Department of Health

Website of the Department of Health

Please note that this website has a UK government access keys system.

You are here:

Cancer registries

6.24 Cancer registries collect population based data on the incidence, survival and mortality from cancer.

These data can help to identify the causes of cancer leading to strategies for prevention. Cancer registry information is also vital for assessing the effectiveness of screening programmes and cancer treatment services in improving survival rates and reducing mortality.

6.25 These public health benefits depend on the completeness of cancer registration in the population. The government is determined to secure the future of cancer registration and will take the necessary action to ensure this.

6.26 Earlier this year, Professor Charles Gillis, Director of the West of Scotland Cancer Surveillance Unit completed a major review of cancer registration in England, on behalf of the Department of Health. There is variation in data quality and not all registries are currently using electronic approaches to data collection.

6.27 The government will set out its plan to strengthen cancer registries, taking account of the Gillis review, in autumn 2000.

Action and Milestones

2000

  • All Regional Offices to set up Regional Cancer Steering Groups

2001

  • All cancer networks to assess local services against national standards as basis for peer review visits
  • All Regional Offices to begin peer review visits All health authorities to take full account of NICE recommendations on cancer drugs
  • National minimum data sets for breast, colorectal, lung and head and neck cancers introduced

2002

  • All health authorities, PCTs and NHS trusts to take full account of NICE guidance on cancer services when published
  • National minimum datasets for all other cancers developed

Access keys