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Minister says 'no' to cancer drug plea

6:02am Saturday 10th March 2007

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HEALTH Secretary Patricia Hewitt has dashed the hopes of North-East kidney cancer patients desperate for a life-extending drug.

Speaking exclusively to The Northern Echo during a visit to the region, Mrs Hewitt made it clear she would not intervene in the growing row over access to new cancer medicines.

Three North-East patients - Kathleen Devonport, 63, from Chilton, and John Hodgson, 75, from Ferryhill, both County Durham, and Ken Potts, 53, from Blyth, Northumberland - have been told by their NHS consultants that a new drug called Sutent is the last option to extend their lives.

All have advanced kidney cancer and no other treatment is available to stop the disease spreading to other organs.

Despite an explicit recommendation from the UK's leading organisation of kidney cancer experts that Sutent - and a similar drug called Nexavar - should be "routinely available" to patients, Mrs Devonport and Mr Potts have been turned down after applying in writing to their local primary care trusts (PCTs).

Mr Hodgson is planning to write to County Durham PCT requesting Sutent next week.

All of the North-East patients have been told by their NHS doctors that they are unlikely to be prescribed the drug. The only option is to pay - at a cost of more than £30,000 a year.

Yesterday, Mrs Hewitt was handed a copy of a document drawn up by clinicians on the National Renal Cancer Institute's Clinical Studies Group calling for the drugs to be made available to UK patients.

Asked why North-East patients were being denied a licensed drug that is widely available in America and Europe, Mrs Hewitt said: "This is an immensely difficult situation for the patients concerned, and I can well understand their feelings about this.

"But decisions like this have to be made by clinicians, not by politicians.

"Now we have set up Nice (National Institute for Health and Clinical Excellence) which is independent, clinically-led, and it is, I believe, the right body to make decisions on which treatments are both clinically and cost-effective and therefore should be available to all NHS patients."

While Sutent and Nexavar have still not been assessed by Nice, she said the decision whether to make the drug available was being made locally by the North-East Cancer Drugs Network.

Mrs Hewitt, who is understood to have come under considerable political pressure after allowing the new breast cancer drug, Herceptin, to be prescribed on the NHS, said it would be inappropriate to comment where appeals by patients to primary care trusts (PCTs) were pending.

Mrs Devonport met a kidney cancer specialist at a private Bupa hospital in Washington, Wearside, yesterday.

Turned down for Sutent by her PCT last week, Mrs Devonport and her husband, Ray, are now trying to find about £10,000 for the first three months of Sutent or Nexavar.

She said: "The price of the drug is ridiculous. The family are all going to help out, but we might have to remortgage our house. Ordinary people cannot put their hands on £10,000 every three months."

The Health Secretary's stance was criticised by kidney cancer survivor James Whale.

Mr Whale, a former Metro Radio DJ, said: "I am beside myself with rage. Both drugs are one of the biggest steps forward for kidney cancer for years."

Mr Whale, who has set up a website calling for patients to get access to Sutent and Nexavar, said: "It is wrong of her to pass the buck. She is the minister. "If she wanted to make these drugs available, she could do it."

Blyth MP Ronnie Campbell, whose Early-Day Motion on Sutent and Nexavar has attracted the signatures of 20 MPs, said: "A constituent may die because he cannot get a drug that could keep him alive. What is going on here? "The cost is nothing compared to the £69bn they want us to spend on replacing Trident."

Pfizer, which makes Sutent, said more patients in Argentina were getting Sutent than in the UK. It said only about 60 people in the UK were getting the drug.


Your Say YourThe Northern Echo

anne, peterlee says...
11:40am Sat 10 Mar 07

i think it is a disgrace that these people in government can take decisions like this about peoples lives they did not ask to get the illness unlike half the junkies drug addicted thieves who get there methadone or detox programmes paid for

Della, Yorkshire, England says...
1:44pm Sat 10 Mar 07

Interesting isn't it, that these drugs are only being rationed for the English?

Gordon Brown finds the money up for his Scottish constituents - thanks to the generosity of English taxpayers and the barnett formula.

