Around 50,200 people a year are diagnosed with lung cancer in the UK and around 32,800 die of it: the third most common cancer and the most common cause of cancer death. It is also the cancer where the gap between rich and poor is widest, by a distance. Mortality rates are 102 percent higher for women and 93 percent higher for men in the most deprived fifth of the UK than in the least, around 13,400 lung cancer deaths a year are linked with deprivation, and in Scotland the incidence rate in the most deprived fifth is more than three times the rate in the least. The National Cancer Plan says lung cancer alone accounts for almost a year of the nine-year life expectancy gap between richer and poorer parts of England. Against that, this is also the cancer where the NHS has changed most: England is building a national screening programme, the proportion of English cases found at stage 1 or 2 rose from 32 percent in 2022 to 40 percent in 2024, and the number of people given treatment with curative intent rose from 5,561 to 8,936 between 2019 and 2024. This page follows the NHS route from the lung health check invitation through the chest X-ray rules, the 49-day optimal pathway and the 28, 31 and 62 day standards, to the lung multidisciplinary team, the thoracic surgery units, reflex molecular testing and the drugs. It lists every NICE, Scottish Medicines Consortium and Welsh decision on a lung cancer medicine with its reference and date, and says plainly where a figure could not be found.
How the cancer usually comes to light, then the national standards that time each step. The standards are England's unless the four-nations section says otherwise.
The planned route, and the one that is changing the disease. If your GP record shows you have ever smoked and you are between 55 and 74, you are invited to a lung health check: a telephone, online or face-to-face risk assessment, and if your risk is high enough a low-dose CT scan, usually in a mobile unit in a car park rather than a hospital. Of the people staged through screening in England, 76.2 percent had stage 1 or 2 disease, against 40.2 percent of everyone diagnosed; the range between cancer alliances was 63 to 81 percent. Around 70 percent of screening is delivered in mobile units, deliberately placed where people are four times more likely to smoke. Coverage was about 40 percent of the country at the time of the 2026 audit.
Sources: NHS: lung cancer (page last reviewed 20 August 2026) (2026-08-20); NHS: lung cancer screening (the lung health check: who is invited, the telephone or online risk assessment, the scan in a mobile unit, the result letter within four weeks, and the cancer alliance areas where checks are live; page last reviewed 27 March 2023) (2023-03-27); GOV.UK: new lung cancer screening roll out to detect cancer sooner (Department of Health and Social Care, 26 June 2023): ages 55 to 74 with a GP record of smoking, 270 million pounds a year once fully implemented, up to 9,000 cancers a year and almost a million scans, 76 percent of cancers found at an earlier stage in the first phase, around 70 percent of screening delivered in mobile units in areas where people are four times more likely to smoke (2023-06-26); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04)
The commonest symptomatic route. NICE NG12 recommendation 1.1.2 tells GPs to offer an urgent direct-access chest X-ray to anyone aged 40 or over with two or more of cough, fatigue, shortness of breath, chest pain, weight loss or appetite loss, or with only one of those if they have ever smoked. Recommendation 1.1.3 adds a persistent or recurrent chest infection, finger clubbing, supraclavicular or persistent cervical lymphadenopathy, chest signs consistent with lung cancer, or a raised platelet count. Recommendation 1.1.1 says refer on a suspected cancer pathway straight away for chest X-ray findings that suggest lung cancer, or for unexplained coughing of blood at 40 or over. The National Optimal Lung Cancer Pathway asks for the X-ray to be reported before the patient leaves the department or within 24 hours, and a CT within 72 hours if it is suspicious. It also allows a direct-to-CT route, without an X-ray first, for people at high risk.
Sources: NICE NG12: suspected cancer, recommendations by site (lung and pleural cancers 1.1.1 to 1.1.6), published 23 June 2015, last updated 15 April 2026 (2026-04-15); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01)
Nearly one in three lung cancers in England still comes to light through an emergency admission. The share has fallen slowly, from 33 percent in 2022 to 31.9 percent in 2023 and 30.2 percent in 2024, and the audit notes bluntly that the screening programme's effect has not yet translated into fewer emergency presentations. Wales is lower at 26.4 percent; Northern Ireland is much higher, and its registry compared itself directly with England: 40.5 percent against 33.7 percent for 2018 to 2020. Northern Ireland's routes analysis also shows what the route costs: one-year net survival was 22.9 percent after an emergency presentation against 61.6 percent for people who came through an ordinary outpatient appointment, and 56.8 percent of stage IV cases came this way against 20.8 percent of stage I cases.
Sources: National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); Northern Ireland Cancer Registry 2026: routes to diagnosis 2018 to 2022 (lung: 41.2 percent of diagnoses through an emergency presentation, 40.5 percent in Northern Ireland against 33.7 percent in England for 2018 to 2020) (2026); Cancer Research UK: lung cancer statistics (key stats, early diagnosis and routes by nation, treatment shares) (2026-09-25)
Macmillan's page says around 15 in 100 people diagnosed with lung cancer in the UK have never smoked; the audit found that 10.0 percent of English patients with smoking status recorded had never smoked, though that field was complete for only 45.7 percent of records. University College London Hospitals is running an observational study of lung cancer in never-smokers whose own summary says more than a quarter of adults diagnosed with lung cancer have never smoked. The British group that runs TRACERx supplied the mechanism: fine particulate air pollution promotes EGFR-driven lung adenocarcinoma, and ultradeep sequencing of histologically normal lung tissue from 295 people found oncogenic EGFR variants in 18 percent of samples. Roy Castle Lung Cancer Foundation campaigns on exactly this under the name Let Go of the Labels, arguing that the words smoker and never-smoker distort what is going on and deny people an earlier diagnosis.
Sources: Macmillan Cancer Support: lung cancer (support line 0808 808 00 00, 8am to 8pm every day) (2026-09-25); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); NIHR Be Part of Research: observational study of lung cancer in never-smokers (University College London Hospitals, recruiting; the record carries only a portfolio number, no registry identifier) (2026-07-23); Hill W and others, lung adenocarcinoma promotion by air pollutants, Nature 2023 (particulate matter and EGFR-driven lung cancer across 32,957 cases; oncogenic EGFR variants found in 18 percent of histologically normal lung samples) (2023); Roy Castle Lung Cancer Foundation: campaigns (Let Go of the Labels, This is Lung Cancer, and the policy ask that no one should wait longer than 14 days for genomic testing) (2026-09-25)
The UK National Screening Committee recommended targeted screening in June 2022 for people aged 55 to 74 at high risk, with integrated smoking cessation, and the government approved the recommendation on 26 June 2023. The operating document is NHS England's standard protocol, version 3 of 3 February 2025. Eligibility is age 55 to 74 years and 364 days, registered with a GP practice in England, and having ever smoked, with no baseline scan more than three months after a 75th birthday; because GP smoking records are poor, the protocol says that once the programme is fully rolled out everyone in the age band should be given the opportunity irrespective of their recorded smoking history. GP records are re-queried at least every two years. Who gets a scan is decided by risk models, not by age and pack-years alone. The programme uses PLCOm2012, adapted for UK ethnic groups, at a six-year risk of 1.51 percent or more, and the Liverpool Lung Project model version 2 at a five-year risk of 2.5 percent or more; satisfying either is enough. The Yorkshire Lung Screening Trial is why: at those thresholds PLCOm2012 identified 91.1 percent of the cancers against 62.8 percent for the 2013 United States categorical rule. People are excluded if they are beyond the scanner's weight or size limits, cannot lie flat, are too unwell for treatment with curative intent, are on a palliative care register or are severely frail. The scan is usually in a mobile unit in a car park, should happen within 56 days of the lung health check, and the result letter should arrive within 28 days. A clear scan means a return in 24 months from the last stable or negative scan; an indeterminate nodule means surveillance at three and twelve months first, so a person can be 36 months from their baseline before their next routine round. Nodules are managed on the British Thoracic Society ladder with volumetry preferred, characterised at 5 mm or 80 cubic millimetres, and referred at 300 cubic millimetres or 8 mm with a Brock risk of 10 percent or more. The programme is expected to cost 270 million pounds a year once fully implemented; its modelling assumes 63 percent uptake and that 43.3 percent of completed risk assessments lead to a scan.
Sources: UK National Screening Committee: lung cancer recommendation (June 2022 review): targeted screening with low-dose computed tomography is recommended for people aged 55 to 74 at high risk, with integrated smoking cessation, and the Targeted Lung Health Checks programme is a feasible starting point in England (2022-06); NHS England: targeted screening for lung cancer with low radiation dose computed tomography, the standard protocol prepared for the Lung Cancer Screening Programme, publication reference PR1646, version 3 of 3 February 2025 (eligibility, the two risk models and their thresholds, the invitation route, the exclusions, the scan interval and the nodule ladder). The publication page itself answers HTTP 202 with an empty body (2025-02-03); NHS England: quality assurance standards prepared for the Lung Cancer Screening Programme, publication reference PR1647, version 3 of 3 February 2025 (the scan within 56 days of the lung health check, and outcome letters within 28 days) (2025-02-03); Department of Health and Social Care: equality impact assessment for screening for lung cancer (published 24 July 2025), which records that the government approved the UK National Screening Committee's recommendation on 26 June 2023 and that people with no nodules are reinvited every two years (2025-07-24); NHS: lung cancer screening (the lung health check: who is invited, the telephone or online risk assessment, the scan in a mobile unit, the result letter within four weeks, and the cancer alliance areas where checks are live; page last reviewed 27 March 2023) (2023-03-27); GOV.UK: new lung cancer screening roll out to detect cancer sooner (Department of Health and Social Care, 26 June 2023): ages 55 to 74 with a GP record of smoking, 270 million pounds a year once fully implemented, up to 9,000 cancers a year and almost a million scans, 76 percent of cancers found at an earlier stage in the first phase, around 70 percent of screening delivered in mobile units in areas where people are four times more likely to smoke (2023-06-26); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); Department of Health and Social Care: National Cancer Plan technical annex (published 4 February 2026), which gives the programme's operating assumptions: a 63 percent uptake rate, 43.3 percent conversion from risk assessment to scan, a 0.9 percent cancer rate at the first scan and 0.6 percent at later rounds, and a 76 percent early diagnosis rate against 29 percent before the programme (2026-02-04); Gabe R and others, comparing eligibility criteria in the Yorkshire Lung Screening Trial, Journal of Thoracic Oncology 2025 (the PLCOm2012 risk model at 1.51 percent found 91.1 percent of cancers against 62.8 percent for the 2013 US Preventive Services Task Force rule) (2025)
NG12's lung rules are unchanged since 2015 and are unusually permissive: two unexplained symptoms at 40 or over, or one if you have ever smoked. The National Optimal Lung Cancer Pathway then tries to compress what follows: the X-ray reported before the patient leaves or within 24 hours, CT the same day or within 72 hours, triage by radiology or respiratory medicine by day 3. Version 4 of the pathway, published 1 January 2024, added a direct-to-CT route for people at high risk of symptomatic lung cancer, clarified the other urgent presentation routes, and added blood-based tumour diagnostics and a molecular testing pathway. The National Cancer Plan says the artificial intelligence diagnostic fund has already put chest X-ray analysis tools into almost half of trusts and will extend them to all, and that self-referral for chest X-ray will be expanded; Roy Castle hosts the standard operating procedures of the three established self-request programmes, in Leeds, Greater Manchester and Leicester.
