NHS Cancer Services

John Baron Excerpts

Friday 14th September 2012 Commons Chamber

[Mr John Baron (Basildon and Billericay) (Con)]

May I start this important debate by congratulating the Under-Secretary of State for Health, my hon. Friend the Member for Broxtowe (Anna Soubry), on her appointment to what many of us consider to be an important position in Government? May I also pay a warm tribute to her predecessor, the right hon. Member for Sutton and Cheam (Paul Burstow), who did an excellent job in understanding the issues and pushing the case for cancer care? We wish him well for the future. The all-party group on cancer, of which I am chair, looks forward to enjoying the same constructive relationship with this Minister. However, I secured today’s debate because we believe that after making excellent progress on cancer care the Government now risk making a gross error, which could be very costly indeed, when it comes to cancer treatment.

As the Minister is new in her post, I will, if I may, briefly provide some background information. Cancer survival rates have steadily improved over the past 40 years, but they still lag considerably behind those in Europe and in other countries. Comparisons are never easy, but although we compare with, say, France when it comes to the four or five cancer centres of excellence, it is generally accepted that we lag behind the rest of Europe. The Government have recognised and accepted that point. In January last year, they set themselves the target of saving an additional 5,000 lives by 2014-15, but that would bring us up only to the European average, not even the best.

Why do we in this country trail behind the rest of Europe when it comes to cancer survival rates? In 2009, the all-party group undertook a major inquiry into cancer inequalities that looked at that very issue. What we found was most revealing. We discovered that patients in this country who make it to the one-year survival point stand as much chance as anybody on the continent of making it to five years. Where we fall down badly is in getting patients to the one-year survival point. That led to the conclusion, which is backed up by lots of evidence from those working in the NHS, that the NHS is as good as any other health care system at treating cancer once it is detected, but very poor at detecting it in the first place. It is a national disgrace that nearly one quarter of all cancers in this country are detected only at A and E. That is far too late and it obviously affects survival rates.

The Minister will be fully aware that very rarely in life is there a golden key—an Act or policy through which one can find unbounded riches. However, when it comes to cancer, I would suggest to her that there is a golden key—earlier diagnosis. The earlier a cancer is detected, the greater the chance of survival and the better the survival rate.

Our key recommendation from the 2009 report was the introduction of a one-year survival outcome measure, in order to get the local NHS to raise its game. There is no point in the Department of Health trying to micro-manage primary care trusts; it is better to put up in lights the one-year and five-year outcome measures and to get the local NHS to introduce the various measures and initiatives needed to encourage earlier diagnosis. Those measures could involve greater awareness, earlier or better screening, better use of diagnostics or a combination of those. We should leave it to the local PCTs, while encouraging them to put up in lights the one-year and five-year outcome measures. Such initiatives at ground level would encourage earlier diagnosis, which would result in better one-year and five-year survival rates.

The all-party group campaigned hard on this issue. We raised it in Parliament and at our annual Britain Against Cancer conference—which is the largest of its kind and which is often addressed by Secretaries of State—and elsewhere. We had some success. We were pleased to see the inclusion of one-year and five-year cancer survival rates for breast, lung and colorectal cancer as indicators in the national outcomes framework, which, as the Minister knows, holds the NHS Commissioning Board to account.

Of the two big ideas in the Government’s NHS reforms—the focus on outcomes and the restructuring of the commissioning arrangements—we always thought that the focus on outcomes was by far the most important. We believed that the heat, rather than light, generated by the debate on commissioning structures was unfortunate, to say the least.

In many respects, the national picture has been taken care of. We have the one-year and five-year figures in the NHS outcomes framework, which holds the NHS Commissioning Board to account. Locally, however, it is the clinical commissioning groups—the CCGs—that will play a key role in delivering better cancer care. They are held to account by a different outcomes framework: the commissioning outcomes framework, known as the COF.

The COF will do much to set cancer priorities locally, and it is therefore vital that we get this right. Up until last month, we were led to believe that the five-year survival indicator was to be included in the COF, and the all-party group was lobbying hard to get the one-year indicator included as well. After all, both derive from the same data set. We fully participated in the National Institute for Health and Clinical Excellence consultation in February this year. We learned last month, however, that the NICE COF advisory committee had decided not to recommend the inclusion of either the one-year or the five-year survival rates in the first iteration of the COF. Instead, only the under-75 mortality rates were recommended for inclusion.

I suggest to the Minister that that is a major error. Given all the evidence on how the measure of the one-year and five-year survival rates encourages earlier diagnosis, the Government should not allow this major step backwards in cancer care. The NHS Commissioning Board is, at this very moment, deciding on the make-up of the COF, and the all-party group is calling on it and the Government to include the one-year and five-year cancer measures in this important outcomes framework.

NICE offered two reasons for the exclusion, but they simply do not stack up. First, it said that survival rates were dependent on the socio-economic status of an area. However, the all-party group has heard from a broad range of experts working in the NHS that the most effective way to incentivise early diagnosis is to measure the NHS against cancer survival rates, specifically at one year. The inclusion of cancer survival indicators in the COF is the best way of guaranteeing that CCGs prioritise early diagnosis.

NICE’s second objection related to the application of survival data at local level. However, my understanding, from conversations with the National Cancer Intelligence Network and others, is that cancer survival figures for CCGs can be produced—sliced up, if you like—once the boundaries are known. At the very least, CCGs could then be measured against one-year and five-year survival rates for breast, lung and colorectal cancer, and so be included in the 2013-14 COF, thereby bringing it in line with the NHS outcomes framework.