The Welsh get free prescriptions and the price rises over the last few years only applied to the English. They can't afford cancer drugs for the English, but they provide them for the Scots and even free asprins for the Welsh!!

A vote for McLabour is a vote for the approved institutionalised manslaughter of people in England.

3rd class citizen in Britain, EU Region says...
1:50pm Sat 10 Mar 07

You may already be aware that Robert Kilroy Silk, MEP, has submitted a question to the EU Parliament, asking:-

"If the Commission will set up a Commission to investigate the way in which a member state is discriminating against its citizens on the basis of their nationality: namely the UK Government denying, for example, the English equal rights with the Scots and the Welsh in that the English suffering from bone cancer are denied the drug Velcade whereas the Scots receive it free; the English suffering from Alzheimer’s are refused the drugs Aricept, Reminyl and Exelon whereas the Scots are prescribed them free; the English have to pay University tuition fees but the Scots do not; the English who are elderly must pay for residential care yet the Scots do not; and the English pay for NHS prescriptions whereas from April the Welsh will not".

DEMAND THAT YOUR MP SHOWS THEIR SUPPORT FOR THIS BILL

DEMAND AN ENGLISH PARLIAMENT
DEMAND THE ABOLITION OF THE ANTI-ENGLISH BARNETT FORMULA

Norrie Livingstone, Western Australia says...
5:33pm Sat 10 Mar 07

We complain here in Australia about a system that appears to be in crisis from time to time, however reading and hearing from friends and relatives suffering in the UK. We have nothing to complain about. The NHS seems to be in crisis permanently. I would not like to be growing old in the UK under the present system. The Government needs to seriously target massive additional funds for the NHS from the obvious waste in other non essential expenditure. I thought New Labour was in power but I must be mistaken.

E.Justice, Gaeshead England says...
6:41pm Sat 10 Mar 07

Yet again the English are treat like disposable items,how dare they,well they dare do anything to the English.And the Labour will still get voted in ,in the North East,Demand a PARLIAMENT FOR ENGLAND,and see them run!

Maria Tribley, DL5 4SZ says...
8:06pm Sat 10 Mar 07

This is my mam's life they are denying. My mam is the most hardworking, selfless person you could ever meet. To think she has worked hard all of her life to bring up her family, to provide and support us like loving,devoted mothers do to be told that she cannot have a chance of a longer life becasue she is not rich enough to be able to afford £30,000 PER YEAR for medication. Do these people who make these decisions have any idea what affect this has on families? My mam has sufferd with Renal Cell Carcinoma (kidney cancer) for over 7 years (she was 56 when she was diagnosed). She has undergone 2 major operations to remove a kidney and 2 tumors. She fought with a strength that i will never know and throughout these years she has not once complained, never felt sorry for herself or asked why me! She has only thought of her family and how it affects us. So can you imagin how a lady with so much love, and selflessness must be feeling to know that she must now depend on her family to help raise £30,000 PER YEAR to extend her life? I know what she is thinking and my heart breaks for her. Why?Why?Why? WHY test these drugs, pass them and make them available but only if you're rich enough to pay out of your own pocket? Unbelieveable! I can't tell you how desperate our family feel, and i'm sure there are many more just like us. Praying isn't working...............

M Hawkins, Durham says...
8:52pm Sun 11 Mar 07

If Mrs Hewitt the most patronising Health Secretary we have ever had believes that we understand that N.I.C.E. do not do the Governments bidding then she is living in cloud cockoo land.
The setting up of this organisation is just a smoke screen and should be called N.A.S.T.Y. how can they deny anybody a chance of a life enhancing drug, when as pointed out Scotland and Wales are treated differently is beyond belief.
Everybody should lobby their M.P. for a change to this inequitable system that denies the English the same rights as those that have their own Parliaments/Assembly's even though we pay the majority of the bills as we contribute more in Taxation.

Gadgie, Durham says...
8:35am Mon 12 Mar 07

Letters about this medical apartheid have been going into the press for the last two years, and still our English MP's do nothing. They are beyond contempt.The Scottish Parliament can afford to send millions in financial aid to Malawi, but there is no money for desperate people in England.

