NORDCAN – a Nordic tool for cancer information, planning, quality control and research

Authors

  • Gerda Engholm NORDCAN secretariat, Danish Cancer Society, Copenhagen, Denmark; Department of Cancer Prevention & Documentation, Danish Cancer Society, Copenhagen, Denmark
  • Jacques Ferlay Data Analysis and Interpretation Group, Cancer Information Section, International Agency for Research on Cancer, Lyon, France
  • Niels Christensen NORDCAN secretariat, Danish Cancer Society, Copenhagen, Denmark; Department of Cancer Prevention & Documentation, Danish Cancer Society, Copenhagen, Denmark
  • Freddie Bray Department of Clinical- and Registry-based Research, Cancer Registry of Norway, Oslo, Norway; Department of Biostatistics, Institute of Basic Medical Sciences, University of Oslo, Norway
  • Marianne L. Gjerstorff Danish Cancer Registry, National Board of Health, Copenhagen, Denmark
  • Åsa Klint Swedish Cancer Registry, National Board of Health and Welfare, Stockholm, Sweden
  • Jóanis E. Køtlum Faroe Islands Cancer Registry, Tórshavn, Faroe Islands
  • Elínborg Ólafsdóttir Icelandic Cancer Registry, Reykjavik, Iceland
  • Eero Pukkala Institute for Statistical and Epidemiologic Cancer Research, Finnish Cancer Registry, Helsinki, Finland
  • Hans H. Storm NORDCAN secretariat, Danish Cancer Society, Copenhagen, Denmark; Department of Cancer Prevention & Documentation, Danish Cancer Society, Copenhagen, Denmark

DOI:

https://doi.org/10.3109/02841861003782017

Abstract

The NORDCAN database and program (www.ancr.nu) include detailed information and results on cancer incidence, mortality and prevalence in each of the Nordic countries over five decades and has lately been supplemented with predictions of cancer incidence and mortality; future extensions include the incorporation of cancer survival estimates. Material and methods. The data originates from the national cancer registries and causes of death registries in Denmark, Finland, Iceland, Norway, Sweden, and Faroe Islands and is regularly updated. Presently 41 cancer entities are included in the common dataset, and conversions of the original national data according to international rules ensure comparability. Results. With 25 million inhabitants in the Nordic countries, 130 000 incident cancers are reported yearly, alongside nearly 60 000 cancer deaths, with almost a million persons living with a cancer diagnosis. This web-based application is available in English and in each of the five Nordic national languages. It includes comprehensive and easy-to-use descriptive epidemiology tools that provide tabulations and graphs, with further user-specified options available. Discussion. The NORDCAN database aims to provide comparable and timely data to serve the varying needs of policy makers, cancer societies, the public, and journalists, as well as the clinical and research community.

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Published

2010-01-01

How to Cite

Engholm, G., Ferlay, J., Christensen, N., Bray, F., Gjerstorff, M. L., Klint, Åsa, … Storm, H. H. (2010). NORDCAN – a Nordic tool for cancer information, planning, quality control and research. Acta Oncologica, 49(5), 725–736. https://doi.org/10.3109/02841861003782017