In our opinion, it is vital that survival indicators are included in the COF, but the all-party-group has also called for proxy measures such as staging and cancer-diagnosed A and E admissions to be included in the COF to complement the one and five-year figures. We have been calling for this because of the smaller population sizes of CCGs compared to what they are replacing—the PCTs. Proxy measures would help to provide a more complete picture of what is happening on the ground, and would help commissioners to identify the bottlenecks to early diagnosis. Will the Minister update us on the progress made on these proxy measures?

Before I conclude and while I have the Minister’s ear, let me quickly raise two further points. Although perhaps a little less urgently than in respect of our main concerns about the COF, the all-party group would like to see both the outcomes framework and the COF to include all cancers. In our view, if all cancer patients are to benefit from the Government’s correct focus on outcomes, it is vital that the rarer cancers be included, thereby narrowing the unacceptable survival gap between the rarer and more common cancers. After all, breast, lung and colorectal cancers account for only 40% of all new cancers. I add that we are somewhat concerned about Government talk about a composite cancer benchmark or indicator because we fear that such a composite would hide failings perhaps in respect of rarer cancers by focusing on improvements made in the more common cancers. We need to narrow that unacceptable survival gap between rarer and the more common cancers.

[Naomi Long (Belfast East) (Alliance)]

I join the hon. Gentleman in welcoming the Under-Secretary of State for Health, the hon. Member for Broxtowe (Anna Soubry) to her new role.

One way of treating more difficult cancers can be the use of very specialist radiotherapy techniques. I have spoken before about stereotactic body radiation therapy and other treatments, which have the potential to improve outcomes, but because they are novel treatments they are advised for use only in clinical trials. Many health trusts are afraid to refer patients because there is no clinical evidence that they are successful for particular cancers. There is a vicious circle here, which needs to be broken so that rarer and harder-to-treat cancers can be treated, at least at that test phase.

[Mr Baron]

The hon. Lady raises a very good point. I believe that cancer networks have a particularly important role when it comes to treatments that span CCGs such as radiotherapy. I know that local cancer networks would help to look into those treatments in order to address the concerns the hon. Lady has rightly raised.

Let me touch briefly on the second point, which is the importance of improving the patient experience. The all-party group recommends that the national cancer patient experience survey should be conducted annually and should be included as an indicator in domain 4 of both the NHS outcomes framework and the COF, as we believe that that would be a solid way of getting the NHS to focus on the importance of improving cancer patients’ experience at all levels.

In conclusion, important though those last two points are, let me return to the central concern of the all-party group and the point of this debate. We think it a very bad decision to exclude the one-year and five-year survival indicators from the COF, and we ask the Government to think again. It sends out the wrong message, defies all the evidence and risks different parts of the NHS focusing on different messages—the outcomes framework on the one hand and the COF on the other. If one thinks about it, there is no reason why the one and five-year measures cannot appear in the COF if they are in the outcomes framework; the numbers can be sliced once the boundaries are known.

Our message is clear: we risk a major traffic accident here, which really could set back cancer care and treatment in this country. We raised this issue with Ministers outside this place prior to the reshuffle, and we raise it again with the Minister in this Chamber now. We urge the Government to think again. A lot of cancer patients are watching this space very closely.

[The Parliamentary Under-Secretary of State for Health (Anna Soubry)]

I congratulate my hon. Friend the Member for Basildon and Billericay (Mr Baron) on securing the debate. I am aware of the excellent work that he has done with the all-party parliamentary group and with cancer charities to promote the inclusion of relevant cancer indicators in the NHS, public health and commissioning outcomes frameworks.

As you will know, Mr Deputy Speaker, there is a lot of terminology in the Department of Health—to which I am very pleased to have been appointed—and I apologise at the outset for any jargon that is used. One thing is certain: my hon. Friend will be more than familiar with it. However, I hope to explain the position in as much plain language as possible.

I am fully aware of the frustration felt by my hon. Friend, his all-party group and the cancer charities over the recommendations from the National Institute for Health and Clinical Excellence about the indicators for the commissioning outcomes framework and the difficulties that are likely to occur in 2013-14, but I can assure him that a methodology for possible one-year and five-year survival rate indicators for potential inclusion in COF is under way. I hope he will accept that that is good news, as is the fact that work is also under way to investigate composite cancer survival indicators at both national and clinical commissioning group level. I will say more about that, but I wanted to begin by reassuring my hon. Friend that we had taken his previous points fully on board.

As my hon. Friend knows, the Government published “Improving Outcomes: A Strategy for Cancer” in 2011. It set out our ambition to halve the gap between England’s survival rates and those of the best in Europe. My hon. Friend spoke of the disappointment that many people feel about our survival rates, and said that everyone wanted them to improve. It is estimated that halving that gap would save 5,000 more lives every year by 2014-15. The strategy is intended to reflect the importance of improving outcomes through the five domains—or areas, as I would call them—of the NHS outcomes framework: preventing people from dying prematurely, improving the quality of life for people with long-term conditions, helping people to recover from illness or injury, ensuring that people have a positive experience of care, and treating and caring for people in a safe environment and protecting them from avoidable harm.

In recognition of the fact that cancer is a big killer—more than 130,000 people die of the disease each year—we have included seven cancer indicators in domain 1 of the NHS outcomes framework. They cover the under-75 mortality rate from cancer and one and five-year survival rates for three major cancer killers, namely colorectal, breast and lung cancer. In addition, two overarching indicators will include cancer data: potential years of life lost from causes considered amenable to health care, and life expectancy at 75.

