University Health System, Duke Global Health Institute, , Duke University, ; Durham, USA
                [9 ]ISNI 0000 0004 1936 7961, GRID grid.26009.3d, Duke Division of Emergency Medicine, Duke University Health System, Duke Global Health Institute, , Duke University, ; Durham, USA
                [10 ]ISNI 0000 0001 2134 6519, GRID grid.411221.5, Faculty of Medicine, Department of Social Medicine, , Federal University of Pelotas, ; Pelotas, Rio Grande do Sul Brazil
                [11 ]ISNI 0000 0001 2181 4888, GRID grid.8430.f, Business Administration Department – Observatory of human resources for health, , Universidade Federal de Minas Gerais, ; Antonio Carlos, avenue, 6627, Belo Horizonte, Minas Gerais Brazil
                Article
                3700
                10.1186/s12885-017-3700-z
                5661925
                29084516
                50e4acec-95d5-45d5-a3b2-1d760995a5fc
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 26 July 2016
                : 22 October 2017
                Funding
                Funded by: Brazilian Ministry of Health
                Funded by: FundRef http://dx.doi.org/10.13039/100000061, Fogarty International Center;
                Award ID: K01 TW010000-01A1
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2017

                Oncology & Radiotherapy
                health systems,health inequalities,mortality,mouth neoplasms,ecological studies,primary health care,program evaluation

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