Cancer Dataset
"More than one in three people in England will develop Cancer during their lives. One in four will die of it...So better, prevention, detection and treatment of cancer matters to us all"
NHS Cancer Plan
Status
Following the publication of the Cancer Reform Strategy (2007) and review of the current datasets, the Datasets Service is working with the National Cancer Intelligence Network (NCIN) to revise the datasets. This will ensure that the datasets meet the needs of the current service and policy requirements.
A project board has been established to oversee the review of the National Cancer Dataset (see details below). The purpose of the project is for the dataset to be approved as an operational standard for the NHS. The work, commencing in June 2009, includes the necessary elements to support a submission to the Information Standards Board for Health and Social Care (ISB). Approval by the ISB will enable the dataset to be mandated as a collection in the NHS. This will be notified to the NHS and system suppliers via the publication of a Dataset Change Notice (DSCN).
It is anticipated that the project will complete its work in April 2012, with dataset collection being mandatory from September 2012.
Background
The National Cancer Dataset (NCDS) "core" was approved in December 2002 as a Strategic Standard (now classed as a Fundamental Standard). The approval of this "core" Dataset was followed by the approval of the appendices for Lung, Breast, Head & Neck, Colorectal, Upper GI, Gynaecology, Skin, Brain, Sarcoma and Urology. The requirments for surgical Voice Restoration, Haematology and Thyroid appendices were also approved by ISB.
The National Cancer Plan was published by the Department of Health in September 2000 and presents the government's strategy for investment and reform across the NHS, giving cancer services high priority.
NCIN are continuing with the project to review the National Cancer Dataset to ensure that the collection is up to date and meets current service and policy requirements. The project team is working with the 12 NCIN Site Specific Clinical Reference Groups to review the requirements of the collection. This project work will also include reviewing the cancer registration dataset. The data items identified by the NCIN Site Specific Clinical Reference Groups and the reviewed cancer registration dataset will be collated into one dataset which will be taken forward for approval as an NHS information standard. In order to get this approval, the dataset will be subject to operational testing to prove that it can be collected.
Project documentation
For further documentation related to this Project and to access the existing National Cancer Dataset reference documents, please go to the document dowloads page.
Key personnel
- Project Executive: Chris Carrigan, NCIN
- User Representatives:
- Jennifer Benjamin, Department of Health
- Kath Nuttall, Lancashire & South Cumbria Cancer Network
- Mick Peake Clinical Lead, NCIN
- Di Riley, NCIN
- Jem Rashbass, Eastern Cancer Registry & Intelligence Centre