My hon. Friend has urged us previously to consider other indicators that would reflect improvements in survival rates for rarer cancers, and he mentioned them again today. I can confirm that we have asked the London School of Hygiene and Tropical Medicine to develop composite indicators that might allow improvements in survival rates across all cancers to be assessed. We hope to be able to make a decision in time for the NHS outcomes framework for 2013-14, which is due to be published later in the autumn.

[Mr Baron]

I am heartened by what the Minister is saying, but does she appreciate our view that a composite index should complement the one and five-year survival indicators rather than replace them? We fear that a composite index will mask bad news on rarer cancers with improvements on the more common cancers, which would have greater force in the index because they are more numerous.

[Anna Soubry]

I thank my hon. Friend for making that point, and I certainly take it on board. If there is anything that I am not able to cover in the short time that is available to me today, we will write to him; and, as he knows, my door is always open so that we can continue the debate. It is important, and it is especially important that we do things right.

The NHS Commissioning Board will translate the national outcomes goals for the NHS into measures that are meaningful at a local level in the commissioning outcomes framework. The board authority is now working with clinical commissioning groups and other stakeholder organisations to discuss the shape of the commissioning outcomes framework for 2013-14 and beyond. COF will play an important role in driving up quality in the new system. Covering £60 billion in services commissioned by CCGs across the NHS, it will translate the NHS outcomes framework into clear, comparative data on the quality of services that CCGs commission for their local populations and the outcomes achieved for patients.

Concerns have been expressed that the NICE COF advisory group recommended only one indicator for inclusion in COF and, in particular, that the group recommended no survival rate indicators. NICE’s advisory group is independent of both the Department and the NHS Commissioning Board. NICE was asked to give advice on potential measures to include in the framework, based on the best available evidence. It is now for the NHS Commissioning Board to decide on its final shape for 2013-14.

The NHS Health and Social Care Information Centre has been asked to work with the London School of Hygiene and Tropical Medicine and the Office for National Statistics to develop a methodology for one-year and five-year survival rate indicators for potential inclusion in COF. These will be composite indicators, because of the difficulties associated with getting statistically valid indicators for individual cancers at CCG level.

[Mr Baron]

The national one-year and five-year figures for the three main cancers have been calculated. They must have been drawn from local figures. Experts in this area tell me that once the boundaries are known, it should be possible to slice those figures to show the one-year and five-year picture at a local level.

[Anna Soubry]

The difficulty is that the numbers in each CCG might be very small indeed, and therefore the statistical benefit will be limited. It may well be possible to look at the situation in respect of the health and well-being boards, however; we might be able to look at this at a local authority level.

[Mr Baron]

The Minister is being very generous in giving way, and one of the purposes of Adjournment debates is to enable us to have a bit of a discussion. I take on board her point, but the CCGs are larger than was originally estimated. I would also say that we have suggested the use of proxy measures such as staging and accident and emergency admissions figures to complement, but not replace, the one-year and five-year figures, because they would give a more complete picture at the local level.

Business of the House

John Baron Excerpts

Thursday 6th September 2012 Commons Chamber

[Mr Lansley]

In terms of business, the hon. Lady is right. The House had an opportunity to debate Atos Healthcare, and I think that she may have received replies from the then Minister of State, my right hon. Friend the Member for Epsom and Ewell (Chris Grayling). I personally know that the work done as a consequence of the Harrington reviews, and what we announced in July about the recording of tribunal judges’ reasons for overturning decisions on appeal, will enable us continuously to improve the process.

[Mr John Baron (Basildon and Billericay) (Con)]

I welcome the Leader of the House to his new post. May I ask him to consider one further fact relating to the 2nd Battalion the Royal Regiment of Fusiliers? It is the only infantry battalion that is being axed for political rather than military reasons, in order to save the more poorly recruited Scottish battalions ahead of the referendum. In fact, no Scottish battalions are being axed. I am married to a Scot and I believe in the Union, but discriminating against the English is not the way for us to achieve our goal.

[Mr Lansley]

My hon. Friend had an opportunity to raise that with the Prime Minister at Prime Minister’s Question Time, and I hope that he will take the opportunity that the Prime Minister gave him to make his points at a meeting. However, I do not recognise his description of the way in which decisions were made. They were made on the basis of an assessment of how the armed services could be sustainable for the future, and could secure representation and maintain recruitment throughout the United Kingdom.

Cancer Treatments

John Baron Excerpts

Tuesday 19th June 2012 Westminster Hall

[Mr John Baron (Basildon and Billericay) (Con)]

I congratulate my hon. Friend the Member for Southport (John Pugh) on securing this important debate. The all-party group on cancer, of which I am chairman, has consistently called for us to see the NHS reforms as an opportunity to improve outcomes for cancer patients, and I welcome the chance to highlight that once again.

Perhaps I should start by briefly taking us back to 2009, when the all-party group produced its report on reducing health inequalities. After a long evidence session, with oral as well as written submissions, we discovered that those patients in this country who reached the one-year point stood as much chance of reaching the five-year point as patients in any other country in Europe, but we fell down badly in getting patients to the one-year point. That tended to suggest that the NHS is as good as anybody else at treating patients—once detected—but poor at detecting cancers in the early stages in particular. Other hon. Members have made that point in this debate.

