
It's a provisional 'no' from NICE
EDIT 16/05/12 – NICE has now approved this drug. More here.
Today the National Institute of Health and Clinical Excellence – NICE, the body that decides which drugs the NHS should pay for – has given a preliminary ‘thumbs down’ to a new prostate cancer drug, abiraterone (Zytiga), after it failed to agree a pricing scheme with its manufacturer.
As regular readers will remember, we played a key role in this drug’s development, from pioneering lab work, through pre-clinical studies, all the way up to early patient trials.
This is a deeply disappointing and frustrating decision. Since it became available last year, abiraterone has become one of the most requested drugs on the NHS Cancer Drugs Fund. Both patients and doctors alike value the extra months it gives men with their families, if their prostate cancer comes back after chemotherapy.
Chiefly, we’re upset that the healthcare authorities and the drug’s manufacturers, Janssen (part of Johnson & Johnson), can’t agree a fair price for the drug.
We also think there are some issues with NICE’s calculations, which we’ll discuss below.
Thankfully, this decision isn’t final, and can be appealed NICE is now asking for comments through its consultation process. But we’re dismayed that this will mean another long wait of many more months before there’s any hope of progress. And while we wait, there will be men in the UK who will be denied a drug that could help them.
Here’s a video of our chief medical officer, Professor Peter Johnson, explaining what he thinks about the decision:
We need to be clear: abiraterone isn’t a cure for cancer.
But for the thousands of men diagnosed every year with prostate cancer that has spread, it has the potential to ease suffering in the late stages of a terrible disease, and give men more time with their families. The average survival time for these men is just 11 months. Trials have shown that abiraterone could give them an extra four.
Vested interest?
Some will say that we’re only upset because Cancer Research UK stands to earn money from sales of abiraterone. And we do have an interest here: thanks to the way we licensed our initial discoveries to the pharmaceutical industry, we stand to receive royalties from the drug’s sale.
But those funds would be ploughed back into our urgent search for better ways to treat this terrible disease. We receive no government funding for our research – almost all our income comes from the public’s generosity. Things are tight for everyone, and we’re having to seriously prioritise our research funding. Every penny counts.
On top of this, it’s hard to tell our supporters that a drug whose development they helped to fund isn’t going to be available to patients. More recently, to try to prevent this situation arising, we’ve been much more forensic in contracts we sign with the pharma industry, to encourage them to market the resulting drugs at a price suitable for the NHS.
But we signed the original agreement to develop abiraterone in the late 80s, long before NICE was even a twinkle in the Department of Health’s eye.
Our motive is not self-interest. At Cancer Research UK we passionately believe that to help people with the disease, we have to understand what makes cancer tick, and use that knowledge to develop better treatments.
Abiraterone is a shining example of this vision. In the 1990s, we helped fund researchers at The Institute of Cancer Research to identify the molecular machinery that helps prostate cancers use testosterone to grow and spread. They developed chemicals that could interfere with this process. They tested and refined these chemicals into a drug that could make a difference. And they conducted early trials of this drug.
We watched proudly as others at The Institute of Cancer Research, with Janssen’s support, built on that platform, rigorously testing the drug in clinical trials. These trials proved that the drug could improve things for the people who really matter – patients.
So hearing that men are to be denied this drug as a routine choice is a huge let-down, and a real blow to the morale of everyone who shares our dream of conquering cancer through scientific research.
Where did things go wrong?
First, let’s look at NICE’s calculations.
Around 37,000 men are diagnosed with prostate cancer every year in the UK. Of these, about 10,000 are diagnosed with advanced disease.
But abiraterone is only currently intended for men with advanced prostate cancer who have already had chemo, which isn’t suitable for all men. We’ve spoken to a range of experts who agree that the true figure is probably fewer than 7,000 men – and we think this number is low enough for the drug to be assessed under NICE’s end-of-life guidance, which has less-stringent rules over cost.
So we think the overall cost could be more manageable than NICE’s initial calculations appear to have indicated. They disagree with us, and issued a statement to say so. But all the evidence Janssen gave them backs up our point of view; they appear to have dismissed this on the advice of a single expert.