Sources: NICE NG12: suspected cancer, recommendations by site (lung and pleural cancers 1.1.1 to 1.1.6), published 23 June 2015, last updated 15 April 2026 (2026-04-15); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); Roy Castle Lung Cancer Foundation: self-request chest X-ray services, a resource hub carrying the standard operating procedures of the Leeds, Greater Manchester and Leicester programmes (2026-09-25); NICE HTG696: artificial-intelligence-derived software to analyse chest X-rays for suspected lung cancer in primary care referrals, early value assessment (28 September 2023, last updated 10 February 2025) (2025-02-10)
England measures the time from an urgent suspected cancer referral, an urgent screening referral or a consultant upgrade to the day the patient is told. In July 2026 the NHS achieved 79.3 percent across all cancers; for suspected lung cancer it was 77.8 percent, made up of 82.2 percent on the urgent suspected cancer route and only 58.9 percent on the national screening programme route. The National Cancer Plan commits to 80 percent by March 2029. For lung cancer the constraint is diagnostic capacity: GIRFT's lung cancer report asked for a three working day turnaround from abnormal chest X-ray to CT report, key diagnostic investigations within 21 calendar days, PET-CT reported within five calendar days, image-guided biopsy within five working days and endobronchial ultrasound within five calendar days, and found that in the 2019 organisational audit only 46 percent of services met the three-day target. NHS England's cancer waiting times web pages answer HTTP 202 with an empty challenge to automated readers; the figures here were read from the statistical release and the monthly data file, which do resolve.
Sources: GOV.UK: waiting times for suspected and diagnosed cancer patients, July 2026 (the definitions of the 28, 31 and 62 day standards; published 10 September 2026) (2026-09-10); NHS England: cancer waiting times statistical release for July 2026, provider based, provisional (released 10 September 2026): 79.3 percent on the 28-day standard, 92.5 percent on the 31-day and 71.2 percent on the 62-day (2026-09-10); NHS England: cancer waiting times monthly combined data, April to July 2026, provisional (the lung rows for July 2026: 77.8 percent on the 28-day standard and 60.9 percent on the 62-day, and 35.9 percent at 62 days for referrals from the screening programme) (2026-09-10); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); GIRFT: lung cancer, national specialty report (Paul Beckett, Sarah Doffman and Elizabeth Toy, October 2021): 33 recommendations, including an 85 percent radical treatment rate in stage I to II, a surgical resection rate above 20 percent and a ten calendar day turnaround for molecular profiling (2021-10); NHS England: cancer waiting times statistics (the page answered HTTP 202 with an empty AWS web application firewall challenge to OnCo on 25 September 2026)
NICE NG122 recommendation 1.2.2 asks for contrast-enhanced CT including the liver, adrenals and lower neck, and 1.2.14 says do it before any biopsy. Recommendation 1.2.4 says ensure everyone who could potentially have treatment with curative intent is offered PET-CT before treatment, and 1.2.5 asks every cancer alliance to have a system of rapid access to it. Recommendation 1.2.8 offers endobronchial ultrasound-guided transbronchial needle aspiration for paratracheal and peribronchial lesions, and 1.2.9 asks every cancer alliance to have at least one centre with endobronchial or endoscopic ultrasound. Recommendations 1.2.31 to 1.2.33 require every suspected case to be referred to a member of a lung cancer multidisciplinary team, every working diagnosis to be discussed at that team's meeting, and fast-track lung cancer clinics to exist. The optimal pathway asks that a surgeon be present at more than 95 percent of meetings and that the full team meeting happen by day 21. NHS England's timed lung cancer diagnostic pathway names the core membership, which NG122 itself does not: lead clinician, radiologist, pathologist, oncologist, clinical nurse specialist and a relevant allied health professional, working with a pathway navigator, with a named clinical lead for every team. Its day-by-day audit tool runs from the chest X-ray at day minus three to triage at day 3, the fast-track clinic at day 6, a test bundle including at least PET-CT and spirometry at day 14, the multidisciplinary team meeting at day 21 and follow-up at day 28. Staging in NG122 still uses the seventh edition of the American Joint Committee on Cancer system; brain imaging is not offered in clinical stage 1 disease without neurological symptoms, is CT in stage 2 and MRI in stage 3.
Sources: NICE NG122: diagnosis and staging (the CT, PET-CT, EBUS-TBNA and sampling recommendations 1.2.1 to 1.2.34, including the multidisciplinary team and the lung cancer clinical nurse specialist) (2026-02); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); NHS England: implementing a timed lung cancer diagnostic pathway, publication reference PRN1346 (12 October 2023, last modified 25 June 2024), by Peter Johnson and David Baldwin: the day-by-day audit tool and the core membership of the lung cancer multidisciplinary team (2024-06-25); GIRFT: lung cancer, national specialty report (Paul Beckett, Sarah Doffman and Elizabeth Toy, October 2021): 33 recommendations, including an 85 percent radical treatment rate in stage I to II, a surgical resection rate above 20 percent and a ten calendar day turnaround for molecular profiling (2021-10)
NG122 recommendation 1.2.11 says samples must be adequate to allow tumour subtyping and the assessment of molecular markers, and 1.2.12, amended in February 2026, now points directly at the National Genomic Test Directory for the next-generation sequencing panels, having previously described single-mutation testing. The National Optimal Lung Cancer Pathway sets the clock: tissue acquired on day 0, morphology and slide preparation for reflex testing by day 3, PD-L1 immunohistochemistry and slide preparation locally, then reflex sequencing, with a full molecular report no more than 14 calendar days after the sample was taken and the treating specialist seeing the patient within three working days of the result. Both DNA and RNA sequencing should be done in any histological subtype of non-small-cell disease. If there is not enough tissue, the pathologist emails or telephones the lung multidisciplinary team the same day, and the team decides between repeat sampling (allowed to day 21) and a salvage route: a limited DNA panel, fluorescence in situ hybridisation for ALK and ROS1, and a blood predictive biomarker. Circulating tumour DNA testing for non-small-cell lung cancer was added to the National Genomic Test Directory in May 2025 after an NHS pilot in which results came back on average 16 days faster than tissue genotyping. GIRFT asked for a maximum ten calendar day turnaround, and Roy Castle campaigns for 14 days as a patient right.
Sources: NICE NG122: diagnosis and staging (the CT, PET-CT, EBUS-TBNA and sampling recommendations 1.2.1 to 1.2.34, including the multidisciplinary team and the lung cancer clinical nurse specialist) (2026-02); NICE NG122: update information (February 2026 amended recommendation 1.2.12 from single-mutation testing to comprehensive next-generation sequencing panels through genomic laboratory hubs, and added links to the technology appraisals; March 2024 removed the mobocertinib pathways after that guidance was withdrawn) (2026-02); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); GIRFT: lung cancer, national specialty report (Paul Beckett, Sarah Doffman and Elizabeth Toy, October 2021): 33 recommendations, including an 85 percent radical treatment rate in stage I to II, a surgical resection rate above 20 percent and a ten calendar day turnaround for molecular profiling (2021-10); Roy Castle Lung Cancer Foundation: campaigns (Let Go of the Labels, This is Lung Cancer, and the policy ask that no one should wait longer than 14 days for genomic testing) (2026-09-25)
NG122 recommendation 1.1.1 says a lung cancer clinical nurse specialist should be available at all stages of care, and 1.2.34 says every cancer unit or centre should have one or more, seeing people before, at and after diagnosis. The audit's problem is not the number but the record: among English patients who had the field filled in, 93.1 percent had contact with a nurse specialist, comfortably above the 90 percent target, but the field was complete for only 64.2 percent of records and no English trust met the completeness target. Only 56 trusts exceeded 70 percent completeness. Wales records it for 97.5 percent of patients and reports 94.9 percent contact. The audit launched a quality improvement initiative on this indicator in autumn 2025.
Sources: NICE NG122 recommendation 1.1.1: a lung cancer clinical nurse specialist should be available at all stages of care (2026-02); NICE NG122: diagnosis and staging (the CT, PET-CT, EBUS-TBNA and sampling recommendations 1.2.1 to 1.2.34, including the multidisciplinary team and the lung cancer clinical nurse specialist) (2026-02); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02)
NG122 recommendations 1.3.1 to 1.3.3 are short and specific: tell people that smoking increases the risk of pulmonary complications after lung cancer surgery, advise them to stop as soon as the diagnosis is suspected and say why, and do not postpone surgery to allow them to stop. The National Cancer Plan commits hospitals to integrating opt-out cessation support into all routine care and to including smoking status in clinical assessments for non-urgent operations, with 70 million pounds more for local authority stop smoking services. Inside screening the evidence is British and good: in the Yorkshire Lung Screening Trial 89 percent of eligible smokers accepted an immediate consultation with a cessation practitioner at the same appointment, 75 percent took ongoing support and 12.4 percent were carbon-monoxide-validated quitters at four weeks. The UK National Screening Committee's recommendation was explicitly for screening with integrated smoking cessation, not screening alone. Outside screening, NICE NG209 section 1.14 asks secondary care to offer behavioural support during the current outpatient visit or inpatient stay, to provide it immediately at the outpatient site including at preoperative assessment, and to send people home with at least a week of stop-smoking medicine. The NHS Long Term Plan commitment that NHS England publishes covers inpatients, maternity and mental health settings rather than outpatient clinics.
Sources: NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); Murray RL and others, a co-located stop-smoking service inside lung screening, European Respiratory Journal 2024 (89 percent of eligible smokers accepted an immediate consultation; 12.4 percent were carbon-monoxide-validated quitters at four weeks) (2024); UK National Screening Committee: lung cancer recommendation (June 2022 review): targeted screening with low-dose computed tomography is recommended for people aged 55 to 74 at high risk, with integrated smoking cessation, and the Targeted Lung Health Checks programme is a feasible starting point in England (2022-06); NICE NG209: tobacco, preventing uptake, promoting quitting and treating dependence (published 30 November 2021, last updated 4 February 2025), section 1.14 on secondary care, which asks for immediate behavioural support at the outpatient site and a week's pharmacotherapy on discharge (2025-02-04); NHS England: tobacco dependency programme (last modified 23 December 2024), which records the NHS Long Term Plan commitment to tobacco dependency treatment for all overnight inpatients by the end of 2023/24 (2024-12-23)
Scotland is the only nation that publishes a lung-specific split, and lung does well on this measure: 1,033 of 1,050 eligible referrals, or 98.4 percent, started treatment within 31 days in the quarter ending 31 March 2026, with a median wait of two days, against an all-cancer figure of 94.5 percent. The audit's equivalent internal measure is harsher: the median time from the decision to treat to the start of systemic anti-cancer therapy was 16 days in England, and in small-cell lung cancer, where the tumour doubles fastest, the audit's own standard is that at least 80 percent should start within 14 days of pathological diagnosis and only 44 percent did. England achieved 92.5 percent across all cancers in July 2026 and 94.3 percent for lung. Northern Ireland, whose target is 98 percent, treated 110 of 125 lung patients within 31 days in January 2026, 89 of 94 in February and 114 of 127 in March, with a median wait of eight to eleven days.