How do we encourage earlier diagnosis? There are few magic keys to solutions in life, but perhaps earlier cancer diagnosis is one of them. The 2009 report concluded that the best way of doing that was to focus on outcomes—to get the NHS actually to look at one and five-year survival rates, because late diagnosis makes for poor outcomes. Getting the local and national NHS to focus on one and five-year rates would encourage the local NHS in particular to drive forward initiatives and earlier diagnosis. We were grateful when the Government accepted the logic of that argument and included one and five-year outcome measures in the NHS outcomes framework. The NHS reforms essentially boiled down to two strands—two initiatives. One was the change in the commissioning structure; the second was the focus on outcomes. For me and for many in the all-party group, the focus on outcomes was by far the most important bit of the NHS reforms.

We welcome the Government’s response so far. The all-party group was pleased that, at the beginning of 2011, the Government released their strategy for cancer, which clearly highlighted the importance that they attached to the issue. They came up with a figure—an ambition—to save an extra 5,000 lives a year from cancer by 2014-15. We should remember that that would take us up to only the European average, not the best in Europe, but it is still a laudable ambition that we very much welcome.

We have had a constructive dialogue with the Government, experts and patients. I want to touch briefly—I am conscious that other hon. Members wish to speak—on some of the key recommendations from the all-party group that flowed from the 2009 report. We welcome the Government’s response to that report. Many others have made the same argument, but we played a small part in moving the Government in the right direction.

However, we are still ambitious with regard to some of our recommendations. For me, the first is key. There seems to be an anomaly in the different outcomes frameworks. We have the commissioning outcomes framework, which has the five-year survival rate as an outcome measure. We have the NHS outcomes framework, which has the one and five-year measures. The COF is the framework by which the clinical commissioning groups will be held to account for their performance, and we are arguing for the one-year measure to be included in the COF, just as the one and five-year measure is included in the national outcomes framework. In other words, we want standardisation.

Our concern is that if we have different outcomes frameworks focusing on slightly different things, or certainly not the same things, a disjointed message can be given. It is important that both the local and the national NHS focus on the same things. I raised that question—the Minister will forgive me for raising it in this debate—in Health questions last week. I was slightly worried about the response. The Minister will correct me if I am wrong, but he cited concerns with the quality of the data available for the one-year measure within the COF. If the one-year data are good enough for the NHS outcomes framework, why are they not good enough for the COF, particularly given that the NHS Commissioning Board will shortly provide geographic boundary data for the clinical commissioning groups? It should not be beyond the wit of man to transfer what we have in the NHS outcomes framework across to the COF once those data from the NHS Commissioning Board are available. I am led to believe that there should be no problem at all with how the data are cut. What does the Minister have to say about that?

To pick up the point made earlier by the hon. Member for Ealing, Southall (Mr Sharma), I also want to question the Minister about why we are not expanding the number of cancers in the outcomes framework. I have a little more sympathy with the Minister on the quality of the data on this one. Whereas I cannot understand why the one-year figures, which are in the NHS outcomes framework, are not included in the COF, I have some sympathy because of the quality of the data for expanding the three cancers that are already there. Those three cancers are obviously common cancers. They account for some 40% of all new cancer diagnoses—we are talking about breast, lung and colorectal cancers. The Minister accepts that there can be a disparity in survival rates between the common cancers and the rarer cancers. Our recommendation would in some respects help to close that gap with the more common cancers. Will the Minister address the point that was made earlier and the point that the all-party group has been pushing hard on for some time?

The Minister appreciates that we hon. Members in the all-party group have had a constructive dialogue, which continues, but this debate is too good an opportunity to miss, so I should like to raise some relevant issues in a more public forum. The all-party group has tended to focus on proxy measures. When we had primary care trusts, the one and five-year figures were statistically robust, because the population sizes allowed them to be so. However, we have started tinkering with the commissioning structure—first, general practitioners and fundholders and then clinical commissioning groups—and the population sizes are somewhat smaller. Therefore one and five-year figures, on their own, are not as statistically robust as we should like. That is why we in the all-party group suggested that staging and emergency admissions could be used as proxy measures to complement, rather than replace, the one and five-year figures, for the benefit of the local NHS.

Hon. Members should not forget that this is all about trying to introduce measures that allow the local NHS to focus on outcomes and introduce, through its own initiative, initiatives such as screening, which was mentioned earlier—there are many others—to try to drive forward earlier diagnosis.

In respect of proxy measures, I understand that the public health outcomes framework, published at the beginning of the year, has already identified the importance of staging data. Certainly, that is so with regard to cancers diagnosed at stages one and two. I am not alone in the all-party group in thinking that it is important that those data are shared across the outcomes framework to ensure a coherent approach throughout the NHS. I am interested in what the Minister says about that. Once again, I accept that we have to be reasonable. This is about quality of data. I hope that the Minister accepts that coherence is needed in respect of the frameworks for public health outcomes, NHS outcomes or commissioning outcomes.

If the big picture of what the NHS should focus on in respect of cancer is coherent—whether top-down or bottom-up—we stand a greater chance of achieving our goals. At the moment, there is a risk that we do not have such coherence. I know that the process is at an early stage, but I am interested in hearing the Minister’s response.

Picking up a point that was raised earlier, all hon. Members accept that improving patient experience is important, which is why the all-party group thinks that we need to do more to push on an open door. We recommended that the national cancer patient experience survey should be conducted annually. Although there is a question about feasibility, there is much merit in that suggestion. The survey should also be included in domain 4 of the NHS outcomes framework and the COF, just to ensure that the message, which is that we regard it as important, is clear. Patients can have the best treatment in the world, but unless their experience is good, particularly at a traumatic time when they have cancer, negative experiences can often act as a dampener and can affect recovery rates as well. It is important to recognise that.

