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“Social Inequities in Cancer” is a compendium of articles that identify barriers and metrics on the topic of modifiable and unnecessary cancer inequalities. Social inequities have long been recognised as a strong contributing factor in health and cancer inequalities for the past several decades. Despite progress in cancer treatment, cancer incidence, mortality and survival vary markedly between and within countries. Globalisation, greater life expectancy, emerging analytical technologies, and the scalability of big data have revolutionized the vantage point from which social inequities can be studied. The focus of these articles is inequalities as they relate to cancer, with the inequalities ranging from the community to the global scale. Disclaimer: Where authors are identified as personnel of the International Agency for Research on Cancer / World Health Organization, the authors alone are responsible for the views expressed in this article and they do not necessarily represent the decisions, policy or views of the International Agency for Research on Cancer / World Health Organization.
Population-based cancer registries are an essential information source for quantifying the impact of cancer in a population and its evolution, planning and evaluation of cancer control policies and healthcare systems. In the last decades, the information provided by cancer registries has improved dramatically in quality and quantity. Technological advances and record linkage have contributed to data improvement. Therefore, clinical data collected by cancer registries such as stage, treatment, co-morbidity, etc. contribute to treatment effectiveness assessment and identification of inequality in health care access at the population level. The reliability and utility of the information provided by cancer registries depend on the quality of the data collected. On the other hand, cancer registries' data harmonisation is crucial for data use and comparability.
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