Sources: GOV.UK: waiting times for suspected and diagnosed cancer patients, July 2026 (the definitions of the 28, 31 and 62 day standards; published 10 September 2026) (2026-09-10); NHS England: cancer waiting times statistical release for July 2026, provider based, provisional (released 10 September 2026): 79.3 percent on the 28-day standard, 92.5 percent on the 31-day and 71.2 percent on the 62-day (2026-09-10); NHS England: cancer waiting times monthly combined data, April to July 2026, provisional (the lung rows for July 2026: 77.8 percent on the 28-day standard and 60.9 percent on the 62-day, and 35.9 percent at 62 days for referrals from the screening programme) (2026-09-10); Public Health Scotland: cancer waiting times, table 1, compliance with standard (quarter ending 31 March 2026): lung 83.6 percent at 62 days and 98.4 percent at 31 days (2026-06-30); Northern Ireland Department of Health: cancer waiting times, January to March 2026 (published 2 July 2026, last updated 11 September 2026), whose tumour-site tables give the lung 31-day performance (2026-09-11); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02)
This is where lung cancer care in England fails most clearly, and the audit measures it against the tighter clinical standard rather than the national one. Of people with stage 1 or 2 non-small-cell lung cancer having surgery in England in 2024, the median time from referral to operation was 81 days and only 12 percent were treated within 49 days; for radical radiotherapy the median was 98 days and 3.2 percent met the target; for systemic therapy in stage 3B to 4 disease the median was 63 days and 27 percent met it. The audit's commentary says the growth in demand for surgery is lengthening the wait and that this will continue as screening expands, and it names thoracic surgery capacity as a priority. The national figures say the same thing: in July 2026, 71.2 percent of people across all cancers started treatment within 62 days, but only 60.9 percent of people with lung cancer, and only 35.9 percent of those referred through the screening programme. Lung cancer is about ten points worse than the average, and the screening route, which exists to catch cancer early, is the slowest door in the building. Scotland is the mirror image: it reported 83.6 percent of lung referrals treated within 62 days in the quarter to March 2026, well above its all-cancer figure of 72.2 percent though below its 95 percent standard, ranging from 67.7 percent in Greater Glasgow and Clyde to 94.1 percent in Lanarkshire. Wales publishes only an all-cancer figure, 60.1 percent in July 2026 against a 75 percent target. Northern Ireland republished its 62-day figures on 11 September 2026 after an error in the encompass patient administration system inflated them: the corrected all-cancer performance for the quarter to March 2026 is 29.6 percent.
Sources: NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); NHS England: cancer waiting times monthly combined data, April to July 2026, provisional (the lung rows for July 2026: 77.8 percent on the 28-day standard and 60.9 percent on the 62-day, and 35.9 percent at 62 days for referrals from the screening programme) (2026-09-10); Public Health Scotland: cancer waiting times, table 1, compliance with standard (quarter ending 31 March 2026): lung 83.6 percent at 62 days and 98.4 percent at 31 days (2026-06-30); Welsh Government: NHS activity and performance summary, July and August 2026 (published 17 September 2026): 60.1 percent of suspected cancer pathways started treatment within 62 days against a 75 percent target; no lung-specific figure is published (2026-09-17); Northern Ireland Department of Health: revised cancer waiting times against the 62-day target (published 11 September 2026), after an error in the encompass patient administration system's suspension logic inflated performance: 29.6 percent in the quarter to 31 March 2026 (2026-09-11); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04)
NG122 recommendation 1.5.1 offers lobectomy, open or thoracoscopic, and 1.5.2 reserves more extensive surgery for clear margins; 1.5.3 requires hilar and mediastinal lymph node sampling or en bloc resection in every curative operation. Recommendation 1.5.5 offers stereotactic ablative radiotherapy or sublobar resection to people with stage 1 to 2A disease who decline lobectomy or in whom it is contraindicated. VIOLET, the UK trial, showed keyhole surgery leaves people with better physical function at five weeks and fewer serious adverse events after discharge, with the same survival at a year. In England in 2024, 7,878 people had surgery, 21.8 percent of everyone with non-small-cell disease, up from 6,547 and 19.6 percent in 2023; resection rates ranged from 15 to 37 percent between cancer alliances. Ninety-day survival after resection was 98.4 percent across England and Wales, on 8,559 operations in 28 thoracic units. Fitness still decides: among people with stage 1 or 2 disease, 75.3 percent with performance status 0 had surgery, 52.2 percent with performance status 1 and 19.2 percent with performance status 2.
Sources: NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); National Lung Cancer Audit: State of the Nation 2026, data tables (the 90-day postoperative survival sheet names every NHS thoracic unit in England and Wales with its 2024 resection count) (2026-02); Lim E and others, VIOLET: video-assisted thoracoscopic or open lobectomy in early-stage lung cancer, NEJM Evidence 2022 (503 randomised; better physical function at five weeks and fewer serious adverse events after discharge with keyhole surgery, same survival at a year) (2022); GIRFT: lung cancer, national specialty report (Paul Beckett, Sarah Doffman and Elizabeth Toy, October 2021): 33 recommendations, including an 85 percent radical treatment rate in stage I to II, a surgical resection rate above 20 percent and a ten calendar day turnaround for molecular profiling (2021-10)
NG122 recommendation 1.5.8 offers stereotactic ablative radiotherapy to people with stage 1 to 2A disease who decline surgery or in whom it is contraindicated, and conventional or hyperfractionated radiotherapy if that too is contraindicated; 1.5.11 says follow the SABR Consortium guidance on fractionation; 1.5.12 sets the conventional doses. Recommendation 1.5.7 asks that everyone treated with curative intent be included in a national quality assurance programme. Britain's contribution here is CHART, invented at Mount Vernon, which gave the whole dose in twelve consecutive days and cut the relative risk of death by about a quarter; the schedule proved hard to run and modern practice uses the doses above, but the biological argument it settled, that tumour repopulation during a long course costs lives, is still the reason radiotherapy courses are kept short. In England in 2024 the median wait from referral to radical radiotherapy in stage 1 to 2 disease was 98 days, the longest interval the audit measures.
Sources: NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02); Saunders M and others, continuous hyperfractionated accelerated radiotherapy against conventional radiotherapy in non-small-cell lung cancer, Lancet 1997 (563 patients, 24 percent reduction in the relative risk of death, two-year survival 20 to 29 percent) (1997); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02)
NG122 recommendation 1.6.1 requires assessment by both a thoracic oncologist and a thoracic surgeon; 1.6.3 to 1.6.5 offer chemoradiotherapy with surgery for operable stage 3A N2 disease, with the operation scheduled three to five weeks after the chemoradiotherapy finishes; 1.6.7 says centres performing lung resections should validate their data for the National Lung Cancer Audit. The guideline now also carries the perioperative appraisals directly: neoadjuvant nivolumab with chemotherapy (TA876), perioperative durvalumab (TA1030), perioperative pembrolizumab (TA1017) and perioperative nivolumab (TA1127), plus adjuvant osimertinib (TA1043), alectinib (TA1014), atezolizumab (TA1071) and pembrolizumab (TA1037). For unresectable stage 3 disease, durvalumab after concurrent chemoradiotherapy (TA798) and, for EGFR-mutant disease, osimertinib after chemoradiotherapy (TA1156). The audit's first recommendation for 2026 is about this step: only 59.1 percent of English patients with stage 3A disease and performance status 0 to 2 were given treatment with curative intent, and it asks cancer alliances to audit their multidisciplinary team decisions to find out why.
Sources: NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); NICE TA1127: nivolumab with chemotherapy before surgery then alone after surgery for resectable non-small-cell lung cancer (4 February 2026; recommendation 1.2 says use the least expensive of nivolumab, pembrolizumab and durvalumab) (2026-02-04); NICE TA798: durvalumab for maintenance treatment of unresectable non-small-cell lung cancer after platinum-based chemoradiation (22 June 2022, PD-L1 of 1 percent or more and only after concurrent chemoradiotherapy; the PACIFIC indication) (2022-06-22)
The funding table below sets out what is available by biomarker. The audit's finding is that access, not availability, is the constraint: 63.4 percent of English patients with stage 3B to 4 non-small-cell disease and performance status 0 to 1 received systemic therapy in 2024, essentially unchanged since 2022, against a 70 percent standard that only 42 of 123 trusts met, with cancer alliance rates ranging from 42 to 84 percent. In small-cell disease 71.2 percent received systemic therapy, just over the standard but down from 73.8 percent in 2023. The audit concludes that the growing demand for systemic treatment is outpacing service provision and asks for a review of capacity, naming molecular pathology capacity specifically.
Sources: National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02); NHS England: national Cancer Drugs Fund list version 1.408, updated 24 September 2026, read in full (320 pages): four lung indications in the Cancer Drugs Fund section and 43 routinely funded lung indications in section B, each with its Blueteq form, appraisal reference and funding date (2026-09-24)
Small-cell disease was 6.6 percent of English lung cancers in 2024, down from 8.6 percent in 2019, and 9.1 percent in Wales. NG122 recommendation 1.8.1 asks for assessment by a thoracic oncologist within one week of the decision to recommend treatment. In limited-stage disease, 1.10.1 offers four to six cycles of cisplatin-based chemotherapy, 1.10.2 offers twice-daily radiotherapy concurrent with it starting in cycle one or two, 1.10.5 offers prophylactic cranial irradiation at 25 Gy in ten fractions, and 1.10.6 now carries durvalumab after chemoradiotherapy (TA1099). In extensive-stage disease, 1.11.1 to 1.11.3 offer platinum chemotherapy with durvalumab (TA1041) or atezolizumab (TA638), and 1.11.4 and 1.11.5 consider thoracic radiotherapy and prophylactic cranial irradiation after a response. The twice-daily schedule survives because of CONVERT, a Manchester-led trial funded by Cancer Research UK across 73 centres in eight countries, which was designed to show the once-daily schedule was better and did not. In relapse, oral topotecan is the only recommended drug (TA184) and tarlatamab was refused (TA1091). The audit's fourth recommendation is about speed: the median time from diagnosis to treatment was 16 days against a 14-day standard, and only 44 percent were treated in time.
Sources: NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); Faivre-Finn C and others, CONVERT, Lancet Oncology 2017 (547 patients; median survival 30 months twice-daily against 25 months once-daily, hazard ratio 1.18, so twice-daily 45 Gy remained the standard) (2017); NICE TA1099: durvalumab for limited-stage small-cell lung cancer after platinum-based chemoradiotherapy (1 October 2025, the ADRIATIC indication) (2025-10-01); NICE TA1091: tarlatamab for extensive-stage small-cell lung cancer after two or more treatments, not recommended (20 August 2025) (2025-08-20)
The audit's fifth recommendation for 2026 asks that everyone diagnosed with stage 1 to 3 disease be recommended regular aerobic and resistance exercise during treatment with curative intent, including preoperative exercise before lung cancer surgery, citing the American Society of Clinical Oncology's 2022 guideline. It made this recommendation because the proportion of people with stage 1 to 2 disease having surgery falls so steeply with fitness. The National Optimal Lung Cancer Pathway asks teams to optimise comorbidities, smoking and nutrition as early as possible and to refer to local prehabilitation services, and the National Cancer Plan promises a digital-first prehabilitation offer through the NHS App. Fit 4 Surgery 2, a 902-patient NIHR trial run from Birmingham across 20 thoracic units, is testing whether an app-based programme actually reduces complications.
Sources: National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); ISRCTN40412033: Fit 4 Surgery 2, an app-based prehabilitation programme before and after lung cancer surgery (University of Birmingham, NIHR; target 902, 20 thoracic units) (2026-09-25)
34 centre entries across 4 nations, with what each offers for this cancer. The service model note below says what happens only at a specialist centre and what can be given closer to home under its MDT.
