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      Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population Women

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          Updating cost-effectiveness--the curious resilience of the $50,000-per-QALY threshold.

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            Global cancer transitions according to the Human Development Index (2008-2030): a population-based study.

            Cancer is set to become a major cause of morbidity and mortality in the coming decades in every region of the world. We aimed to assess the changing patterns of cancer according to varying levels of human development. We used four levels (low, medium, high, and very high) of the Human Development Index (HDI), a composite indicator of life expectancy, education, and gross domestic product per head, to highlight cancer-specific patterns in 2008 (on the basis of GLOBOCAN estimates) and trends 1988-2002 (on the basis of the series in Cancer Incidence in Five Continents), and to produce future burden scenario for 2030 according to projected demographic changes alone and trends-based changes for selected cancer sites. In the highest HDI regions in 2008, cancers of the female breast, lung, colorectum, and prostate accounted for half the overall cancer burden, whereas in medium HDI regions, cancers of the oesophagus, stomach, and liver were also common, and together these seven cancers comprised 62% of the total cancer burden in medium to very high HDI areas. In low HDI regions, cervical cancer was more common than both breast cancer and liver cancer. Nine different cancers were the most commonly diagnosed in men across 184 countries, with cancers of the prostate, lung, and liver being the most common. Breast and cervical cancers were the most common in women. In medium HDI and high HDI settings, decreases in cervical and stomach cancer incidence seem to be offset by increases in the incidence of cancers of the female breast, prostate, and colorectum. If the cancer-specific and sex-specific trends estimated in this study continue, we predict an increase in the incidence of all-cancer cases from 12·7 million new cases in 2008 to 22·2 million by 2030. Our findings suggest that rapid societal and economic transition in many countries means that any reductions in infection-related cancers are offset by an increasing number of new cases that are more associated with reproductive, dietary, and hormonal factors. Targeted interventions can lead to a decrease in the projected increases in cancer burden through effective primary prevention strategies, alongside the implementation of vaccination, early detection, and effective treatment programmes. None. Copyright © 2012 Elsevier Ltd. All rights reserved.
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              Next-generation DNA sequencing.

              DNA sequence represents a single format onto which a broad range of biological phenomena can be projected for high-throughput data collection. Over the past three years, massively parallel DNA sequencing platforms have become widely available, reducing the cost of DNA sequencing by over two orders of magnitude, and democratizing the field by putting the sequencing capacity of a major genome center in the hands of individual investigators. These new technologies are rapidly evolving, and near-term challenges include the development of robust protocols for generating sequencing libraries, building effective new approaches to data-analysis, and often a rethinking of experimental design. Next-generation DNA sequencing has the potential to dramatically accelerate biological and biomedical research, by enabling the comprehensive analysis of genomes, transcriptomes and interactomes to become inexpensive, routine and widespread, rather than requiring significant production-scale efforts.
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                Author and article information

                Journal
                JNCI: Journal of the National Cancer Institute
                Oxford University Press (OUP)
                0027-8874
                1460-2105
                July 2018
                July 01 2018
                January 18 2018
                July 2018
                July 01 2018
                January 18 2018
                : 110
                : 7
                : 714-725
                Affiliations
                [1 ]Centre for Experimental Cancer Medicine, Queen Mary University of London, London, UK
                [2 ]Department of Gynaecological Oncology, Barts Health NHS Trust, Royal London Hospital, London, UK
                [3 ]Gynaecological Cancer Research Centre, Department of Women’s Cancer, Institute for Women’s Health, University College London, London, UK
                [4 ]Department of Health Services Research and Policy, London School of Hygiene and Tropical Medicine, London, UK
                [5 ]Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, UK
                [6 ]Centre for Cancer Genetic Epidemiology, University of Cambridge, Strangeways Research Laboratory, Worts Causeway, Cambridge, UK
                [7 ]Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Victoria, Australia
                [8 ]Barts Cancer Institute, Queen Mary University of London, London, UK
                [9 ]Faculty of Medicine, School of Women’s and Children’s Health, University of New South Wales, Sydney, Australia
                [10 ]The Kinghorn Cancer Centre, Garvan Institute of Medical Research, Australia
                [11 ]Cedars Sinai Medical Centre, Los Angeles, CA
                [12 ]University of New South Wales, Sydney, NSW, Australia
                Article
                10.1093/jnci/djx265
                29361001
                1e901864-6d25-4966-a66e-7087a280e426
                © 2018

                http://academic.oup.com/journals/pages/about_us/legal/notices

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