Two breakthrough Alzheimer's drugs have been deemed far too expensive, for too little benefit, to be offered on the NHS. The medicines are the first to slow the disease, which may give people extra time living independently. The National Institute for Health and Care Excellence (NICE) concluded they were a poor use of taxpayers' money and said funding them could lead to other services being cut. Campaigners say it is a disappointment, but dementia experts have also supported the decision. The two drugs, donanemab and lecanemab, both help the body clear a gungy protein that builds up in the brains of people with Alzheimer's disease. The medicines do not reverse or even stop the disease, rather brain power is lost more slowly with treatment. Clinical trials of these drugs were celebrated as a scientific triumph as they showed, for the first time, it was possible to change the course of Alzheimer's. But since then a row has developed over the cost of the drugs and how meaningful the benefit is. The official price in the US is £20,000-£25,000 per patient per year. What the NHS would pay is confidential. Around 70,000 people in England with mild dementia would have been eligible, potentially putting the bill in the region of £1.5bn a year for the drugs alone. NHS resources, including regularly infusing the drugs directly into spinal fluid and frequent brain scans to manage dangerous side effects, would also massively ramp up the cost. The benefit of the drugs is also debated. They potentially delay the transition from mild to moderate dementia by four-to-six months. That could mean more time without needing daily care, driving, being present for significant family events and socialising. But Prof Rob Howard, from University College London, said real-world benefits "were too small to be noticeable". In trials of lecanemab, patients were better off by 0.45 points, on an 18-point scale ranging from healthy to severe dementia. Yet he said the cost would "have been close to the cost of a nurse's salary for each treated patient". The decision not to fund the drugs is not a surprise. The first assessment last year concluded they were not cost-effective. Helen Knight, director of medicines evaluation at NICE, acknowledged the latest news would be "disappointing" but said the benefits were "modest" at best while requiring "substantial resources". "If they were approved they could displace other essential treatments and services that deliver significant benefits to patients," she said. NICE said its appraisal had factored in potential savings in the cost of providing care, but the drugs were still deemed unaffordable. NICE decisions apply to the NHS in England, but are normally adopted by Wales and Northern Ireland too. Scotland has its own method for approving drugs. The pharmaceutical companies have three weeks to raise concerns about how the review was performed, otherwise the decision becomes final on 23 July. Both pharmaceutical companies involved, Eisai for lecanemab and Eli Lilly for donanemab, say they will appeal against the decision. Nick Burgin, from Eisai said the NHS "is not ready" for the challenge of tackling Alzheimer's and flaws in the process meant their drug would have been rejected "even if Eisai provided lecanemab to the NHS for free". Eli Lilly, the company behind donanemab, has already expressed its disappointment. "If the system can't deliver scientific firsts to NHS patients, it is broken," said Chris Stokes, Eli Lilly's president and general manager of UK and Northern Europe. The sentiment was echoed by both the Alzheimer's charities. Prof Fiona Carragher, from the Alzheimer's Society said "the science is flying but the system is failing" and it was "highly disappointing" the drugs were not available on the NHS. Hilary Evans-Newton, the chief executive at Alzheimer's Research UK, said the result was "painful" and patients will miss out on this and future innovations "not because science is failing, but because the system is". However, others say NICE has made the right call. Tom Dening, professor of dementia research at the University of Nottingham, said he was "in complete support" as the benefits of the drugs were "minimal" and a "distraction" from the real issues in dementia. "[Namely the] unglamorous challenge of providing people with dementia and their families with activities, care and support that we already know are beneficial for their mental and physical health," he said. Prof Atticus Hainsworth, from St George's, University of London, said: "NICE is simply doing its job." Beyond lecanemab and donenamab there are 138 dementia medicines being tested in 182 trials around the world. Prof Tara Spires-Jones, director of the centre for discovery brain sciences at the University of Edinburgh, said: "There is hope for safer, more effective treatments on the horizon."
Alzheimer's drugs that slow the disease will not be made available on the NHS
TruthLens AI Suggested Headline:
"NICE Declines Funding for Alzheimer's Drugs Donanemab and Lecanemab Due to Cost Concerns"
TruthLens AI Summary
The National Institute for Health and Care Excellence (NICE) has announced that two groundbreaking Alzheimer's drugs, donanemab and lecanemab, will not be made available on the National Health Service (NHS) due to their high costs and limited benefits. Both drugs are designed to slow the progression of Alzheimer's disease by helping the body eliminate a harmful protein that accumulates in the brains of affected individuals. While clinical trials have indicated that these medications can delay the transition from mild to moderate dementia by approximately four to six months, the NHS has determined that the financial burden of funding these drugs could reach an estimated £1.5 billion annually for around 70,000 eligible patients. NICE concluded that the potential benefits do not justify the extensive resources required for treatment, including regular spinal infusions and frequent brain scans, raising concerns about the impact on other essential health services funded by taxpayers' money.
Experts in dementia care and research have expressed mixed reactions to the decision. While campaigners and pharmaceutical companies have criticized the ruling, arguing that it deprives patients of crucial innovations, some dementia specialists support NICE's assessment, suggesting that the actual benefits of the drugs are minimal. For instance, one expert noted that the improvement observed in clinical trials was only 0.45 points on an 18-point scale measuring dementia severity, a change that may not be significant in practical terms. As a result, NICE's conclusion aligns with a previous assessment that deemed the drugs not cost-effective. The pharmaceutical companies involved have indicated plans to appeal this decision, asserting that the current system is inadequate for addressing the challenges posed by Alzheimer's disease. Meanwhile, the search for more effective treatments continues, with numerous other dementia medications currently undergoing trials worldwide, suggesting that hope remains for future advancements in Alzheimer's care.
TruthLens AI Analysis
You need to be a member to generate the AI analysis for this article.
Log In to Generate AnalysisNot a member yet? Register for free.