The drug’s high cost is perhaps a more significant factor. We’re well aware that abiraterone is an expensive drug* – it costs about £3,000 for one month’s supply – and we live in straitened times. But the challenges of the current economic climate need to be shared. Janssen have offered the NHS a discount, but clearly not enough. We want them to agree a discount scheme that reflects the current financial constraints on the NHS.
If NICE tweak their sums, and Janssen are willing to compromise, we desperately hope abiraterone will be allowed to enter routine use.
Men in England with advanced prostate cancer can, of course, consider asking their doctor to apply for access to abiraterone through the Cancer Drugs Fund. But this is a finite pot of money that’s only available until 2014. It has to service the needs of patients with many other types of cancer. We mustn’t overload it, or others will suffer.
And crucially, the Fund doesn’t apply to men in Scotland, Wales or Northern Ireland (the Scottish drugs watchdog, the SMC, say they aim to appraise abiraterone by March 12th).
How long will the appeal take?
Appeals need to be submitted NICE want to hear from other experts by February 23rd, and say a final decision should be made by May. And this highlights a wider problem – NICE’s system still appears to be overly reliant on economic, rather than clinical, values. As we discussed in December, the Government is planning to reform drug pricing in the UK, through a proposal called ‘value-based pricing’. We want this new system, however it works, to be faster, more transparent, and focused on delivering positive outcomes for patients.
But that’s for the future. In the here-and-now, we’ll be consulting with our colleagues at other clinical and research organisations. If you have anything you want us to highlight, please leave your thoughts below. As well as people affected by prostate cancer, we’re also keen to hear from the people who look after them – clinicians, nurses, GPs and other carers.
We hope that the appeal is successful, responses to this consultation convince NICE and Janssen that the drug represents a real step forward for men with prostate cancer, so it can be made available on the NHS for those could benefit from it.
Henry
*Edit 03/02 – we’ve added more details about the cost of abiraterone above, in response to a request on Twitter
Edit 06/0 – after discussion with NICE, we have slightly amended the wording of a few points above.
Comments
Stuart Fox February 4, 2012
Ms. Mulhearn states all that is needed to be said.
We are in Country that massively supports overseas aid, whilst their Governments can waste billions on their own fat car lifestyles. We are supposed to be a
‘wealthy’ western Nation!! Don’t make me laugh whilst we have our own people on the poverty line our old folks being denied a decent and honourable later life, and then this utterley indefensible denial of our Cancer sufferers to an extended life. Deplorable!!
and we rely on Charities to fund what the Government should be doing!!
I am utterley sick and tired of this Countrys Government and all it stands for!!
Tony Shaw February 4, 2012
I’m lucky- I was diagnosed with bowel cancer and received the best treatment possible at the William Harvey Hospital in Ashford, Kent. This was 4 years ago, and I feel great. My sympathies go out to those who have been diagnosed with prostate cancer (and their families, too). I couldn’t agree more with the comments made about other government expenditure, and as for the banker’s bonuses…..- words fail me!
Come on, you decision makers, THINK!!
Nikki February 3, 2012
Shame on NICE! They should be officially renamed the National Institute for Cost Effectiveness! Once again they get it wrong. How can any price be put on life?! Too many patients are being denied effective drugs in this country which can extend and give better quality to life and also give others much needed hope. I do so hope NICE and Janssen can work together on a solution so that all patients who need this drug may access and benefit from it as part of their deserved treatment.
Deborah February 3, 2012
My dad died two years ago, he was diagnosed with prostate cancer at 74 and was told he was too old to operate on. Later we found out that the cancer had spread to his bones. He had radiotherapy and drugs. I sat with my dad at his last hospital appointment and my dad begged the doctor to give him something, anything so he could see his grandchildren just a little bit longer. It brings tears to my eyes just thinking about how desperate he was that day. I now worry for my husband, son and son-in-law. Money shouldn’t come into it.