I thank my hon. Friend the Member for Southport for securing the debate. The Minister knows that the all-party group is keen on a constructive dialogue—it is ongoing—and I thank him for the meetings that we have had and for the constructive way that he has liaised with us. I apologise to him for making an early exit, because I have to attend a meeting of the Select Committee on Foreign Affairs. However, he should not think that I am not interested in his response: I shall scan Hansard carefully tomorrow morning.

--- Later in debate ---

[Liz Kendall (Leicester West) (Lab)]

I thank all hon. Members who have taken part in this important debate. I congratulate the hon. Member for Southport (John Pugh), hard-working as always, on focusing on the issue.

Several hon. Members talked about the context of the debate and the improvements made over recent years. Several mentioned the research—published, I think, in the British Journal of Cancer—that showed that, over the past 20 or so years, the NHS in England and Wales has achieved the biggest drop in overall cancer deaths among 10 leading countries worldwide. There have also been significant improvements with individual cancers. For example, death rates for breast cancer have fallen by 40% since 1989, virtually closing the gap with other countries such as France. Furthermore, the NHS has done so despite having a smaller budget, which led the British Journal of Cancer to conclude that the NHS had achieved more with proportionately less than in other major developed countries.

It is clear, however, that far more can and must be done to bring cancer outcomes for all cancers and all patients up to the very best standards achieved in other countries. Hon. Members have rightly said that our overall survival rates are still not as good as those in countries such as Canada, Australia, Sweden and Norway and that, although survival rates are good for breast and skin cancer, for example, they are low for lung and pancreatic cancer. I am also particularly concerned about differences in outcomes for people from different minority ethnic groups or from different social and economic backgrounds. As the shadow Minister with responsibility for older people, I am concerned about the worse outcomes for older people in the UK compared with those in other countries, even after we have taken social and economic factors into account—I shall say a bit more about that in a moment.

Hon. Members welcomed the focus in the NHS outcomes framework on one and five-year survival rates but rightly questioned why the three cancers mentioned account for 40% of new cancer diagnoses and asked about the other cancers that could be included. Although survival rates are absolutely vital, other issues need to be addressed to improve the patient experience and the quality of care—in particular, for those who will not survive cancer, at the end of life.

[Mr Edward Leigh in the Chair]

I want to focus my comments on three key areas of care in which we need to improve services: first, early diagnosis and intervention; secondly, tackling treatment variations; and thirdly, ensuring that the patient experience is at the heart of all aspects of cancer care. There is a very important issue about how we prevent cancer from happening in the first place, but I will not focus on that in this debate.

The hon. Member for Basildon and Billericay (Mr Baron) —I pay tribute to the all-party parliamentary group—hit the nail on the head when he said that the survival rates at one year are crucial, and the differences between our survival rates and those in other countries are largest around that first year. We have to ensure either that patients present to their doctors earlier or that we identify them through effective screening. We then have to ensure that GPs properly examine, diagnose and quickly refer patients to appropriate specialist and other services.

International comparisons generally indicate that England has high-quality cancer screening programmes, although there is considerable regional variation in uptake. The key to improving uptake of screening programmes and ensuring that patients present early is to improve public awareness. I am worried about who will be responsible for promoting public awareness of cancer and running cancer awareness campaigns.

In April 2013, local authorities will take over responsibility for public health. The main focus will be on strategic needs assessment for their local population and developing joint strategic health and well-being strategies, but they will also be responsible for commissioning specific public health services, and they will be free to set their own priorities.

[Mr Baron]

The hon. Lady is absolutely right in saying that cancer survival rates have been improving for 30 to 40 years, but we still lag behind the European average, although I accept that we must be careful when comparing statistics. Will she confirm that, although we heard a lot about the Opposition’s concerns about changes to the commissioning structures, we did not hear much about the other key element of the NHS reforms: the importance of focusing on outcomes, particularly in cancer, as a way to drive forward earlier diagnosis? The spotlight should be on the local NHS and areas with poor outcomes, which should introduce initiatives to drive forward earlier diagnosis, including awareness of cancer screening programmes and so on, but we did not hear a lot about that from Opposition Members.

[Liz Kendall]

I thank the hon. Gentleman for his intervention. He was lucky enough not to experience the 16 weeks of the two Public Bill Committees that considered the Health and Social Care Bill, when I regularly raised the key concerns, such as how to improve outcomes for cancer and heart disease and how services, not structures, needed to be reformed to do that. If he has a spare moment and reads the report of those debates, I am sure that he would become aware that I was very concerned about how to improve patients’ lives, their experience and the quality of care, which is always the issue for me. My concern was always about whether the reforms would do that.

I return to the point that I was making about local authorities’ role and the concern that, under the mandated public health services that local authorities will have to commission, public awareness campaigns, including those for cancer, are not included. There is a real worry among public health professionals and those working for and with cancer patients about whether public health awareness campaigns, such as the bowel cancer awareness campaign, which certainly attracted my attention, will continue.

A second issue is how to improve GPs’ skills and their awareness of cancer. Many GPs see cancer patients relatively infrequently, particularly those with rare cancers. Will the Minister explain what national or local action may be taken to ensure that skills and awareness improve?

We want to ensure that, when people are referred by a GP, they have swift access to diagnostic tests. That is about not just good outcomes, but the quality of their experience. Anyone who has had the misfortune of themselves or a family member waiting for cancer diagnostic tests knows that it is a frightening experience and that it should be done as quickly as possible. There were big improvements under the previous Government in speeding up diagnostic tests, but there is evidence that the service is going backwards. Some 78% more patients now wait more than six weeks for diagnostic tests compared with May 2010, and there are even bigger increases in the number waiting for vital tests to diagnose cancer. Some 230% more patients now wait more than six weeks for endoscopic diagnostic tests, and that includes a 242% increase in the number waiting more than six weeks for colonoscopy and a 140% increase in the number waiting more than six weeks for MRI scans. What action could and should be taken to reduce those diagnostic waits, which is vital to improve one-year survival rates?

