
Contents
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7.1 Background 7.1 Background
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7.2 Monitoring incidence, survival and mortality 7.2 Monitoring incidence, survival and mortality
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7.3 UKCCSG and Childhood Leukaemia Working Party Collaboration 7.3 UKCCSG and Childhood Leukaemia Working Party Collaboration
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7.4 Geographical epidemiology 7.4 Geographical epidemiology
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7.5 The NRCT as a source of case (and control) data 7.5 The NRCT as a source of case (and control) data
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7.6 Individual record linkage studies 7.6 Individual record linkage studies
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7.7 Other functions of the registry 7.7 Other functions of the registry
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7.8 The future 7.8 The future
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Cite
Abstract
In addition to the detailed descriptive analyses of childhood cancer incidence, survival and mortality that are presented in this book, the registry data have contributed to international studies of incidence and survival. Detailed geographical information on the cases in the registry has been used to study variations in incidence in relation to environmental factors that also vary geographically, and to ecological features of small areas such as socioeconomic status, urban/rural status and population density. Some aetiological studies make use of birth registration details which are held for most children in the registry and for matched control children. Aetiology has also been investigated through record linkage studies. The relation between patterns of care and survival from childhood cancer has been investigated in a series of studies. The registry is a resource for a wide range of information and statistics on childhood cancer in the UK.
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