Adi February 3, 2012
I lost my day to prostate cancer 2 years ago and I can’t emphasize enough how important even the hope for this drug was to our family…What I wouldn’t have given to have even one more day with my Dad – it would be so much more that the montly cost and I agree with Bryan -you can’t put a price on the extension of life to those for whom it matters.. who knows, if he’d had the opportunity to have this drug he might even have been walking me down the aisle this May? I will definitely sign the petition on behalf of all those families like mine
Adi Matchan February 3, 2012
As someone who lost my Dad to prostate cancer 2 years ago, I can’t emphasize enough how much it would have meant to extend his like…even by ‘as little’ as 4 months – right now I would give twice the monthly cost to have one more day with him… I agree with Bryan..any life extension is priceless to those affected.. and who knows, maybe he could have even walked me down the aisle this May? I will certainly sign the petition on behalf of all families like mine.
Mick Macauley February 3, 2012
I was diagnosed with Prostate Cancer 10 years ago and there was little in the way of drugs to help. I was 52 years old. As a result I had a radical prostatectomy and later several weeks of radiotherapy. I know it worked and that is wonderful, but a drug trial would also have been a lot less gruelling to start with, it is such a pity that everything to do with living a better life carries such a financial burden. the people that make the decisions really need to look at those that suffer most, these drugs are developed over years and years of work and research, why cant we just be allowed to take them without begging.
strange but they may be NICE by name, but they are not always NICE by nature.
Charles February 3, 2012
For £3,000 a month – I think I will see my days out with cocaine.
Brian Naylor. February 3, 2012
If CRUK are talking about a compromise situation between Janssen and NICE, would it not seem to be that a compromise between CRUK and Janssen on the matter of royalty payments could be a step in the right direction and perhaps lead to a more sensible price structure for this drug,
Peter Dodds February 3, 2012
Right from the days of Avastin, i have been aware of the shenanigins of N.I.C.E. I am sure i am not the only one who wonders what is the point of all these developments when the man or woman in the street cant make use of them. It is like someone putting your favorite meal on the table in front of you and then someone rushing into the room and handcuffing your arms behind the chair. My heart bleeds for all the sufferers out there and who knows it could be my turn next…. or yours ! Still happy days, we will have lots of money to spend on some more wars soon.
Stuart Fox February 3, 2012
Once again the Drug Company ‘Giants’ are peddling their wares at obscene costs.
I am fully aware of research and development costs, but to try it on with the NHS is really despicable. Are those Companys really serious in thinking that the NHS will fund £3,000 per month? per patient?
Let those Companies tout their products elsewhere and find out that their market at this price, even worldwide, will be minimal!!
Robert Maley February 3, 2012
Once again the drug companies are trying to milk the british publc. I appreciate the cost of drug development but surely the cost is way over the top. This will in all probability soar the profits and pockets of the shareholders. While the big companies and millionaires avoid paying or do not pay tax the British public are being denied an important drug, having services cut and seeing privitisation of the NHS by the back door, never mind we are all in this together. Well the working class are paying for it, first things first.
Roy Workman. February 3, 2012
When they decided to name the quango as the ‘National Institute for Health and Clinical Excellence’ – which abbrieviates to NICE, they should have been more truthful and named it ‘National Institute for Controlling Expenditure’ which also abbreviates to NICE.
Graham Barrett February 3, 2012
Strange how billions can be found to build high speed train links that nobody wants, wars, benefits, olympics, etc,etc, but not on really important things like this. Trouble is, I think, not enough polititians have this problem. If they did it might focus their minds a bit more.
Merab Short February 3, 2012
As much money as possible should be spent to help those who need this drug. however, as someone else has commented research to spot it at an earlier stage.Joe public should be able to reap the benefits of his donation and have some say in the rationing of this drug and the distribution of the profits gained.
Malcolm Macey February 3, 2012
It seems cruelly ironic that the biggest contributor to CR UK`s funds,ie.the little man in the street,will once again be theleast able to take advantage of a capable new drug.