Turning to the important issue of treatment variation, I want to put on the record the excellent briefing from the King’s Fund, “How to improve cancer survival”, which goes through the issues in detail, with the best clinical evidence and the implications for services on the ground. Treatment factors can be divided into four main groups: surgery, radiotherapy, cancer drugs and the overall co-ordination of care. On surgery, there is a lot of evidence that the outcomes for many types of cancer might be better in centralised, specialist centres, particularly for complex surgery, because their use can lead to better training for surgeons. If they have a higher case load, doctors develop greater expertise and experience. More specialist support is available, such as nursing and intensive care, as well as superior equipment. One concern that we raised when discussing the Health and Social Care Bill and reorganisation was who will lead the strategic configuration that is needed to centralise some services, such as cancer, into specialist centres.

Radiotherapy has a significant although modest overall impact on five-year mortality rates. Obviously, the optimum proportion of patients with cancer who should receive radiotherapy varies by tumour type and stage, but it is thought that overall around 50% of patients with cancer would benefit from radiotherapy. However, in 2005, the radiotherapy access rate in England was 38%. That was one reason why the former Government introduced a new strategy, “Radiotherapy: developing a world class service for England”, in 2007. Can the Minister update me on any progress on that?

I am sure that the Minister will talk about the cancer drugs fund and the Government’s aim of improving access to such drugs. He will know that concern remains that the fund has not removed variations from the system. There have been underspends in some parts of the country, and some regional cancer drug funds approve drugs that others do not. The King’s Fund raises a bigger question in its document. It says that it is more important to improve access to surgery and radiotherapy overall. It is worried that there has been almost too much attention on the cancer drugs fund and not enough on the variations in radiotherapy and surgery.

I am really concerned about older people and the variation in their care. Will the Minister say whether the Government will look into that specifically? Older people are under-treated, and their outcomes for cancer are worse as a result, even when account is taken of the different types of tumour and the presence of other diseases or co-morbidity. Older people are less likely to receive intensive treatment and more likely to be admitted as an emergency.

Crucially, major international studies show that differences in survival rates between the UK and other countries are greater for older people. We are not sure of the reasons for that based on the evidence, but the King’s Fund suggests that there may be three key issues: even later presentation; co-morbidity with older people having two, three or more other long-term chronic conditions, which may lead to cancer then being misdiagnosed or not diagnosed; and age discrimination and the feeling that, because someone is getting older, their health is perhaps not so important. I am pleased that the Minister will implement the ban on age discrimination in public services that the former Labour Government introduced. I am very keen that the Government look more into that issue as part of their work on cancer.

I wish to say something about co-ordination of care, which, as we know, is important for patients and the patient experience. During debates on the Health and Social Care Bill, we asked whether cancer networks would continue in the NHS and, if so, how they would be funded. In May last year, the Secretary of State for Health said that the Government would fund and support cancer networks in 2012 and that, after that, the NHS Commissioning Board would continue to support and strengthen them. Over a year later, however, the future of cancer networks is still unclear.

The NHS Commissioning Board has recently published early proposals for clinical networks, which include the new strategic clinical networks prescribed by the NHS Commissioning Board. The proposals also mention 14 to 15 overarching networks in England that will cover a specific geographical area and review the work of the prescribed strategic clinical networks every six months. I think, however, that people are still quite confused about how that will work, and the Government’s proposals do not refer specifically to the 28 cancer networks. I therefore ask the Minister whether all 28 current cancer networks will become prescribed strategic clinical networks, or will their number be reduced? How will they fit into the umbrella networks?

Funding is crucial. In response to a parliamentary question on 21 May this year, the Minister stated that strategic health authorities will be given £18.5 million to fund cancer networks in 2012-13, just as in the previous two years. Page 6 of the recent document from the Department of Health, “Progress Update on the Design of the NHSCB” states:

“Around £10 million of the costs of supporting Networks and Senates are expected to count against running costs.”

That seems to imply that the £10 million is to run not only cancer networks but all clinical networks and senates and that would be a cut of £8.5 million to the cancer networks. Will the Minister say whether the £10 million referred to in the document about the future functioning of the NHS Commissioning Board covers all networks, or cancer networks alone? That is a real concern for people who work in cancer networks and are already worried about the future.

I will conclude by mentioning the patient experience. Several hon. Members have rightly mentioned the need for the patient’s experience of a service to be placed at the heart of what the NHS is trying to achieve. I agree with the call from Macmillan Cancer Support and Breakthrough Breast Cancer for the NHS cancer patient experience survey to be included as part of the fourth domain of the NHS outcomes framework, which is about ensuring that people have a positive experience of care.

The cancer patient experience survey shows that the NHS does well on issues such as waiting times, pain control and patients who feel that they have been treated with dignity and respect. It does not, however, do as well as it could on issues such as patients receiving written information about their condition, financial help, clinicians who work well in a hospital and the community and whether there is enough nurse support. Those are important matters for patients.

Oral Answers to Questions

John Baron Excerpts

Tuesday 12th June 2012 Commons Chamber

[Paul Burstow]

I am afraid that I did not entirely hear the hon. Gentleman’s question, but it was about research, and the Government are certainly committed to substantial investment, working with partners to ensure that we have among the best research in the world so that we have access to treatments at the earliest opportunity.

