Achieving World-Class Cancer Outcomes A Strategy for England

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Presentation transcript:

Achieving World-Class Cancer Outcomes A Strategy for England 2015-2020 A very brief overview for the Gynaecology SSG Provided by Emma Pugh Cancer Manager - WAHT

Achieving World-Class Cancer Outcomes What is it? What does it say? What should we do? 18/11/2018 Presentation for Sarcoma - SSG 8Sept15

Presentation for Sarcoma - SSG 8Sept15 What is it? An Independent Cancer Taskforce was established in January 2015 by NHS England on behalf of the Care Quality Commission, Health Education England, Monitor, National Institute for Health and Care Excellent, Public Health England and the Trust Development Authority to help develop a five-year strategy for cancer services. Aim was to improve survival rates and save thousands of lives. The report was informed by responses to a Call for Evidence. Nearly 100 workshops and meetings were held, involving around 600 participants, the proactive involvement of patients, consultation with around 30 cancer charities, and professional groups. The Independent Cancer Taskforce published the strategy on 19th July 2015 18/11/2018 Presentation for Sarcoma - SSG 8Sept15

What does it say? Six strategic priorities 18/11/2018 Upgrade in prevention and public health Achieve earlier diagnosis Patient experience on a par Support for living with and beyond cancer Investment to deliver modern high-quality service Overhaul for commissioning, accountability & provision Outlines how an additional 30,000 patients every year could survive cancer for 10 years or more by 2020 (11,000 through earlier diagnosis). 18/11/2018 Presentation for Sarcoma - SSG 8Sept15

Presentation for Sarcoma - SSG 8Sept15 What does it say? A radical upgrade in prevention and public health. The strategy outlines how the NHS should work with the Government to improve public health, including adopting a new tobacco control strategy within the next 12 months, and a national action plan on obesity. The Taskforce wants to see a reduction in smoking from 18.4 per cent now, to less than 13 per cent by 2020. A national ambition to achieve earlier diagnosis. The ambition set out is that, by 2020, 95 per cent of patients referred for testing by a GP are definitively diagnosed with cancer, or cancer is ruled out, and that patients get this result within four weeks. This requires a significant increase in diagnostic capacity, giving GPs direct access to key investigative tests, and the testing of new models which could reduce the burden and reliance on GPs. Currently, patients urgently referred for suspected cancer by their GP need to be seen by a specialist within 14 days of referral, but no guidance exists for when patients can expect to get the results. Patient experience on a par with clinical effectiveness and safety. The strategy recommends giving all consenting patients electronic access to all test results and other communications involving further care by 2020. Patients should also have access to a clinical nurse specialist or other key worker to help coordinate their care. The NHS must continue to develop and adopt meaningful ways to measure a patient’s experience, including the annual Cancer Patient Experience Survey. 18/11/2018 Presentation for Sarcoma - SSG 8Sept15

Presentation for Sarcoma - SSG 8Sept15 What does it say? Transformation in support for people living with and beyond cancer. By 2020 every person with cancer should have access to elements of a ‘Recovery Package’ – a comprehensive plan that outlines treatment as well as post-treatment support and care. A national quality of life metric should be developed by 2017 to ensure better support for people after treatment has ended. Clinical Commissioning Groups (CCGs) must ensure they commission appropriate End of Life care, in accordance with NICE guidelines and the Choice Review. Investment to deliver a modern high-quality service, including: o A replacement plan for radiotherapy machines (linacs) as they reach 10-years and upgrading of existing linacs by the time they have been operational for six years; o A permanent and sustainable model for the Cancer Drugs Fund to help patients get access to innovative cancer treatments; o A nationally-commissioned, regionally-delivered, molecular diagnostics service, to guide more personalised prevention, screening and treatment; o Plans to address critical deficits in the cancer workforce. Overhauled processes for commissioning, accountability and provision. By 2016, a network of Cancer Alliances should be established across the country. These will bring together key partners at a local level, including patients. The Alliances would use a dashboard of key metrics to address variation and support service redesign. The Taskforce has recommended that a National Cancer Team (NCT) should oversee the delivery of the Strategy. 18/11/2018 Presentation for Sarcoma - SSG 8Sept15

Presentation for Sarcoma - SSG 8Sept15 What should we do? Review of each priority – what are we doing to deliver this? Well-being events, eHNAs How does this fit along side other local, network activities? Review of diagnostic capacity Review of pathways alongside new NICE guidance “Use” strategy as a lever for change? 18/11/2018 Presentation for Sarcoma - SSG 8Sept15