Della Petch, Yorkshire, England says...
10:10am Mon 12 Mar 07

Maria, my heart goes out to you. I have been speaking out against this discrimination for more than two years now, ever since it came to my attention in May 2005, when English women were being denied breast cancer drugs.
The reason this is happening, is because the Scottish Chancellor will not allow the English NHS the same funding as he gives Scotland, Wales and NI. Literally - an English life have been measured at a lesser value than any other in the UK. This is done via the Barnett Formula and for Wales, the Barnett Plus (they get free prescriptions now).

I would urge all decent people to speak out against this institutionalised manslaughter. All communities in England must join together to fight this discrimination. Please, please show your support by visiting the Justice for England website, which is run by two ordinary English citizens.

A protest at this kind of treatment is being made in London on May 1st. Come along. Carry a placard demanding that a live in England be given equal status to that of Gordon Brown's constituents in Scotland. We must not allow anymore lives to be sacrificed so that Gordon Brown can buy votes in his own country.

No more needless deaths in England. It's got to stop. These cancer patients should not be sentenced to death. Help save their lives by joining us in our first public protest. Make them listen!

Della Petch, Yorkshire, England says...
2:07pm Mon 12 Mar 07

Please sign the petition and pass it on to everyone you know -


http://petitions.pm.gov.uk/Slow-Death/

Kevin, Deal says...
10:15pm Mon 12 Mar 07

These drugs are cost affective in Scotland thanks to the Scottish Chancellor handing over extra funding to his country thanks to the Barnett Forumula but he is happy for English folk to die.

And he aims to be Prime Minister and thanks to devolution in effect First Minister of England, then things will get worse.

What does the Health Secretary do for the people of England and her constituents nothing.

Rose Woodward, says...
1:30pm Tue 13 Mar 07

Can I just clarify a couple of things that have been posted on here regarding the availibity of these two drugs in Scotland compared to England. Both the kidney cancer drugs we are discussing here - Sutent and Nexavar are NOT available in Scotland either. they were turned down by the Scottish Medicines Consortium in November 2006 and February 2007 respectively because and I quote ""The economic case has not been demonstrated.""

Note that in this refusal to give drugs to terminally ill cancer patients the Scottish Board do not say the drugs don't work, we know the DRUGS DO WORK because nearly every senior cancer research specialist and Oncologist in the Country has signed a document to say that they do work.

What we have here is a straight confrontation between the Directors of the PCT's who say the drugs are too expensive and the clinicians and senior doctors who know the drugs work and want them prescribed to help alleviate the medical condition of their patients.

That is the straight forward fact of the matter and PCT Directors who pretend otherwise are simply being economical with the truth!!!!! and we know what that means don't we?

They know that by their refusal to allow this drug they are forcing terminally ill cancer patients into the situation of literally being forced to beg for their life in front of a PCT jury who has already told them once they don't consider their lives are worth saving...

What an appalling thing for one human being to do to another. Especially when one human being is fit, well and no doubt earning a good salary and the other human being is ill, in pain and unable to work because they are terminally ill. I despair sometimes of these poeple, are they so institutionalised that they no longer see this?? Are we seriously saying here that we are prepared to sentance a terminally cancer patient to a premature death because we can't find £25.000 a year. How much is spent by the NHS on external management consultants and the like.

Its immoral and unacceptable to treat people in this way.

Instead of scrabbling around trying to find reasons why patients should not have these drugs, the PCT Directors should be making every effort to get these drugs to the patients in their care as soon as possible.

Show your support to these cancer patients:

http://petitions.pm.gov.uk/kidneycancerRCC/

over 2000 signatures in 5 weeks.

LESLEY WARD, Milton Keynes says...
2:34pm Fri 14 Dec 07

My husband cancer was diagnosed on Sept 14th 07 by accident, our lives have been turned upside down, as the consultant has indicated that the most probable treatment would be one of these drug BUT they are not available to us, we have never asked the state for anything worked all our lives paid into the kitty all our lives and heck the one time we need help desperately to save his life and nobody can help!!!it stinks

Comments are closed on this article.




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