How the UK press published hundreds of fake news stories about cancer drugs

By Jerome Burne

Last week the BMJ published an article warning about the dangers of non-drug CAM treatments for cancer headlined: ‘Is cancer fundraising fuelling quackery? Nothing very unusual about that. As the trustee of a small but perfectly formed charity called Yes To Life that’s devoted to providing information about non-drug cancer treatments, I notice such articles, feel briefly irritated and then usually move on.

But this time I paused because I had just read another article that not only put the whole quackery allegation a new light but calmly revealed that all the UK national press had been engaging in mass Fake News exercise about something called the Cancer Drug Fund. Telling readers the exact opposite of the truth about the safety and effectiveness of the cancer drugs it dished out.

Behind its far more anodyne headline: ‘UK newspaper reporting of the NHS Cancer Drugs Fund, 2010 to 2015: a retrospective media analysis’  was a dynamite report published in the Journal of the Royal Society of Medicine  that should lead to calls for resignations and hearings by the likes of the Commons Public Accounts Committee, although it almost certainly won’t.

It does, however, provide an explanation why the ‘quackery’ accusation gets so much support. If you have been regularly told how effective and a breakthrough the latest cancer drugs are, there is little reason to believe that the likes of vitamins or a change of diet could help. They must be a rip-off. It’s only when the true scale of the problems with the drugs become clear that alternatives can be seen as part of the solution.

Fund has been a 1.4 billion pound disaster

First a bit of background. The Cancer Drug Fund (CDF) was set up by David Cameron’s government in 2010 to make new cancer drugs that had been rejected, or not yet assessed, by NICE, available to patients on the NHS. It was wound up in 2015 and naturally, there was a report, published last year to find out whether this public health initiative, launched without any evidence that it was safe or beneficial, had been worthwhile.

One of its authors was Professor Richard Sullivan, director of the Institute of Cancer Policy at King’s College, London and senior author on recent Royalk Society of Medicine (RSM) article  His 2017 report made it very clear that the Fund had been a disaster. It had spent nearly 1.4 Billion pounds on drugs during the five years it had been operating, for virtually no clinical benefit at all.

As this week’s article says: ‘Many of these drugs did not offer any benefit with respect to prolongation of life or improvement in the quality of life … (there is) …little evidence that patient on the fund benefitted.’

Contrasting the claims of the quackery article with the dismal performance of the CDF is revealing. It  reported that 8 million pounds had been raised on crowd funding sites to help people pay for their treatment for cancer with CAM therapies not available on the NHS.

Cancer Drug Fund and clear signs of quackery

This was warned against for several reasons: that the treatments were not backed by evidence, that they ‘may even do harm’ and that they could be exploiting the people donating money. The worry was that these sites had opened a: ‘lucrative revenue stream for cranks, charlatans and conmen who prey on the vulnerable.’

Exactly the same charges, however, apply to the CDF. ‘Not backed by evidence’: The setting up of the CDF was not supported by any evidence at all. In fact, its basic idea was to reject any evidence that the drugs were not effective or too expensive and pay for patients to get them anyway. That certainly set up a ‘lucrative revenue stream’.

One of the jobs of NICE (National Institute for Health and Care Excellence) is to look at the evidence for the cost-effectiveness and performance of newly licensed drugs to decide if they should be made available on the NHS.

So, the drugs CDF were handing out were ones that had already been rejected as duds or hadn’t yet been assessed. True those not yet assessed would have been licensed by the European Drugs Agency but, as explained below, nearly 50% of the cancer drugs passed by the Agency have no evidence of safety or effectiveness. This may also seem unbelievable but this what an analysis of new drugs by a different team at King’s college discovered last year. (More below)

382 fake news stories on cancer drugs in UK press

After the report on the CDF came out, something remarkable happened – nothing. An authoritative report had found that over a billion pounds had been spent on very expensive cancer drugs for no benefit and yet there was no call for enquiries about who knew what when. Instead,according to the RSM article, the UK press responded by engaging in a massive fake news operation. The coverage of the report by virtually all the national press made it seem as if the CDF had been a great success.

A total of 382 stories were written which took various angles. The top four most commonly used were:

1) The CDF is good but would benefit from being made available in Wales and Scotland not just England. 2) It is good but would benefit from more money. 3) It is good and is helping people .4) It is good but should cover more drugs. Just two of the stories were classified as: The fund is bad because the drugs are ineffective and have nasty side effects.

The study calculated that favourable reports outnumbered the negative three to one, commenting that ‘The drugs lack of effectiveness and range of unpleasant side effects ‘counted for little against human interest stories.’