Lung cancer is diagnosed almost everywhere and operated on in very few places. The National Lung Cancer Audit counted 123 English NHS trusts caring for people with lung cancer in 2024, but its data tables name only 28 NHS thoracic units in England and Wales that perform lung cancer resections: 26 in England and 2 in Wales, between them doing 8,559 operations with a 98.4 percent 90-day survival rate. Every English and Welsh unit except one is listed above with the number of resections it did in 2024, read from that workbook; Blackpool Teaching Hospitals, which did 261, has no card because its website did not respond to any request during the check. NHS England's thoracic surgery service specification 170016/S sets the volume rules: every unit should perform at least 150 lung cancer resections a year, a target set for 2018/19, and none should run a lung cancer surgical service with fewer than 70 patients a year; a unit needs at least three full-time thoracic surgeons and a catchment of around 1.5 million people. On the 2024 numbers, 16 of the 28 units were above 250 resections and four were below 170; Swansea Bay, at 64, is below the specification's floor, though the specification applies to England. Scotland and Northern Ireland are not in the audit at all, so no comparable resection counts exist for them. Scotland has three adult cardiothoracic surgery centres, identifiable from Public Health Scotland's activity data for 2024/25: the Golden Jubilee National Hospital in Clydebank (18,846 episodes), the Royal Infirmary of Edinburgh (16,539) and Aberdeen Royal Infirmary (4,900); Glasgow Royal Infirmary, sometimes listed elsewhere, recorded none. Northern Ireland runs a single regional thoracic service across Belfast City Hospital and the Royal Victoria Hospital. In Wales the audit records resections against Cardiff and Vale and Swansea Bay, though only Swansea Bay publishes a cardiothoracic surgery service page. The audit's third recommendation for 2026 is that providers ensure sufficient thoracic surgery capacity for the growth in demand from screening.
Sources: National Lung Cancer Audit: State of the Nation 2026, data tables (the 90-day postoperative survival sheet names every NHS thoracic unit in England and Wales with its 2024 resection count) (2026-02); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); NHS England: thoracic surgery (adults) service specification 170016/S (the volume rules: every unit to perform at least 150 lung cancer resections a year by 2018/19, and none below 70; 29 units in England, minimum three full-time thoracic surgeons and a catchment of around 1.5 million) (2017-07); Public Health Scotland: cancer waiting times, table 1, compliance with standard (quarter ending 31 March 2026): lung 83.6 percent at 62 days and 98.4 percent at 31 days (2026-06-30); Northern Ireland Cancer Registry 2026: routes to diagnosis 2018 to 2022 (lung: 41.2 percent of diagnoses through an emergency presentation, 40.5 percent in Northern Ireland against 33.7 percent in England for 2018 to 2020) (2026)
By line of treatment: England's NICE decision (which binds Wales and is adopted in Northern Ireland) and Scotland's SMC decision, each with its reference and date. Generic medicines were never appraised and are funded through national chemotherapy protocols.
| Line | Treatment | England (NICE) | Scotland (SMC) | Wales and Northern Ireland |
|---|---|---|---|---|
| Stage 1 to 2, fit for surgery | Lobectomy, open or thoracoscopic, with hilar and mediastinal lymph node sampling; sublobar resection or stereotactic ablative radiotherapy if lobectomy is declined or contraindicated 7,878 operations in England in 2024, 21.8 percent of everyone with non-small-cell disease, against an audit standard of 17 percent and a GIRFT recommendation of more than 20 percent. Scotland's three cardiothoracic centres are the Golden Jubilee National Hospital, the Royal Infirmary of Edinburgh and Aberdeen Royal Infirmary. | NHS England Not a drug decision: NICE NG122 recommendations 1.5.1 to 1.5.8 set the standard, and thoracic surgery is commissioned nationally under service specification 170016/S. VIOLET, the UK trial, established that keyhole surgery leaves people functioning better at five weeks with the same survival | Not checked | Wales: NICE NG122 applies. Wales has two thoracic units, at Cardiff and Vale and Swansea Bay, which did 162 and 64 resections in 2024; the Welsh resection rate was 17.1 percent. NI: NICE NG122 applies. Thoracic surgery is a single regional service run by the Belfast Health and Social Care Trust across Belfast City Hospital and the Royal Victoria Hospital; Northern Ireland is not in the national audit, so no resection rate is published. |
| After complete resection (adjuvant), EGFR mutation-positive | Osimertinib for three years | NICE TA10432025-02-26 Recommended for adjuvant treatment of completely resected stage 1B to 3A non-small-cell lung cancer with EGFR exon 19 deletions or the exon 21 L858R substitution; stop at three years, or earlier on recurrence or unacceptable toxicity. Routinely funded from 27 May 2025 (Blueteq OSI3) | SMC SMC23832021-11-08 Accepted for restricted use for adjuvant treatment after complete resection of stage 1B to 3A disease, under the orphan equivalent process with PACE (SMC2383, 8 November 2021), more than three years before NICE | Wales: NICE TA1043 applies; the All Wales Therapeutics and Toxicology Centre's record for osimertinib is marked excluded from AWMSG appraisal because NICE has appraised it. NI: NICE TA1043 applies through the Department of Health. |
| After complete resection (adjuvant), ALK-positive | Alectinib | NICE TA10142024-11-13 Recommended for adjuvant treatment of completely resected stage 1B (tumours of at least 4 cm) to 3A ALK-positive non-small-cell lung cancer, the ALINA indication. Routinely funded from 11 February 2025 (Blueteq ALE2) | SMC SMC27492025-04-07 Accepted for use within NHSScotland for the same indication (SMC2749, 7 April 2025) | Wales: NICE TA1014 applies. Wales's only AWMSG-authored alectinib decision is a 2017 statement of advice refusing endorsement of the post-crizotinib indication after a non-submission, now superseded by NICE. NI: NICE TA1014 applies. |
| After complete resection (adjuvant), no driver mutation | Atezolizumab if PD-L1 is 50 percent or more, or pembrolizumab, after platinum-based chemotherapy TA1037 is the pembrolizumab appraisal referred to here. | NICE TA10712025-06-19 Atezolizumab recommended for adjuvant treatment of resected non-small-cell lung cancer with PD-L1 on 50 percent or more of tumour cells, at high risk of recurrence and without EGFR mutations or ALK rearrangements (the IMpower010 indication); routinely funded from 21 July 2025 (Blueteq ATE10). Pembrolizumab monotherapy recommended for adjuvant treatment after complete resection and platinum chemotherapy in TA1037 (5 February 2025), routinely funded from 6 May 2025 | SMC SMC24922022-08-08 Atezolizumab accepted for adjuvant use after complete resection of stage 2 to 3A disease with PD-L1 of 50 percent or more (SMC2492, 8 August 2022), nearly three years before NICE. Pembrolizumab accepted for restricted use in the adjuvant setting (SMC2689, 7 October 2024) | Wales: Both NICE appraisals apply. NI: Both NICE appraisals apply. |
| Resectable disease, before and after surgery (perioperative) | Nivolumab, durvalumab or pembrolizumab with platinum-based chemotherapy before surgery, then the antibody alone after it The single widest England-Scotland divergence on this page: three perioperative regimens funded in England, Wales and Northern Ireland and none in Scotland. | NICE TA11272026-02-04 Perioperative nivolumab with chemotherapy recommended for resectable tumours of at least 4 cm or node-positive disease without EGFR or ALK alterations (the CheckMate-77T indication); recommendation 1.2 tells teams to use the least expensive of nivolumab, pembrolizumab and durvalumab. Neoadjuvant nivolumab alone is TA876 (22 March 2023), perioperative pembrolizumab TA1017 (20 November 2024) and perioperative durvalumab TA1030 (15 January 2025). All four are routinely funded | SMC SMC28742025-10-13 Scotland funds none of the perioperative regimens. Neoadjuvant nivolumab alone was accepted (SMC2619, 11 December 2023), but perioperative pembrolizumab was not recommended (SMC2688, 11 November 2024), perioperative durvalumab was not recommended (SMC2677, 9 December 2024) and perioperative nivolumab was not recommended in the absence of a submission (SMC2874, 13 October 2025) | Wales: All four NICE appraisals apply, so Wales funds what England funds. NI: All four NICE appraisals apply. |
| Stage 3 unresectable, after chemoradiotherapy | Durvalumab if PD-L1 is 1 percent or more; osimertinib instead if the tumour is EGFR mutation-positive | NICE TA7982022-06-22 Durvalumab recommended as maintenance treatment of unresectable non-small-cell lung cancer with PD-L1 expression on 1 percent or more of tumour cells whose disease has not progressed after concurrent platinum-based chemoradiation, the PACIFIC indication; only after concurrent, not sequential, chemoradiotherapy. Osimertinib recommended for EGFR mutation-positive unresectable stage 3 disease after platinum chemoradiotherapy in TA1156 (21 May 2026, the LAURA indication), routinely funded from 19 August 2026 | SMC SMC21562019-06-10 Durvalumab accepted under the ultra-orphan and end of life process with PACE (SMC2156, 10 June 2019), three years before NICE. Osimertinib for the same stage 3 setting accepted (SMC2815, 13 April 2026) | Wales: Both NICE appraisals apply. NI: Both NICE appraisals apply. |
| Advanced disease, EGFR mutation-positive (exon 19 deletion or L858R) | Osimertinib alone, osimertinib with pemetrexed and platinum chemotherapy, or amivantamab with lazertinib | NICE TA11222026-01-21 Osimertinib recommended for untreated EGFR mutation-positive disease (TA654, 14 October 2020, the FLAURA indication) and after a first-generation inhibitor in T790M-positive disease (TA653). Osimertinib with pemetrexed and platinum chemotherapy recommended in TA1060 (8 May 2025, the FLAURA2 indication), routinely funded from 5 August 2025. Amivantamab with lazertinib recommended in TA1122 (21 January 2026, the MARIPOSA indication), routinely funded from 21 April 2026. Earlier inhibitors remain options: gefitinib TA192, erlotinib TA258, afatinib TA310, dacomitinib TA595 | SMC SMC28342026-05-11 Osimertinib first line accepted on resubmission under the orphan equivalent process with PACE (SMC2382, 17 January 2022); the FLAURA2 combination accepted (SMC2736, 7 July 2025); amivantamab with lazertinib accepted under the orphan equivalent process with PACE (SMC2834, 11 May 2026) | Wales: All the NICE appraisals apply; every Welsh record for these medicines is marked excluded from AWMSG appraisal because NICE has appraised them. NI: The NICE appraisals apply. |
| Advanced disease, EGFR exon 20 insertion | Amivantamab with carboplatin and pemetrexed, through managed access One of the four lung indications in the Cancer Drugs Fund proper on version 1.408 of the national list. | NICE TA1158 · CDF2026-05-28 Recommended for use during the managed access period, with a managed access agreement, for untreated EGFR exon 20 insertion-positive advanced non-squamous disease; in the Cancer Drugs Fund section of the national list from 8 May 2026 (Blueteq AMI2). Amivantamab monotherapy after platinum chemotherapy was not recommended (TA850, 14 December 2022), and mobocertinib's guidance (TA855, 4 January 2023) has been withdrawn because the marketing authorisation was withdrawn | SMC SMC28782025-12-08 Accepted for routine use on resubmission under the end of life and orphan equivalent process with PACE (SMC2878, 8 December 2025), six months before NICE granted managed access. Amivantamab monotherapy after platinum chemotherapy was not recommended on non-submission (SMC2638, 11 December 2023) | Wales: NICE TA1158 applies, so access is through the Cancer Drugs Fund equivalent arrangements. NI: NICE TA1158 applies. |
