Petition The Cancer Drug Fund (CDF) is not fit for purpose and needs to be replaced

The Government recognises the importance of having access to new and promising treatments for people affected by cancer and firmly believes that clinically appropriate drugs that are established as cost-effective should be routinely available to NHS patients. This year £340 million has been invested in the Cancer Drugs Fund (CDF) and 72,000 people in England have so far received the life-extending cancer drugs that would not otherwise have been routinely available to them.

NHS England is responsible for the operational management of the Fund.
Advances in medical science mean that new cancer medicines are emerging all the time and NHS England needs to regularly prioritise its national CDF list.

Decisions on which treatments are included on the national CDF list are made by the CDF expert clinical panel because it is right these decisions are clinically led.
The panel includes expert oncologists, oncology pharmacists and patient representatives.

Where a drug has been removed from the national CDF list as a result of the re-prioritisation process, any patients currently receiving the treatment under the CDF will continue treatment until they and their clinician consider it appropriate to stop. In addition, clinicians can make Individual Cancer Drug Funding Requests (ICDFRs) on the grounds of clinical exceptionality.

NHS England is currently considering proposals for evolving the CDF in a more sustainable way. At its meeting on 23 July 2015, the NHS England Board set out proposals for the Fund and agreed that any proposals should be subject to public consultation later in the year.

More generally, the Government takes the issue of ensuring rapid access to innovative therapies very seriously, which is why it has launched an Accelerated Access Review, independently led by Sir Hugh Taylor, to make recommendations to Government on speeding up access for NHS patients to innovative and cost effective new technologies.

The aim of the review is to ensure that the UK is the fastest place in the world for the design, development and widespread adoption of medical innovations so that innovative medicines, devices, diagnostics and digital products get to NHS patients as quickly and safely as possible.

The Review will make recommendations to Government by the Spring of 2016 and an interim report will be published later in the Autumn. More information can be found on the Government website at www.gov.uk by searching for ‘accelerated access review’.

Department of Health