A possible reason for this misleading and irresponsible coverage is that the CDF was the creation of the press in the first place. Many had run emotive campaigns based around personal stories of patients being denied ‘life saving’ treatment because a certain drug was not recommended by NICE. The government had eventually caved in and set up CDF in direct opposition to NICE which had been created precisely to make such tough decisions.

The assumption behind the both the newspaper coverage and the CDF was that patients should have access to drugs ‘no matter what the cost or the evidence for benefit’. This makes a mockery of claims that these drugs are all carefully tested for safety and effectiveness before being released.

Drugs licensed with no evidence of effectiveness

In fact, it soon turned out that the lack of evidence was even worse than the CDF report had revealed Another study, published a few months later found that the principle of getting drugs out to the public as fast as possible and regardless of cost was also being followed by the EMA (European Medicine’s Agency).

This investigation, published in the BMJ, into the benefits of 48 cancer drugs licensed in Europe and made available in the UK over a four-year period found that over half (57 per cent) entered the market without evidence of benefit on survival or quality of life.

‘These are the outcomes that matter most to patients and their doctors,’ said Dr Huseyin Naci, Assistant Professor in LSE’s Department of Health Policy and one of the authors of the study. ‘It is remarkable that so few cancer drugs enter the European market without any clear data showing they can have these benefits .’

And the drive for rapid licensing, an aim shared by pharmaceutical companies, was not limited to the EU. ‘Our regulatory system is broken,’ Vinay Prasad, Assistant Professor of Medicine at Oregon Health and Sciences University, told the BMJ.  ‘We are approving cancer drugs at a rapid pace, yet few come with good evidence. Their marginal benefits from the rarefied world of randomized trials with selected patients can often be lost when they are used on a much wider range of patients in the real world.’

So it is clear that there is a wide and dangerous gap between the information about cancer drugs put out by virtually the whole press – Guardian and FT two honourable exceptions along with the BBC. This is obviously very favourable to the drugs companies and damaging to patients whose lives and safety the papers claim to champion. But it wasn’t just the press who were acting as cheerleaders for new drugs.

Can we trust cancer charities to tell the truth?

As Professor Sullivan’s current (RSM) report makes clear: ‘Public organisation including the charitable research funders failed to publicise the shortcomings of the CDF.’ The report doesn’t make this point, but it seems to me that this is an even more serious professional failure. These are the bodies staffed by experts who are supposed to know what is going on. They raise millions of pounds a year from the public, so they can ‘beat cancer’. Yet the big charities failed to speak out. Who benefited from that? Not the patients.

It’s difficult to find a clearer description of why were should be concerned about the safety and effectiveness of cancer drugs than the picture painted by the ‘quackery’ article of crowdfunding for CAM treatments.

‘These reports may look like uplifting human interest stories, but they rarely highlight the dubious and pseudoscientific nature of some of the treatments. If the media want to report on medical fundraising stories, they should seek the advice of qualified medical experts.’ Unfortunately, it is difficult to know which medical experts are reliable.


Jerome Burne

Jerome Burne

Jerome Burne is the editor of HealthInsightUK. He is an award-winning journalist who has been specialising in medicine and health for the last 10 years and now works mainly for the Daily Mail. His most recent book “The Hybrid Diet” was written with nutritionist Patrick Holford, published 2018. Award: 2015: Finalist for 'Blogger of the Year' Medical Journalists' Association.


  • You will find the root cause of this problem, in our schools. Or, to be precise, you *won’t* find it, – Philosophy and Rhetoric.

    Current generations know not what or how to think, nor can they express themselves coherently and beyond 140 characters. Hence their inability to discern untruths and mis-information in the media.
    ‘Never let the truth get in the way of a good story!’

  • I fear you are right but fortunately with the accessibility of the internet and such journal as this, good counter arguments exist. This allows us lay individuals with a modicum of sense and independent thought to make our own choices.

    I am not alone in cancelling my rather extreme surgery (a double mastectomy for a stage 3 carcinoma with BCIS) and trying some of the alternative integrated therapies including dietary, detoxification and supplements such as B17 and CBD oil.

    It is early days but time is something that I feel I can afford and to be honest, I have never felt better. However, finding clinical support is not easy and with this it would be so much more reassuring.

  • Coming from the USA I fear that our FDA with its ties to industry
    is guilty perhaps of the same problems as noted above.

    Besides even if a drug is found to have some benefit who in his/her right mind would want a few weeks or months to live burdened by the side effects ( loss of hair, appetite, etc) of drugs approved for Cancer

    Barry Solomon, R.Ph., M.Ed

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