| Advanced disease, ALK-positive | Alectinib, brigatinib or lorlatinib first line; lorlatinib or brigatinib after a first inhibitor | NICE TA11032025-10-21 Alectinib (TA536, 8 August 2018), brigatinib (TA670, 27 January 2021), lorlatinib (TA1103, 21 October 2025), ceritinib (TA500, 24 January 2018) and crizotinib (TA406, 28 September 2016) are all recommended for untreated ALK-positive advanced disease; lorlatinib (TA628) and brigatinib (TA571) are recommended after a first inhibitor. Five of the six are routinely funded, lorlatinib first line from 19 January 2026 | SMC SMC24152022-03-07 Alectinib accepted under the orphan medicine process (SMC2012, 13 August 2018); brigatinib accepted on an abbreviated submission (SMC2314, 18 January 2021); lorlatinib accepted first line on an abbreviated submission (SMC2415, 7 March 2022), three and a half years before NICE, and reassessed and accepted for the post-inhibitor setting under the end of life process (SMC2867, 7 September 2026). Ceritinib first line was not recommended in the absence of a submission (1333/18, 9 April 2018), so Scotland has no positive first-line ceritinib advice | Wales: The NICE appraisals apply. NI: The NICE appraisals apply. |
| Advanced disease, ROS1-positive | Crizotinib or entrectinib Repotrectinib, licensed in the European Union for ROS1-positive disease, has no NICE appraisal: NICE discontinued the appraisal on 10 February 2026 after hearing nothing from the company since May 2024. | NICE TA10212024-12-04 Crizotinib recommended for ROS1-positive advanced disease in people who have not had a ROS1 inhibitor, with recommendation 1.2 telling teams to use the least expensive of crizotinib and entrectinib; entrectinib recommended for the same setting in TA643 (12 August 2020). Both routinely funded | SMC SMC22942021-01-18 Entrectinib accepted under the orphan equivalent process with PACE (SMC2294, 18 January 2021); crizotinib accepted for ROS1-positive disease under the ultra-orphan process with PACE (1329/18, 11 June 2018) | Wales: Both NICE appraisals apply. NI: Both NICE appraisals apply. |
| Advanced disease, RET fusion-positive | Selpercatinib | NICE TA10422025-02-19 Selpercatinib recommended for previously treated RET fusion-positive advanced disease (TA1042, 19 February 2025), routinely funded from 20 May 2025; and recommended with managed access for untreated disease (TA911, 26 July 2023), one of the four lung entries in the Cancer Drugs Fund section of the national list, available from 22 June 2023. Pralsetinib was not recommended (TA812, 3 August 2022) and its marketing authorisation was later discontinued | SMC SMC25732023-11-13 Selpercatinib accepted for restricted use in treatment-naive patients on an interim basis subject to reassessment, under the end of life and orphan equivalent process with PACE (SMC2573, 13 November 2023). Its earlier advice for the previously treated setting, not recommended (SMC2371, 8 November 2021), is stated on the newer page to remain valid, so Scotland does not fund what NICE recommends in TA1042 | Wales: Both NICE appraisals apply. NI: Both NICE appraisals apply. |
| Advanced disease, KRAS G12C-mutated, previously treated | Sotorasib, through the Cancer Drugs Fund Adagrasib is the clearest case of a Welsh record being excluded from appraisal on the basis of a NICE appraisal that was terminated, so there is no live positive route in any nation. | NICE TA781 · CDF2022-03-30 Recommended for use within the Cancer Drugs Fund, with a managed access agreement, for KRAS G12C-mutated advanced disease previously treated with at least one systemic therapy; in the Cancer Drugs Fund section of the national list from 3 March 2022 (Blueteq SOT1). The managed access review is in development. Adagrasib's appraisal was terminated on 2 July 2025 because Bristol Myers Squibb will consider restarting when the final overall survival analysis is available | SMC SMC24432022-03-07 Sotorasib accepted on an interim basis subject to reassessment, under the end of life and orphan equivalent process with PACE (SMC2443, 7 March 2022): a different mechanism from the Cancer Drugs Fund with the same effect | Wales: NICE TA781 applies. The Welsh record for sotorasib is marked excluded from AWMSG appraisal pending the managed access review. NI: NICE TA781 applies. |
| Advanced disease, MET exon 14 skipping | Tepotinib | NICE TA7892022-05-18 Recommended within its marketing authorisation for advanced non-small-cell lung cancer with MET exon 14 skipping alterations; routinely funded from 17 June 2022 for both untreated and previously treated disease (Blueteq TEP1 and TEP2). Capmatinib's appraisal was terminated on 3 May 2023 because Novartis did not provide an evidence submission, so tepotinib is the only MET inhibitor funded | SMC SMC25352023-01-16 Accepted on resubmission under the end of life process with PACE (SMC2535, 16 January 2023) | Wales: NICE TA789 applies; capmatinib's Welsh record is excluded from appraisal on the basis of the terminated NICE appraisal TA884. NI: NICE TA789 applies. |
| Advanced disease, BRAF V600-mutated | Encorafenib with binimetinib, or dabrafenib with trametinib, first line | NICE TA11502026-05-06 Encorafenib with binimetinib recommended for BRAF V600E mutation-positive advanced non-small-cell lung cancer, first line only; routinely funded from 4 August 2026 (Blueteq ENC3). Dabrafenib with trametinib recommended for BRAF V600 mutation-positive disease, also first line only (TA898, 14 June 2023), routinely funded from 12 September 2023 | SMC2025-09-08 Encorafenib with binimetinib not recommended in the absence of a submission (SMC2865, 8 September 2025). Scotland's only advice on dabrafenib with trametinib in lung cancer is also a non-submission refusal (1264/17, 10 July 2017). Neither BRAF regimen has a positive Scottish decision | Wales: Both NICE appraisals apply, so Wales funds what Scotland does not. NI: Both NICE appraisals apply. |
| Advanced disease, NTRK fusion-positive | Larotrectinib, through the Cancer Drugs Fund NTRK fusions are rare in lung cancer; they are found on the same comprehensive panel as the commoner drivers. | NICE TA630 · CDF2020-05-27 Recommended for use within the Cancer Drugs Fund, with a managed access agreement, for NTRK fusion-positive solid tumours including lung, where there is no satisfactory alternative; in the Cancer Drugs Fund section of the national list from 21 April 2020 (Blueteq LAR1, whose form asks the clinician to state the histology, for example squamous or non-squamous lung cancer). Entrectinib is no longer an option for NTRK fusions: TA1118 terminated its appraisal on 7 January 2026 because Roche did not provide a complete evidence submission, replacing TA644, though people already taking it continue | Not checked | Wales: NICE TA630 applies. NI: NICE TA630 applies. |
| Advanced disease, no driver, PD-L1 50 percent or more | Pembrolizumab, atezolizumab or cemiplimab, with or without chemotherapy | NICE TA5312018-07-18 Pembrolizumab monotherapy recommended for untreated metastatic disease with a tumour proportion score of 50 percent or more and no EGFR or ALK alteration, stopped at two years (TA531, 18 July 2018). Atezolizumab monotherapy recommended where PD-L1 is on 50 percent or more of tumour cells or 10 percent or more of immune cells (TA705, 2 June 2021). Cemiplimab with platinum-based chemotherapy recommended in TA1165 (16 June 2026) for PD-L1 of 1 percent or more, but only where pembrolizumab with chemotherapy would otherwise be offered | SMC SMC23792021-11-08 Pembrolizumab accepted for restricted use first line at a tumour proportion score of 50 percent or more under the end of life and orphan equivalent process with PACE (1239/17, 10 July 2017). Atezolizumab monotherapy accepted (SMC2379, 8 November 2021). Cemiplimab with chemotherapy was not recommended in the absence of a submission (SMC2724, 7 October 2024), and a monotherapy submission is due on 9 November 2026 | Wales: The NICE appraisals apply, including TA1165, which Scotland does not fund. NI: The NICE appraisals apply. |
| Advanced disease, no driver, PD-L1 below 50 percent | Pembrolizumab with pemetrexed and platinum chemotherapy in non-squamous disease, or with carboplatin and paclitaxel in squamous disease; atezolizumab with bevacizumab and chemotherapy as an alternative in non-squamous disease Nivolumab with ipilimumab and two cycles of chemotherapy was refused in both nations: NICE TA724 (8 September 2021) and SMC2397 (17 January 2022). | NICE TA6832021-03-10 Pembrolizumab with pemetrexed and platinum chemotherapy recommended for untreated metastatic non-squamous disease, stopped at two years, the KEYNOTE-189 indication; routinely funded from 8 June 2021. Pembrolizumab with carboplatin and paclitaxel recommended for untreated metastatic squamous disease in TA770 (9 February 2022). Atezolizumab with bevacizumab, carboplatin and paclitaxel recommended in TA584 (5 June 2019) for untreated non-squamous disease with a tumour proportion score of 0 to 49 percent, or after failure of targeted therapy in driver-positive disease | SMC SMC22072019-10-07 Pembrolizumab with pemetrexed and platinum accepted for restricted use on resubmission under the end of life process with PACE (SMC2207, 7 October 2019); pembrolizumab with carboplatin and paclitaxel accepted for restricted use (SMC2187, 9 September 2019). The atezolizumab combination was not recommended (SMC2208, 11 November 2019), so Scotland does not fund the IMpower150 regimen that England does | Wales: All three NICE appraisals apply. NI: All three NICE appraisals apply. |
| Advanced disease, after chemotherapy | Nivolumab, atezolizumab or pembrolizumab if no prior immunotherapy; docetaxel with nintedanib in adenocarcinoma Erlotinib and gefitinib after chemotherapy are the one place NICE says both yes and no in the same appraisal: TA374 recommends erlotinib in two defined situations, refuses it where the tumour is EGFR-TK mutation-negative and refuses gefitinib outright. | NICE TA7132021-07-07 Nivolumab recommended for advanced non-squamous disease after chemotherapy where PD-L1 is positive, stopped at two years (TA713, 7 July 2021) and for squamous disease after chemotherapy (TA655, 21 October 2020); atezolizumab recommended after chemotherapy (TA520, 16 May 2018); pembrolizumab recommended for PD-L1-positive disease after chemotherapy (TA428, 11 January 2017). Nintedanib with docetaxel recommended in adenocarcinoma only (TA347, 22 July 2015). Ramucirumab with docetaxel was not recommended (TA403, 24 August 2016) and pemetrexed after chemotherapy was not recommended (TA124, 22 August 2007) | SMC2016-10-10 Nivolumab accepted for restricted use in non-squamous disease with a two-year stopping rule (1180/16, 10 October 2016) and accepted for squamous disease (1144/16, 11 July 2016); atezolizumab accepted for restricted use (1336/18, 9 July 2018); pembrolizumab accepted for restricted use (1204/17, 16 January 2017); nintedanib accepted under the end of life and orphan equivalent process with PACE (1027/15, 13 April 2015). Ramucirumab with docetaxel was not recommended on non-submission (1165/16, 13 June 2016), as in England | Wales: The NICE appraisals apply. NI: The NICE appraisals apply. |
| Extensive-stage small-cell lung cancer, first line | Platinum and etoposide with durvalumab, atezolizumab or serplulimab | NICE TA10412025-02-19 Durvalumab with etoposide and either carboplatin or cisplatin recommended for untreated extensive-stage disease in people with an ECOG performance status of 0 or 1, the CASPIAN indication; recommendation 1.3 tells teams to use the least expensive of durvalumab and atezolizumab. Atezolizumab with carboplatin and etoposide recommended in TA638 (1 July 2020, the IMpower133 indication). Serplulimab with carboplatin and etoposide recommended in TA1167 (18 June 2026), routinely funded from 16 September 2026 | SMC SMC27342025-02-10 Durvalumab accepted on an abbreviated submission (SMC2734, 10 February 2025) and atezolizumab accepted under the end of life and orphan process with PACE (SMC2279, 9 November 2020). Serplulimab was not recommended after a full submission with PACE (SMC2840, 19 January 2026), so Scotland does not fund what NICE recommends in TA1167 | Wales: All three NICE appraisals apply. NI: All three NICE appraisals apply. |
