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Developing a core clinical data set for cancer

Margaret P Staples, J Mark Elwood, Alan S Coates and Lizbeth M Kenny
Med J Aust 2003; 178 (2): . || doi: 10.5694/j.1326-5377.2003.tb05083.x
Published online: 20 January 2003

To the Editor: Optimising the management of cancer patients requires objective decisions about "best treatment" strategies, based on high quality data collected systematically from all treated patients (or at least a representative sample of them). Relating treatment and stage at diagnosis to individual outcome can allow monitoring of whether treatment is consistent with best practice, and can provide a systematic foundation for evidence-based care. Clinical cancer data collection also allows treatment services to be evaluated, as institutions can monitor throughput and endpoints. However, institution-based data collections may not be representative of all cancer patients, and aggregation of data from several institutions is needed to obtain a comprehensive picture.




Correspondence: 

  • 1. Coates A. A clinical cancer registration common data set. Melbourne: National Cancer Control Initiative, 1999.
  • 2. NSW clinical cancer data collection for outcomes and quality. Data dictionary. Version 1. Sydney: Public Health Division, NSW Health, 2001.

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