[Mr John Baron (Basildon and Billericay) (Con)]

Does the Minister agree with the recent report by the all-party group on cancer, which found that, if we are to drive improvements and outcomes consistently throughout the NHS, both the one-year and five-year cancer survival rates should be included in the NHS outcomes framework and in the commissioning outcomes framework?

[Paul Burstow]

My hon. Friend, who chairs that all-party group, met me recently to make those points, and as a consequence of that meeting and his excellent note of it I undertook to write to him in greater detail. He will understand that some of those issues go to the heart of data collection and to the quality of the data currently available throughout all cancer sites, and that is the reason why we may not be able to do quite what he wants at the pace that he wants.

Health and Social Care Bill

John Baron Excerpts

Tuesday 28th February 2012 Commons Chamber

[Mr Lansley]

I believe that I answered that question. The point of the letter was to reflect the discussions that we have been having.

[Mr John Baron (Basildon and Billericay) (Con)]

Does my right hon. Friend accept that the debate so far risks ignoring the importance of the Bill’s renewed outcomes? In cancer, for example, such focus is instrumental in driving forward earlier diagnosis, which in itself could save quite literally thousands of lives.

[Mr Lansley]

My hon. Friend is absolutely right, and I am sure that in that context he shares with me the appreciation of the benefit that will come from campaigns to promote the early awareness of cancer, such as, following piloting, the roll-out of the national campaign for the awareness of bowel cancer symptoms.

Oral Answers to Questions

John Baron Excerpts

Tuesday 21st February 2012 Commons Chamber

[Paul Burstow]

I say two things to the hon. Gentleman: first, that the reforms will actually release resources from back-office costs and put them back into the front line, which I hope all hon. Members want to happen; and, secondly, that when it comes to our cancer strategy, we committed additional resources in the spending review to invest in cancer services. If he wants to raise specific issues with me, I will be only too happy to address them.

[Mr John Baron (Basildon and Billericay) (Con)]

The Minister will fully understand the importance of early diagnosis in cancer outcomes and tackling cancer inequalities. May I therefore urge the Government to include the one-year outcome measure in the commissioning outcome framework, so that we can measure the performance of clinical commissioning groups?

[Paul Burstow]

My hon. Friend, who chairs the all-party group on cancer, has been pursuing that issue vigorously. We certainly need to ensure that we use both proxy and other performance indicators on cancer outcomes, and I will want to continue examining whether that indicator is the most appropriate one to tell us what we need to know about improvements in cancer outcomes performance.

Oral Answers to Questions

John Baron Excerpts

Tuesday 12th July 2011 Commons Chamber

[Paul Burstow]

I am surprised that the hon. Lady does not know. As I understand it, there is a date in all three people’s diaries, but it is not for me to share that date. Although we do need to have cross-party talks between the leaders and the health spokespeople involved, we should also look back and draw some lessons from the royal commission on long-term care. What surprises me is that when that report was published by the right hon. Member for Holborn and St Pancras (Frank Dobson), all that was offered was a debate—not a debate that the Government would lead, but a debate that would take place across the country. We are still waiting for the end of that debate. This Government have a timetable and a commitment to engage.

[Mr John Baron (Basildon and Billericay) (Con)]

3. What arrangements he plans to put in place to ensure clinical commissioning groups are held accountable for their performance in respect of cancer outcomes.

[The Secretary of State for Health (Mr Andrew Lansley)]

The first NHS outcomes framework includes a number of outcomes relevant to people with cancer. For example, domain 1, on preventing people from dying prematurely, includes progress in improving one-year and five-year survival rates for breast, lung and colorectal cancers. A number of indicators will also be relevant to patients with cancer, such as health-related quality of life for people with long-term conditions, and improving the experience of care for people at the end of their lives. Clinical commissioning groups will be held to account for their contributions to improving those national outcomes through the commissioning outcomes framework.

[Mr Baron]

The all-party group on cancer and others lobbied for a greater focus on outcomes, but the one-year and five-year cancer survival rates may now be less statistically robust, as CCGs cover smaller population sizes than primary care trusts. Will the Government therefore give added priority to the excellent work of the National Cancer Intelligence Network in producing a set of evidence-based process measures to complement, not replace, other evidence so that CCGs can be held accountable?

[Mr Lansley]

The House will know of my hon. Friend’s consistent support, through the all-party group, for patients with cancer. I entirely agree that a number of proxy measures and process measures will be relevant in the context of the commissioning outcomes framework. There may be measures that are attributable to CCGs individually in some respects. For example, the quality of life of people living with long-term conditions, to which I referred, would be relevant to a small population. For other measures, however, it may be appropriate for the CCGs to be held to account at the level of, for example, a cancer network, using cancer registry data.

NHS Future Forum

John Baron Excerpts

Tuesday 14th June 2011 Commons Chamber

[Mr Lansley]

I reiterate that the clinical commissioning groups will be statutory bodies with a statutory responsibility for commissioning, so it would not be legal for them to delegate that to another body that was not subject to the same obligations. As far as access to private patients is concerned, we have made it clear—I do not believe that the Future Forum makes any recommendations on this—that foundation trusts, which often have arbitrary rules relating to limits on their income from private patients, should have that cap lifted, but we propose to put additional safeguards in place to make it clear that, if they do so, not only must that income be separately accounted for so that there is no subsidisation from NHS facilities, but the trusts must demonstrate how that will support their continuing primary purpose of providing services to the NHS in England.

