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Three papers published in Thorax address the issue of the late diagnosis of lung cancer. The most recent international population-based survival data for lung cancer again show the UK at the bottom of the scale with a predicted 8.8% of those diagnosed between 2005 and 2007 being alive at 5 years compared with 14.4% in Norway, 16.3% in Sweden and 15–20% in areas of Australia and Canada.1 It has been estimated that, in England, around 1300 lives per year would be saved if our survival matched the best in Europe.2 It is well known that late diagnosis is the major reason why lung cancer outcomes are generally so poor and this is illustrated by the fact that, in the UK, more than 70% of patients have advanced stage (IIIB or IV) disease at the time of diagnosis.3 Huge attention has therefore been focused on the possibility of screening asymptomatic individuals and the most recent findings of the National Lung Cancer Screening Trial4 would appear promising.
In considering reasons underlying the consistent finding of poor UK survival rates, most attention has been given to shortcomings in treatment in secondary care and there is no doubt that there are wide variations in treatment and survival within the UK itself.3 What is not yet known is the extent to which later stage at diagnosis in the UK may explain these survival differences. Some have proposed that at least part of the explanation may be a higher rate of comorbidities in the UK,5 although the evidence for this is limited. One recent study, however, suggests that late diagnosis in the UK is a major factor. Holmberg et al6 compared excess lung cancer deaths at 5 years in different age groups in Sweden, Norway and England. There were considerably more excess deaths in all age groups in England but when patients who died within the first year were excluded the death rates among the countries were similar; indeed most of the excess deaths in England could be explained by deaths in the first 3 months after diagnosis. Since there are no screening programmes in any of these countries, the assumption has to be that symptomatic patients are, for whatever reason, getting treatment earlier in Norway and Sweden than in England. That very late diagnosis is an important issue is well illustrated in work by the National Cancer Intelligence Network. This work showed that in 2007, 38% of all patients with lung cancer in England first presented to secondary care as emergencies. Only 8.9% of these patients were alive at 1 year compared with 39.8% of those referred by an elective route from primary care.7 Several studies have described delays of many weeks or months in patients seeking medical advice for the symptoms of lung cancer.8 9
Simon et al10 developed a robust lung cancer awareness measure and have clearly demonstrated that awareness of the symptoms of, and risk factors for, lung cancer is very poor in the UK, with 38% of the large study sample unable to recall a single symptom. This cancer awareness measure is now being used as a tool in UK-based public awareness campaigns and in an International Cancer Benchmarking Study to examine international differences in public awareness of symptoms. Athey et al11 report the impact of a campaign in Doncaster to raise public and primary care awareness of lung cancer. The message of the campaign was that a persistent cough should trigger people to seek advice from their GP and to ask for a chest x-ray. This innovative project, which is a collaboration of public health, secondary and primary care clinicians, used social marketing techniques to identify and target communities at high risk of developing lung cancer. One particularly effective method adopted by the campaign was to install chips in bus stops so that the sound of coughing was triggered as people approached. This led to wide local press coverage. Although this has to be considered a pilot project, it clearly showed that the campaign resulted in enhanced public recall of cough as an important symptom; a change in behaviour of the public, with more patients going to their GP; a change in behaviour of GPs, with a 20% increase in chest x-ray requests; and an increase in new lung cancer diagnoses, with a suggestion that there were more patients diagnosed with early stage disease. Clearly further work is needed on a larger scale to confirm these findings and to prove that such an approach can have an impact on radical treatment rates and survival. As part of the government's National Awareness and Early Diagnosis Initiative (NAEDI), a joint project between the English Department of Health and Cancer Research UK,12 these findings, taken together with other evidence of late diagnosis referred to above, have led to a number of local public and primary care lung cancer awareness projects and a major public awareness campaign in the Midlands in autumn 2011. This campaign, part of a wider ‘Be Clear on Cancer’ programme, aims to raise awareness of the symptom of a cough lasting for more than 3 weeks and uses TV, radio, press, etc to convey this message. We await the evaluation of these projects with interest.
Coming back to the screening of asymptomatic people, most international efforts aimed at improving early diagnosis of lung cancer have been driven by the often unspoken belief that, by the time patients with lung cancer develop symptoms, the die is cast and the likely long term survival benefits will be small. All of the major recent work on screening has used low-dose CT scanning. Widely divergent, indeed polarised, views have been expressed by a variety of authors on the relative benefits and cost effectiveness of this approach.13 14 One issue which is much less discussed, but that may limit the effectiveness of any screening programme, is whether people at high risk would wish to take part in such programmes.15 This is the subject of the study by Patel et al16 in the context of the Lung-SEARCH trial. The risks of smoking are so well known that the residual smokers (around 21% of adults in the UK17) are probably people with a pattern of high-risk behaviour with a mind set of fatalism and denial who intuitively one would expect to be a group less likely to take up the offer of screening. There is also a strong culture of nihilism around the diagnosis of lung cancer, which is popularly thought of as a universal death penalty. One previous study has added weight to the idea that poor uptake in this group may be an issue, demonstrating that smokers are less likely to participate in lung cancer screening programmes than ex-smokers.18 Patel et al16 reported on the acceptance of annual CT scans, sputum cytometry and bronchoscopy surveillance in smokers and ex-smokers with mild to moderate chronic obstructive pulmonary disease (COPD) who had already consented to take part in the Lung-SEARCH trial. Although the majority of participants found the interventions acceptable, there was evidence of doubt about the value of early detection, particularly in older patients. They also found evidence to support the hypothesis that worry is a factor that deters people from participating in screening. Such considerations clearly need to be built in to cost-effectiveness analyses of any national screening programme.
While it is vital we continue to push for effective screening programmes, those that use current technology are likely to be of limited benefit, costly and not likely to be implemented in the near future, at least in the UK. Strenuous efforts are also needed to find better screening methods that can eventually supersede CT scanning. We simply cannot wait and have to trial—and carefully evaluate—a variety of approaches to promote earlier diagnosis in patients who already have symptoms of lung cancer.
Competing interests MDP is a co-author on the paper by Simon et al, though his contribution was limited to advice on some elements of the text and the conclusions rather than the design or analysis of the study. He is also a participant in the LungSEARCH trial which is the subject of the paper by Patel et al, though he is not a co-author and has not been directly involved in this sub-study or the preparation of the paper. He is the secondary care lead for the NAEDI programme.
Provenance and peer review Commissioned; internally peer reviewed.