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Cancer registration

Its uses in research, and confidentiality in the EC

Bibliographic Data

ID11171206
AuthorsC A Stiller, Charles Stiller (0000-0002-3006-7869, University of Oxford, corresponding author)
Year1993
Volume47
Issue5
Pages342-344
Publication date1993-10-01
Open AccessNo
TypeARTICLE
VenueJournal of Epidemiology and Community Health (JOURNAL)
Journal identifiersISSN: 0143-005X • E-ISSN: 1470-2738
PublisherBMJ (PUBLISHER • GB)
DOI10.1136/jech.47.5.342
PMID8289030
OpenAlexW2034378285
LanguageEN
Citations received1
References cited3

Cancer registration in England and Wales was begun in 1929 by the Radium Commission. The work was transferred to the General Register Office in 1947 and thence to its successor, the Office of Population Censuses and Surveys (OPCS). National coverage, though not 100% registration, was achieved in 1962. Meanwhile a parallel system was established in Scotland, cover- ing the whole country by 1959. The National Cancer Registry in England and Wales is the largest population-based registry in the world, containing over five million case records; though it is inevitable that some cancers will escape registration, studies of selected groups indicate a high degree of completeness of ascertainment.' 2

Cancer registry · Commission · Confidentiality · Environmental health · Family medicine · Political science · Population · Economic and Financial Impacts of Cancer · Global Cancer Incidence and Screening · Law · Medicine

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Citations per year0.25
Citation span2022 - 2022 (1)
Highly citedNo

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