BRYAN BALDWIN February 3, 2012
I was diagnosed with stage 4 kidney cancer in 2006. After an appeal I was allowed a drug called sorafinib (Nexavar ) I was told I may get up to 18 months life extention. I am still going 5 1/2 years later. These drugs are expensive but who can put a price on a life. I have been gifted with 3 Grandchildren which I would never had seen had I not have had the drug.Any life extention is priceless as it gives the patient time to say and do the things they probably would not have had.
Anne Scottow February 3, 2012
My husband has been on aberaterone for nearly four weeks and has an appointment next week for a check-up and hopefully will receive a further month’s supply of the tablets if all is well. The difference the drug has made to his symptoms and morale is amazing, even after this short time. We read yesterday’s NICE decision with sinking hearts and wonder whether his treatment will continue. If there is going to be a petition we will certainly sign it. For hope to be snatched away is cruel, for us and for many many others.
T Smith February 3, 2012
“as a tax payer I would be appalled if my taxes were being used to pay for 1 month end of life when there are so many demands on limited health service budget”
I am quite surprised that in a forum like this, you can say something so insensitive – and simplistic. Clearly, some of the health budget must go towards end of life care – after all, we all die. Perhaps when you die, you would like to be alone, with no pain relief or assistance?
How exactly that end of life care is implemented is another matter. Obviously, hard though it is, economical issues have to be balanced with clinical ones in order to best care for the greatest number of people. I am very conflicted on this particular issue: while I understand that the health service is stretched, I know how much an extra couple of months can mean to a family – it is not something you can put a price on. I can only hope that after recalculating, the money can be found somewhere.
Heather Wilkins February 3, 2012
As a retired Macmillan Urology Nurse I am very saddened that this drug is not approved for the men who can benefit from it. It is a sad world where we can spend millions on missiles to destroy life, but a few thousand to improve someone’s quality of life is seemingly out of the question.
Neville Laporte February 3, 2012
My views reflect a lot of what has been said above. If publicly funded CR UK has been a key developer of the drug abiraterone, how does Jannsen justify a cost of 3000 pounds a month. Looks more like making money then saving lives. Though I will continue to contribute, I wish CR would nail down what the eventual outcome and cost of a treatment will be before entering into a deal with drug manufacturer.
John Gordon February 3, 2012
Why are we still giving millions of pounds in aid to other countries such as India who have a space programme and are considering buying fighter jets from overseas, surely we should look after our own first.
Belinda Senior February 3, 2012
I am angered by NICE’s decision. Having lost my step-dad to Prostate cancer 2 years ago and now have a close friend with the decease; it is infuriating that the length and value of someone’s life can be determined by a govt department who are effectively held to ransom by the pharmaceutical company. There are no winners here. Dreadful and upsetting.
mark hughes February 3, 2012
yes its expensive , & i hope the price can & will be brought down, though i think that if itwa sone of theirloved ones or themselves who neede treatingit would be a different matter , its amazing waht we canfind moneyfor though
Dave February 3, 2012
Royalties ploughed back into research is for commercial CRO’s and its how they operate. Charities should research for the benefit of the drug regrdless of any royalties recieved afterall its not CR UK “plc”. There are plenty of drugs that have dual use but are not researched by drug companies because the drug is off-patent and not profitable, this is were the not for profit organisations come in. Adding a commerical interest by way of patent royalties in a charitable organisation is a bad move and that avenue is for the commercial companies to persue. To charge a patient a royalty (in effect as they charge the manufacturer) for a drug that has been developed from donations just doesnt sit well.
yvonne mulhearn February 4, 2012
I cannot believe the priorities of this goverment, they can find billions for foreign aid, millions to send to Poland for child benefit, millions in housing and social security and NHS care for people coming into this country who have never paid a penny into the pot yet they cant pay for a life saving drug for the people of their own country who have paid all their life such as my husband who at 52 has advanced prostate cancer. Luckily for us we have private medical insurance with BUPA who are funding it for him. We have people coming into the country with pre existing diseases and illnesses who are being treated for free, housed for free and educated again for free, it doesnt make sense. Get your act together Mr Cameron and start treating your own people with these terrible illnesses with dignity and the respect they deserve, these are the people who by working all their lifes are helping to fund your foreign aid and treat the foreigners who arrive here, I am disgusted.