| Limited-stage small-cell lung cancer | Cisplatin and etoposide with twice-daily thoracic radiotherapy, then prophylactic cranial irradiation, then durvalumab | NICE TA10992025-10-01 Durvalumab recommended for limited-stage small-cell lung cancer that has not progressed after platinum-based chemoradiotherapy, the ADRIATIC indication; routinely funded from 30 December 2025 (Blueteq DUR7). The chemoradiotherapy itself comes from NG122 recommendations 1.10.1 to 1.10.5, whose twice-daily schedule rests on CONVERT | SMC SMC28182026-05-11 Accepted for use within NHSScotland (SMC2818, 11 May 2026), seven months after NICE: one of the few places on this page where England moved first | Wales: NICE TA1099 applies. NI: NICE TA1099 applies. |
| Relapsed small-cell lung cancer | Oral topotecan, or re-treatment with a platinum-based or anthracycline-containing regimen The bleakest row on the page: in relapsed small-cell disease the NHS funds a 2009 oral chemotherapy and nothing newer, in any of the four nations. | NICE TA1842009-11-25 Oral topotecan recommended only where re-treatment with the first-line regimen is inappropriate and cyclophosphamide, doxorubicin and vincristine is contraindicated; intravenous topotecan is not recommended. Tarlatamab was not recommended after two or more lines including platinum chemotherapy (TA1091, 20 August 2025) and does not appear anywhere in the 320-page national Cancer Drugs Fund list. Lurbinectedin has no published NICE lung appraisal; an appraisal is in development with no date | SMC SMC28162025-11-10 Topotecan capsules accepted for restricted use where first-line re-treatment is inappropriate (545/09, 14 April 2009). Tarlatamab not recommended (SMC2816, 10 November 2025), as in England | Wales: NICE TA184 applies; tarlatamab's Welsh record is excluded from AWMSG appraisal on the basis of the NICE refusal. NI: NICE TA184 applies. |
| Bone metastases | Denosumab to prevent skeletal-related events | NICE TA2652012-10-24 Recommended for preventing skeletal-related events in adults with bone metastases from solid tumours other than prostate cancer, which includes lung cancer | Not checked | Wales: NICE TA265 applies. NI: NICE TA265 applies. |
NICE's lung cancer topic page listed 181 products on the check date, with 66 published technology appraisals and 16 terminated ones. Version 1.408 of the national Cancer Drugs Fund list, updated 24 September 2026 and read in full, carries 43 routinely funded lung indications in its section B and four in the Cancer Drugs Fund proper: amivantamab with carboplatin and pemetrexed (from 8 May 2026), larotrectinib (from 21 April 2020), selpercatinib first line (from 22 June 2023) and sotorasib (from 3 March 2022). Eight lung appraisals are outright refusals: tarlatamab (TA1091), amivantamab monotherapy (TA850), pralsetinib (TA812), nivolumab with ipilimumab and chemotherapy (TA724), necitumumab (TA411), ramucirumab with docetaxel (TA403), erlotinib maintenance (TA227) and pemetrexed after chemotherapy (TA124), with partial refusals inside TA374 and TA184. Sixteen appraisals were terminated, fifteen of them because a company did not provide an evidence submission: entrectinib (TA1118), adagrasib (TA1076), tislelizumab twice (TA1072, TA1058), atezolizumab three times (TA1047, TA618, and in combination), trastuzumab deruxtecan (TA976), capmatinib (TA884), cemiplimab (TA848), durvalumab (TA662), ramucirumab with erlotinib (TA635), afatinib (TA444), alectinib (TA438), bevacizumab twice (TA436, TA148) and nab-paclitaxel (TA362). One appraisal has been withdrawn outright: mobocertinib (TA855), because Takeda stopped marketing the drug. Scotland's register carries 108 lung entries and diverges from England in ten places, six of them medicines England funds and Scotland refuses: serplulimab, perioperative pembrolizumab, perioperative durvalumab, perioperative nivolumab, encorafenib with binimetinib and cemiplimab with chemotherapy, plus no positive advice for dabrafenib with trametinib, first-line ceritinib or previously treated selpercatinib. Scotland was earlier than NICE on adjuvant atezolizumab (by nearly three years), first-line lorlatinib (by three and a half) and first-line amivantamab with chemotherapy, and it alone has a positive decision on oral vinorelbine (179/05, 13 June 2005), which NICE has never appraised. Wales is a NICE-follower for lung cancer: 69 of its 74 lung records are marked excluded from AWMSG appraisal because NICE has appraised the medicine, the only AWMSG-authored outcomes are two statements of advice refusing endorsement after non-submission (afatinib in 2016 and alectinib in 2017), and none of the 28 One Wales interim decisions covers lung cancer. Thirty-two appraisals are in development and 33 awaiting development, including tarlatamab after platinum chemotherapy (expected 13 January 2027), durvalumab with radiotherapy in unresected stage 1 or 2 disease (14 April 2027) and zongertinib for HER2-mutated disease (7 July 2027).
Sources: NICE: all products on lung cancer (181 products on the check date; 66 published technology appraisals and 16 terminated ones). The same address with a page-size parameter answered HTTP 403 (2026-09-25); NHS England: national Cancer Drugs Fund list version 1.408, updated 24 September 2026, read in full (320 pages): four lung indications in the Cancer Drugs Fund section and 43 routinely funded lung indications in section B, each with its Blueteq form, appraisal reference and funding date (2026-09-24); NHS England: national Cancer Drugs Fund list (the page answered HTTP 202 with an empty web application firewall challenge to OnCo on 25 September 2026); NICE TA1091: tarlatamab for extensive-stage small-cell lung cancer after two or more treatments, not recommended (20 August 2025) (2025-08-20); NICE TA1118: entrectinib for NTRK fusion-positive solid tumours in people 12 and over, terminated 7 January 2026 because Roche did not provide a complete evidence submission; it replaces TA644, and people already taking it through the Cancer Drugs Fund continue (2026-01-07); NICE TA855: mobocertinib for EGFR exon 20 insertion-positive advanced non-small-cell lung cancer after platinum chemotherapy (4 January 2023); NICE has withdrawn this guidance because Takeda stopped marketing mobocertinib and its marketing authorisation was withdrawn (2023-01-04); Scottish Medicines Consortium: medicines advice, keyword lung (108 results over six pages on the check date) (2026-09-25); All Wales Therapeutics and Toxicology Centre: medicine recommendations (the keyword search and the results table are loaded by script and returned no rows to OnCo; the 74 lung-cancer records were enumerated from the site's own sitemap) (2026-09-25); All Wales Therapeutics and Toxicology Centre: One Wales medicines, interim decisions (all 28 decisions read; none is for lung cancer) (2026-09-25); NICE: the lung cancer topic page, whose counters give 66 published and 16 terminated technology appraisals, 32 appraisals in development and 33 awaiting development on the check date. The products list answered HTTP 403 whenever a page-size parameter was added to the address (2026-09-25)
The NHS position of every approved product is on the NHS coverage page; the same decisions by country are on HTA decisions.
National Genomic Test Directory entries with their codes, what a result opens, and how the request is made. Ask at diagnosis of advanced disease, not at progression.
| Target | Code | Test | What a positive result opens | How to get it |
|---|---|---|---|---|
| PD-L1 expression (tumour proportion score) | pathology (immunohistochemistry, not in the genomic directory) | Immunohistochemistry on the tumour block, done in the local pathology laboratory at the same time as the slides are prepared for sequencing | Pembrolizumab monotherapy first line at 50 percent or more (TA531), atezolizumab monotherapy at 50 percent of tumour cells or 10 percent of immune cells (TA705), cemiplimab with chemotherapy at 1 percent or more (TA1165), durvalumab after chemoradiotherapy in stage 3 disease at 1 percent or more (TA798), adjuvant atezolizumab at 50 percent or more (TA1071), and combination immunochemotherapy below 50 percent (TA683, TA770) | Reflex: the National Optimal Lung Cancer Pathway has PD-L1 testing and slide preparation for sequencing happening together in local pathology by day 3 after the sample is taken. In Wales, where the audit could count, around a quarter of patients with a recorded result had expression above 50 percent and roughly half had expression below 1 percent Sources: NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); NICE TA531: pembrolizumab for untreated PD-L1-positive metastatic non-small-cell lung cancer (18 July 2018, tumour proportion score of 50 percent or more, stopped at two years; the KEYNOTE-024 indication) (2018-07-18); NICE TA1071: atezolizumab for adjuvant treatment of resected non-small-cell lung cancer (19 June 2025, PD-L1 of 50 percent or more, the IMpower010 indication) (2025-06-19); NLCA blog: what do we know about genomic testing in lung cancer in Wales? (Lauren Dixon for the NLCA project team, 23 June 2026): 745 of 1,546 Welsh patients with a record in the new system had at least one genomic test result (2026-06-23) |
| EGFR (exon 19 deletions, exon 21 L858R, exon 20 insertions, T790M) | M4.1, M4.13 (panel); M4.4 (hotspot tissue), M4.5 (hotspot ctDNA) | Comprehensive next-generation sequencing of DNA and RNA on the tumour block, through a Genomic Laboratory Hub | Osimertinib alone or with chemotherapy and amivantamab with lazertinib in advanced disease (TA654, TA1060, TA1122), adjuvant osimertinib after resection (TA1043), osimertinib after chemoradiotherapy in stage 3 disease (TA1156), and amivantamab with chemotherapy for exon 20 insertions (TA1158). A negative result matters too: it moves you to the immunotherapy rows | Reflex, and mandatory. Version 16 of the National Genomic Test Directory, of 16 July 2026, says testing is indicated for all non-squamous non-small-cell lung cancer and for selected squamous cases with features suggesting a targetable mutation (under 50 and never-smokers), and that the gene targets covered by M4.1 and M4.2 are mandatory to be reported by the Genomic Laboratory Hubs. NG122 recommendation 1.2.12, amended in February 2026, points at the directory for comprehensive next-generation sequencing panels, replacing the earlier single-mutation wording. M4.4, the single-gene EGFR test, is restricted to rare cases where a panel cannot deliver and is subject to close audit. The Welsh audit blog found marked variation between health boards in recorded EGFR results, which it attributes to coding and mapping rather than biology Sources: NHS England: National Genomic Test Directory for cancer, non-central nervous system, version 16.0 of 16 July 2026 (the M4 lung indications and their codes, target genes, technologies and eligibility criteria). The directory's own publication page answers HTTP 202 with an empty body (2026-07-16); NICE NG122: diagnosis and staging (the CT, PET-CT, EBUS-TBNA and sampling recommendations 1.2.1 to 1.2.34, including the multidisciplinary team and the lung cancer clinical nurse specialist) (2026-02); NICE NG122: update information (February 2026 amended recommendation 1.2.12 from single-mutation testing to comprehensive next-generation sequencing panels through genomic laboratory hubs, and added links to the technology appraisals; March 2024 removed the mobocertinib pathways after that guidance was withdrawn) (2026-02); NICE HTG316 (formerly DG9): EGFR-TK mutation testing in adults with locally advanced or metastatic non-small-cell lung cancer (14 August 2013) (2013-08-14); NLCA blog: what do we know about genomic testing in lung cancer in Wales? (Lauren Dixon for the NLCA project team, 23 June 2026): 745 of 1,546 Welsh patients with a record in the new system had at least one genomic test result (2026-06-23) |
