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Improving outcomes for people with skin tumours including melanoma

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<strong>Improving</strong> Outcomes <strong>for</strong><br />

People <strong>with</strong> Skin Tumours<br />

<strong>including</strong> Melanoma<br />

Background<br />

A. Recommendations<br />

It is recommended that the Royal College of Pathologists minimum<br />

dataset [30] is implemented in order to enhance the quality of cancer<br />

registration.<br />

1<br />

It is recommended that at least two cancer registries should receive<br />

additional funding to undertake full registration of <strong>skin</strong> cancers,<br />

<strong>including</strong> the registration of BCCs. Ideally this should include the<br />

registries covering the areas <strong>with</strong> the highest and lowest incidence of<br />

<strong>skin</strong> cancer.<br />

Commissioners should implement the recommendations on <strong>skin</strong><br />

cancer prevention outlined in the Health Development Agency<br />

document titled Cancer prevention: A resource to support local action<br />

in delivering The NHS Cancer Plan [14].<br />

B. Anticipated benefits<br />

Improved data collection on <strong>skin</strong> cancer should produce accurate<br />

population-based in<strong>for</strong>mation on cancer incidence, prevalence, service<br />

utilisation, mortality and survival rates. These data will enhance the<br />

understanding of the epidemiology of <strong>skin</strong> cancer and the ability to<br />

monitor the impact of interventions. Specific benefits are envisaged in<br />

the following areas:<br />

• Prevention. Population-based incidence data are required to<br />

monitor the achievement of targets <strong>for</strong> preventing cancer. This<br />

monitoring will probably be required <strong>for</strong> the next 10–20 years to<br />

see whether the current trend can be reversed.<br />

• Early detection. Population-based data are required to monitor<br />

the effectiveness of early detection and health promotion<br />

programmes.<br />

• <strong>Improving</strong> access to specialist care. Population-based data are<br />

required to monitor intervals between referral and treatment of<br />

cancer patients.<br />

• <strong>Improving</strong> treatment. Treatment patterns need to be monitored<br />

to audit adherence to guidelines, effectiveness of interventions<br />

and <strong>outcomes</strong>. Data from cancer registries can identify the scope<br />

<strong>for</strong> NHS intervention. In<strong>for</strong>mation systems will have to be<br />

developed to support this process, <strong>including</strong> a palliative care<br />

dataset.<br />

26<br />

National Institute <strong>for</strong> Health and Clinical Excellence

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