Brain Tumour Survival Rates Debate
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Main Page: Susan Murray (Liberal Democrat - Mid Dunbartonshire)Department Debates - View all Susan Murray's debates with the Department of Health and Social Care
(1 week, 4 days ago)
Commons Chamber
Susan Murray (Mid Dunbartonshire) (LD)
I thank the hon. Member for Mitcham and Morden (Dame Siobhain McDonagh) and my hon. Friend the Member for Witney (Charlie Maynard) for securing this important debate. I am here speaking tonight on behalf of my friend George, who is now in his eighties and still fundraising for research into brain tumours in the name of his son, David, who he lost far too soon.
Brain tumours remain one of the clearest examples of a condition where outcomes have not improved quickly enough. They are the biggest cancer killer of people under 40 in the UK. Each year, more than 12,000 people are diagnosed with a brain tumour and only a quarter of adults with a primary brain cancer survive for five years after diagnosis.
That reality is compounded by late diagnosis. Studies have shown that around 45% of brain tumours are diagnosed in an emergency setting—far higher than for other cancers—meaning too many people start their treatment far later than they should. That is why I support calls for a national cancer plan to increase survival rates of those diagnosed with brain tumours.
We have national campaigns to spread information on bowel cancer and other types of cancer to raise awareness, and a campaign would allow people to spot the early signs of brain tumours, but awareness on its own is not enough, as we have been hearing. Earlier recognition has to be matched by specialist services that can respond quickly and consistently.
Health and social care are devolved, but brain tumour patients should not find that their chance of being offered a trial or the speed of a referral depends on the nation in which they live. I would therefore like to urge the Government to work with the Scottish Government and other devolved Administrations on a joint approach, with research supported properly across the UK and funding used as effectively as possible.
This is about improving outcomes and ensuring fair access. It requires co-operation between the UK Government, the devolved Administrations and research institutions. Research is essential to saving lives and it relies on the co-operation, shared strategy and consistent support for trials. A disjointed approach without co-ordination slows the innovation that is possible. That is a failure not just for researchers, but for patients and the families of those affected. A national strategy is needed to push for awareness to facilitate co-ordination and, most importantly, to save lives.