| ALK and ROS1 rearrangement | M4.2, M4.13 (panel); M4.6, M4.10 (fluorescence in situ hybridisation), M4.11 (ALK hotspot) | RNA-based next-generation sequencing for fusions on the tumour block; fluorescence in situ hybridisation or immunohistochemistry where there is not enough tissue for sequencing | Alectinib, brigatinib, lorlatinib, ceritinib or crizotinib for ALK (TA536, TA670, TA1103, TA500, TA406) and adjuvant alectinib after resection (TA1014); crizotinib or entrectinib for ROS1 (TA1021, TA643) | Reflex, on the same panel: M4.2 covers ROS1, RET, EML4-ALK and NTRK1, NTRK2 and NTRK3 as structural variants. Both DNA and RNA sequencing should be done in any histological subtype of non-small-cell disease. If tissue runs out, the optimal pathway's salvage route is a limited DNA panel plus fluorescence in situ hybridisation, which the directory carries as its own codes: M4.6 and M4.10 for ROS1 and EML4-ALK. Positives are rare: the Welsh audit found overall prevalence of around 1 to 2 percent for each Sources: NHS England: National Genomic Test Directory for cancer, non-central nervous system, version 16.0 of 16 July 2026 (the M4 lung indications and their codes, target genes, technologies and eligibility criteria). The directory's own publication page answers HTTP 202 with an empty body (2026-07-16); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); NICE NG122: diagnosis and staging (the CT, PET-CT, EBUS-TBNA and sampling recommendations 1.2.1 to 1.2.34, including the multidisciplinary team and the lung cancer clinical nurse specialist) (2026-02); NLCA blog: what do we know about genomic testing in lung cancer in Wales? (Lauren Dixon for the NLCA project team, 23 June 2026): 745 of 1,546 Welsh patients with a record in the new system had at least one genomic test result (2026-06-23); NICE TA1014: alectinib for adjuvant treatment of ALK-positive non-small-cell lung cancer (13 November 2024, stage 1B of 4 cm or larger to 3A; the ALINA indication) (2024-11-13) |
| KRAS G12C, BRAF V600, MET exon 14 skipping, RET fusion, NTRK fusion and HER2 mutation | M4.1 (small variant), M4.2 (structural variant), M4.3 and M4.8 (MET copy number), M4.7 (RET), M4.13 (combined) | The same comprehensive next-generation sequencing panel, reported together | Sotorasib for KRAS G12C through the Cancer Drugs Fund (TA781); encorafenib with binimetinib or dabrafenib with trametinib for BRAF V600, first line only (TA1150, TA898); tepotinib for MET exon 14 skipping (TA789); selpercatinib for RET fusions (TA911 and TA1042); larotrectinib for NTRK fusions through the Cancer Drugs Fund (TA630). A HER2 mutation currently opens nothing: the trastuzumab deruxtecan appraisal was terminated in 2024 and zongertinib's is not expected until July 2027 | All on one reflex request, which is the argument for a comprehensive panel rather than sequential single-gene tests: NICE made exactly that change to NG122 in February 2026. Note what the directory does and does not make essential. KRAS p.(G12C) and MET exon 14 skipping are essential targets on M4.1, so a squamous cancer gets tested for those two even when the full panel is not indicated. HER2 and ERBB2 are not essential targets for any lung indication in version 16: they appear only in the clinical-trials column, to be reported when a panel is already being run for standard-of-care analysis. In small-cell disease the directory offers M231.1, an RB1 copy-number panel for use when the diagnosis cannot be made on morphology or radiology, and M231.2 for NTRK fusions in someone eligible for an NTRK inhibitor Sources: NHS England: National Genomic Test Directory for cancer, non-central nervous system, version 16.0 of 16 July 2026 (the M4 lung indications and their codes, target genes, technologies and eligibility criteria). The directory's own publication page answers HTTP 202 with an empty body (2026-07-16); NICE NG122: update information (February 2026 amended recommendation 1.2.12 from single-mutation testing to comprehensive next-generation sequencing panels through genomic laboratory hubs, and added links to the technology appraisals; March 2024 removed the mobocertinib pathways after that guidance was withdrawn) (2026-02); North Thames Genomic Laboratory Hub: requesting genomic testing in non-small-cell lung cancer (which panel to ask for in squamous against non-squamous disease, and the sample requirements) (2026-09-25); NICE TA781: sotorasib for previously treated KRAS G12C mutation-positive advanced non-small-cell lung cancer (30 March 2022, Cancer Drugs Fund) (2022-03-30); NICE TA789: tepotinib for advanced non-small-cell lung cancer with MET gene alterations (18 May 2022, MET exon 14 skipping) (2022-05-18); NICE TA976: trastuzumab deruxtecan for HER2-mutated advanced non-small-cell lung cancer after platinum-based chemotherapy, terminated 29 May 2024 because Daiichi Sankyo did not provide an evidence submission (2024-05-29) |
| Circulating tumour DNA, when there is not enough tissue or the result is needed sooner | M4.14 (combined ctDNA panel), M4.5 (EGFR hotspot ctDNA) | A blood test sequenced for the same driver mutations, either as a blood predictive biomarker taken at the fast-track clinic before any biopsy, or as salvage after an inadequate sample | The same targeted drugs, sooner. In the NHS pilot of more than 2,500 patients over three years, circulating tumour DNA results came back on average 16 days faster than tissue genotyping, and a health economic analysis estimated savings of around 11 million pounds a year | Ask about it if the biopsy was small or the result is slow. The directory's eligibility for M4.14 is explicit on both uses: radiologically suspected stage 3 or 4 lung cancer unlikely to be suitable for curative treatment with a performance status of 0 to 3, and, separately, a confirmed new diagnosis of non-small-cell lung cancer, previously untreated for advanced disease, where diagnostic molecular testing has failed and the alternative would be to re-biopsy. Its committee note says the blood sample should preferably be taken before the biopsy. M4.5, the single-gene EGFR ctDNA test, is for use when a biopsy is not available at all. Circulating tumour DNA testing was added to the directory in May 2025 and is available to all eligible patients in England, though central procurement of the blood collection kits has ended and trusts now fund them locally. The Genomic Laboratory Hub guidance written by Alastair Greystoke and reviewed by Sanjay Popat and Matthew Krebs tells the clinician how to read the result: green means start the targeted treatment immediately, orange means start standard systemic treatment without waiting for the tissue panel, and red means the sample held too little tumour DNA and you must wait for the tissue result Sources: NHS England: National Genomic Test Directory for cancer, non-central nervous system, version 16.0 of 16 July 2026 (the M4 lung indications and their codes, target genes, technologies and eligibility criteria). The directory's own publication page answers HTTP 202 with an empty body (2026-07-16); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); NHS England: implementation of circulating tumour DNA testing in the NHS (7 April 2026), signed by Sue Hill, Rhydian Phillips and Peter Johnson: ctDNA is commissioned for suspected non-small-cell lung cancer, central kit procurement has ended and trusts now fund the blood collection kits themselves (2026-04-07); North Thames Genomic Laboratory Hub: circulating tumour DNA guidance for clinicians treating patients with advanced lung cancer (page dated 5 March 2026; document authored by Alastair Greystoke, reviewed by Sanjay Popat and Matthew Krebs, version 1.0 approved 7 July 2025), which sets out the green, orange and red result scheme (2026-03-05); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); Newcastle University: Professor Alastair Greystoke (2026-09-25) |
| Enough tissue in the first place | not a test: a pathway rule | Adequate sampling at the first procedure, with additional passes taken specifically for molecular testing | Everything above. This is the step that most often fails | NG122 recommendation 1.2.11 says ensure samples are adequate, without unacceptable risk, to permit pathological diagnosis including tumour subtyping and the assessment of molecular markers, and 1.2.13 says think carefully before doing a test that gives only diagnostic pathology when staging information is also needed. The optimal pathway says to consider taking additional samples for molecular testing at the time of biopsy, and if the tissue is still insufficient the pathologist must email or telephone the lung multidisciplinary team the same day so the team can decide between repeat sampling, which is allowed until day 21, and the salvage route Sources: NICE NG122: diagnosis and staging (the CT, PET-CT, EBUS-TBNA and sampling recommendations 1.2.1 to 1.2.34, including the multidisciplinary team and the lung cancer clinical nurse specialist) (2026-02); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01) |
| Spirometry, transfer factor and cardiopulmonary fitness | pathology and physiology, not genomics | Spirometry and transfer factor before any treatment with curative intent; shuttle walk testing or cardiopulmonary exercise testing where the risk of postoperative breathlessness is moderate or high | Surgery. Fitness, not stage, is what most often decides whether someone with an early cancer is offered an operation: among English patients with stage 1 or 2 disease, 75.3 percent with performance status 0 had surgery against 19.2 percent with performance status 2 | NG122 recommendations 1.4.9 to 1.4.14 set the tests and the thresholds: a shuttle walk of more than 400 m and a maximal oxygen uptake of more than 15 ml/kg/minute count as good function, and people with a predicted postoperative forced expiratory volume or transfer factor below 30 percent should still be offered treatment with curative intent if they accept the risks. The optimal pathway defines routine fitness testing as spirometry, transfer factor, transthoracic echocardiography and, where indicated, a six-minute walk Sources: NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02); NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02) |
The single most useful thing to know about molecular testing in lung cancer in the NHS is the clock, and the second is that nobody publishes whether it is being met. The National Optimal Lung Cancer Pathway gives it 14 calendar days from the moment the sample is taken to a full molecular report in the clinician's hands, with the treating specialist seeing the patient within three working days of the result, which puts the outside limit at 17 days from biopsy; GIRFT asked for ten calendar days, and Roy Castle campaigns for 14 days as something a patient should be able to expect. There is no turnaround column in the test directory and no published national genomic turnaround statistic: NHS England's genomic testing activity release says only activity data has been published and that waiting-time data is planned for a future publication. The last hard numbers are old and bad. The 2019 GIRFT and audit organisational survey found 46 percent of services met the three-day target to a pathological diagnosis and 38 percent met the ten-day target to a molecular result, and the audit's 2020 spotlight on molecular testing, looking at people diagnosed in 2017, found a median of 18 days from tissue acquisition to an EGFR result. The activity itself is now counted: 4,769 lung cancer genomic tests were done nationally in June 2026, from 1,095 in the North Thames Genomic Laboratory Hub to 310 in the South West. But the National Lung Cancer Audit publishes no biomarker testing rates for England at all. A full-text search of its 2026 report for EGFR, ALK, ROS1, PD-L1, molecular, genomic and biomarker returns a single hit, in a recommendation asking trusts to ensure molecular pathology capacity. The only NLCA biomarker data anywhere is a blog about Wales, which found that of 1,546 Welsh patients with a record in the new cancer information system, 745, or 48 percent, had at least one recorded genomic test result. So the NHS mandates a reflex panel, sets a 14-day clock for it, and cannot say what proportion of English patients get either.