[Mr John Baron (Basildon and Billericay) (Con)]

Having very much supported the listening exercise, I know that for many of us the most important aspect of these reforms has always been the new focus on outcomes, as illustrated by the inclusion of the one and five-year cancer survival rates in the outcomes framework. Will the Secretary of State assure me that the Future Forum’s suggestions will in no way detract from that new focus on the quality of care?

[Mr Lansley]

I can give my hon. Friend that assurance. Indeed, I can go further and say that one of the reasons the Future Forum has made no recommendations on the outcomes framework is that it found enthusiasm across the NHS for focusing on quality and outcomes and nothing but approval for the framework. Of course, the Labour party ignores the fact that, as stated in the White Paper we published last year, that is one of the central aspects of what we are setting out to do. He is right that the focus on outcomes, which enables people to see how this country performs in health, relative to other countries, and continuous improvement in health outcomes, rather than just a small number of focused targets, is instrumental in continuous improvement.

Oral Answers to Questions

John Baron Excerpts

Tuesday 7th June 2011 Commons Chamber

[Mr Lansley]

My right hon. Friend the Prime Minister has made it very clear that we will not let waiting times rise and that we will improve performance in the NHS right across the board, which was what I was illustrating. I remind the right hon. Gentleman again that waiting times in hospitals are down from 8.4 weeks to 7.9 weeks for in-patients and from 4.3 weeks to 3.7 weeks for out-patients. That is what we are committed to. Chris Ham of the Kings Fund was on the “Today” programme this morning and said on waiting times, “There hasn’t been a great deal of change since the election.” What has changed since the election is that we are improving performance, driving down the number of breaches of the single-sex rules, increasing access to dentistry, cutting the number of managers and increasing the number of doctors. Those are the things we are doing in the NHS, and it is to the benefit of patients that we do.

[Mr John Baron (Basildon and Billericay) (Con)]

3. What steps he is taking to enable GP consortia to commission integrated cancer services.

[The Minister of State, Department of Health (Paul Burstow)]

“Improving Outcomes: A Strategy for Cancer” set out our plans to support GP consortia to commission high-quality cancer services that deliver improved outcomes. The strategy confirmed the importance of cancer networks and we have recently confirmed that the NHS commissioning board will continue to support strengthened cancer networks.

[Mr Baron]

I thank the Minister and the Secretary of State for extending the guaranteed funding for cancer networks to 2013 and their commitment to support them thereafter, because the cancer networks’ expertise will be much valued by consortia. How will the authorisation process for GP consortia ensure effective commissioning of those cancer services that span consortia boundaries, such as radiotherapy?

[Paul Burstow]

What we are doing at the moment with the pause is making sure that we revise the proposals in ways that ensure that we deliver the outcomes set out in the White Paper last year. One of the things we said in the White Paper, and which the Bill currently provides for, is that GP commissioning consortia can collaborate where they need to commission for larger populations.

Future of the NHS

John Baron Excerpts

Monday 9th May 2011 Commons Chamber

[John Healey]

My right hon. Friend is absolutely right, and he draws on his experience as a former Health Minister. While implementation continues apace, there is a so-called pause in the legislation. His point is exactly the one made by the all-party, Tory-led Health Committee in a recent report. If the Prime Minister wants to prove to NHS patients and staff that his pause is not just spin, he must shelve the Bill and make radical changes to his NHS reorganisation plans.

[Mr John Baron (Basildon and Billericay) (Con)]

The shadow Secretary of State speaks as if no reform is needed. However, given that our cancer survival rates are well below the European average and that that costs thousands of lives in this country, does he accept that reform of how the NHS treats cancer patients is necessary?

[John Healey]

The hon. Gentleman has great expertise in, and commitment to, cancer care. He is right that our survival rates continue to lag behind those of parts of Europe, but I am sure he is aware that the rate of fall in deaths from cancer has accelerated in the past decade. On that basis, and with continued investment and reform, we have a chance of catching up to European levels. However, the reforms proposed in the Bill, as many cancer charities and those who represent patients testify, raise the concern that the great gains made by the cancer networks in integrating and co-ordinating services for cancer patients and sufferers will be put at risk.

--- Later in debate ---

[Mr Lansley]

I do not want to correct the hon. Lady, but everything I have been saying up until now has been about defending the NHS and defending our focus on delivering better results by giving the NHS greater front-line devolved responsibility. That is not a matter of debate and disagreement between the coalition parties; we are all in favour of that. The point is this: how can the Bill best support the principles on which we are agreed? I thought the right hon. Member for Wentworth and Dearne and the Labour party were agreed on those principles; that seemed to come out from his interview last week. Indeed, at the end of his speech today I was not quite sure whether or not he agreed with us.

[Mr Baron]

Given that our cancer outcomes are well below the European average, the need for NHS reform is well established. However, as my right hon. Friend the Secretary of State will know from my having raised the issue with him previously, the entire cancer community will breathe a sigh of relief if the guaranteed funding for cancer networks can be extended to 2014 when the transition period for GP commissioning comes to an end, as we would risk losing a lot of expertise if we were to end it in 2012. Will he address that point?

[Mr Lansley]

The support for cancer networks will continue during the course of this year and the start of next year, but when the NHS commissioning board takes responsibility for commissioning, including the relationship with consortia, it will need to decide how to manage its commissioning responsibilities. However, as I have told my hon. Friend in the House previously, it is now looking—we will look at this over the coming months—at how it can use networks as a basis for having precisely the kind of commissioning structures we want, and it is my expectation that that would include cancer networks that are not only helpful for providers, but that tie together commissioners and providers in understanding the future strategy for cancer.