Sources: NHS England: National Optimal Lung Cancer Pathway version 4.0, 1 January 2024 (the 49-day maximum to treatment, the direct-to-CT route, the genomic and molecular pathway with its 14-day turnaround, and the timed thoracic surgery and systemic therapy pathways) (2024-01-01); GIRFT: lung cancer, national specialty report (Paul Beckett, Sarah Doffman and Elizabeth Toy, October 2021): 33 recommendations, including an 85 percent radical treatment rate in stage I to II, a surgical resection rate above 20 percent and a ten calendar day turnaround for molecular profiling (2021-10); Roy Castle Lung Cancer Foundation: campaigns (Let Go of the Labels, This is Lung Cancer, and the policy ask that no one should wait longer than 14 days for genomic testing) (2026-09-25); NHS England: National Genomic Test Directory for cancer, non-central nervous system, version 16.0 of 16 July 2026 (the M4 lung indications and their codes, target genes, technologies and eligibility criteria). The directory's own publication page answers HTTP 202 with an empty body (2026-07-16); NHS England: genomic testing activity, quarter 1 of 2026/27, published 11 September 2026 (4,769 lung cancer genomic tests nationally in June 2026, from 1,095 in North Thames to 310 in the South West). The same page says waiting-time data for genomics is not yet published (2026-09-11); NHS Genomics Education Programme, GeNotes: presentation of a patient with advanced non-small-cell lung cancer (last reviewed 7 February 2024, and now past its review date), which says every patient with possible, probable or definite adenocarcinoma suitable for systemic therapy should have molecular testing regardless of smoking status (2024-02-07); National Lung Cancer Audit: State of the Nation 2026, full report (39,409 people in England and 2,135 in Wales diagnosed in 2024; stage, emergency presentation, curative intent, surgery, systemic therapy, times to treatment and survival) (2026-02); NLCA blog: what do we know about genomic testing in lung cancer in Wales? (Lauren Dixon for the NLCA project team, 23 June 2026): 745 of 1,546 Welsh patients with a record in the new system had at least one genomic test result (2026-06-23)
Match a report to targets and drugs on the biomarker matrix.
Registered trials with UK sites, from the ISRCTN registry and the sponsors' pages, with the setting each is for. Eligibility is decided by the trial team.
Sponsor Imperial College London, funded by the NIHR Health Technology Assessment Programme. A de-escalation trial: the question is cost, toxicity and hospital visits, not a new drug.
Registry or sponsor page →Sponsor The Christie, funded by the NIHR and coordinated by Southampton Clinical Trials Unit. Its sister trial QUARTZ LUNG (ISRCTN52137148) asks the same question for people not having systemic treatment.
Registry or sponsor page →Sponsor University of Leeds, funded by Cancer Research UK, the NIHR and AstraZeneca; joint chief investigators Corinne Faivre-Finn and Alastair Greystoke.
Registry or sponsor page →Sponsor University of Oxford, funded by Cancer Research UK and the CRIS Cancer Foundation. The National Cancer Plan names it as the world's first preventative vaccine trial for lung cancer.
Registry or sponsor page →Sponsor University of Manchester, funded by SBRI Healthcare through the NHS Cancer Programme Innovation Call, with Roy Castle Lung Cancer Foundation support. Invitation is by text message from NHS records, then a telephone assessment and a lung health check.
Registry or sponsor page →Sponsor North Bristol NHS Trust, funded by the NIHR. It exists because every UK screening study, from SUMMIT to the Yorkshire Lung Screening Trial, has found uptake lowest among the people at highest risk.
Registry or sponsor page →Sponsor University of Leeds, funded by the NIHR and run from the Leeds Clinical Trials Research Unit.
Registry or sponsor page →Sponsor University of Nottingham, funded by Yorkshire Cancer Research, with Matthew Callister as scientific contact. The UK National Screening Committee recommended screening with integrated smoking cessation, and this is the trial working out what that should be.
Registry or sponsor page →Sponsor University of Birmingham, funded by the NIHR, run from Birmingham Clinical Trials Unit. It is the direct answer to the audit's fifth recommendation for 2026.
Registry or sponsor page →Sponsor Aneurin Bevan University Health Board, funded by Health and Care Research Wales with Amgen, Moondance, Lilly, Illumina, AstraZeneca and Bayer. A whole-nation implementation study, and the reason Wales is the one nation with published lung genomic testing data.
Registry or sponsor page →Sponsor University of Liverpool, funded by UK Research and Innovation and the Medical Research Council.
Registry or sponsor page →Sponsor University of Liverpool, funded by the NIHR and Oxford Cancer Analytics.
Registry or sponsor page →Sponsor University of Cambridge, funded by Yorkshire Cancer Research. The National Cancer Plan calls this moving the scanner down.
Registry or sponsor page →Sponsor the Institute of Cancer Research, funded by Cancer Research UK; also open in France, Italy, Spain and Switzerland.
Registry or sponsor page →Registered on ClinicalTrials.gov rather than ISRCTN; the link is the NIHR Be Part of Research record, because this page cites UK public sources only. Scotland has no national screening programme, so this is how the question is being asked there.
Registry or sponsor page →Sponsor University College London Hospitals. The Be Part of Research record carries only a portfolio number, with no ISRCTN or ClinicalTrials.gov identifier.
Registry or sponsor page →ISRCTN is the UK registry, and its record pages answer HTTP 200 but serve a JavaScript cookie challenge rather than the record, so every trial above was read through the registry's public API. Searches on lung cancer, non-small-cell lung cancer and small-cell lung cancer returned 205, 84 and 105 records; after de-duplication, 158 list a UK recruitment country. The registry split matters for anyone looking for a trial: ISRCTN carries the publicly funded academic portfolio, funded by the NIHR, Cancer Research UK, Yorkshire Cancer Research, the Chief Scientist Office and Health and Care Research Wales, while almost the entire industry portfolio running in UK centres sits on ClinicalTrials.gov and is invisible on ISRCTN. Two of the most important British lung studies have no ISRCTN record at all: TRACERx and SUMMIT. The NIHR's Be Part of Research is the only public place both can be seen together, and it returned 169 recruiting lung cancer studies on the check date. One trial is included here as a failure rather than omitted: RAMON, testing local consolidative treatment in stage 4 disease, is marked Stopped on its own record with 11 people recruited against a target of 244.
Sources: ISRCTN registry, public API (the record pages answer HTTP 200 but serve a cookie challenge, so every trial here was read through the API): 205 records on lung cancer, 84 on non-small-cell and 105 on small-cell, of which 158 list a UK recruitment country (2026-09-25); NIHR Be Part of Research: lung cancer studies recruiting in the UK (169 recruiting studies on the check date; the industry portfolio sits on ClinicalTrials.gov rather than ISRCTN, and Be Part of Research is the only public place a patient can see both) (2026-09-25); NIHR Be Part of Research: TRACERx, which is registered on ClinicalTrials.gov and has no ISRCTN record (2026-09-25); NIHR Be Part of Research: the SUMMIT study, which is registered on ClinicalTrials.gov and has no ISRCTN record (2026-09-25); ISRCTN11613852: RAMON, local consolidative treatment in stage 4 non-small-cell lung cancer (Royal Brompton, NIHR); the record is marked Stopped, with 11 of a target 244 recruited (2026-09-25)
The letter inviting someone to a lung health check is the end of a thirty-year British argument. It began in Liverpool in 1990, when the thoracic surgeon Ray Donnelly, frustrated that patients reached him too late to operate, could not find anyone to fund work on early detection and set up what became the Roy Castle Lung Cancer Foundation to do it himself. Its first grant, in May 1993, paid for work on early genetic changes; in 1999 it paid for the first UK mobile laboratory to recruit high-risk people into screening. Four trials then did the work. Lung-SEARCH, funded by Cancer Research UK, tested the cheap option: annual sputum cytology in 1,568 smokers with chronic obstructive pulmonary disease, with CT only for those whose sputum was abnormal. It failed honestly: sputum sensitivity was 40.5 percent and 55 percent of cancers never appeared in the sputum at all. UKLS, led by John Field from Liverpool, approached 247,354 people and randomised 4,055 selected by the Liverpool Lung Project risk model; 85.7 percent of the cancers it found were stage 1 or 2, and at 7.3 years there were 30 lung cancer deaths in the screened arm against 46. Philip Crosbie's Manchester Lung Health Check pilot then proved the delivery model by parking CT scanners in supermarket car parks in the poorest parts of the city: 75 percent of attendees came from the lowest deprivation quintile, 80 percent of the cancers were early stage, and it cost 10,069 pounds per quality-adjusted life-year. The Liverpool Healthy Lung Programme reached a similar population with similar results. The Yorkshire Lung Screening Trial, run by Matthew Callister and Crosbie with Yorkshire Cancer Research money, then settled the operational questions: which risk rule (PLCOm2012 at 1.51 percent found 91.1 percent of cancers against 62.8 percent for the American categorical rule), what it costs (under 4,100 pounds per quality-adjusted life-year on every rule), and whether stopping smoking can be built into the same appointment (89 percent accepted, 12.4 percent validated quitters at four weeks). SUMMIT, from University College London, took the same model into 329 diverse London practices and found 79.3 percent of its 261 cancers at stage 1 or 2. The UK National Screening Committee recommended targeted screening in June 2022. By the time the National Cancer Plan was published in February 2026, more than 1.5 million people had attended a lung health check, over 9,000 cancers had been found, 76 percent of them at stage 1 or 2 against 30 percent outside the programme, and the early-diagnosis gap between the richest and poorest areas had narrowed by a quarter. Every study also found the same uncomfortable thing: uptake is lowest among current smokers and in the most deprived areas, which is why IMPALA and INSIGHT are now trying to fix it.
Sources: Field JK and others, UK Lung Cancer Screening trial: design and baseline, Health Technology Assessment 2016 (247,354 approached, 4,055 randomised, 42 cancers, 85.7 percent stage 1 or 2) (2016); Field JK and others, UKLS mortality results, Lancet Regional Health Europe 2021 (30 lung cancer deaths against 46, relative rate 0.65; pooled with eight other trials, 0.84) (2021); Crosbie PA and others, implementing lung cancer screening: baseline results from a community Lung Health Check pilot in deprived areas of Manchester, Thorax 2019 (75 percent of attendees in the poorest fifth; 80 percent of the cancers found were early stage) (2019); Ghimire B and others, evaluation of the Liverpool Healthy Lung Programme, Lung Cancer 2019 (more than 80 percent of attenders from the most deprived fifth; 64 percent of cancers stage 1) (2019); Gabe R and others, comparing eligibility criteria in the Yorkshire Lung Screening Trial, Journal of Thoracic Oncology 2025 (the PLCOm2012 risk model at 1.51 percent found 91.1 percent of cancers against 62.8 percent for the 2013 US Preventive Services Task Force rule) (2025); Bhamani A and others, the SUMMIT study baseline round, Lancet Oncology 2025 (12,773 participants from 329 London practices; 79.3 percent of the 261 cancers at stage 1 or 2) (2025); Spiro SG and others, Lung-SEARCH final results, European Respiratory Journal 2019 (1,568 randomised at ten UK centres; no clear stage shift, sputum sensitivity 40.5 percent) (2019); UK National Screening Committee: lung cancer recommendation (June 2022 review): targeted screening with low-dose computed tomography is recommended for people aged 55 to 74 at high risk, with integrated smoking cessation, and the Targeted Lung Health Checks programme is a feasible starting point in England (2022-06); GOV.UK: the National Cancer Plan for England (published 4 February 2026, last updated 15 September 2026): the lung screening roll-out to 2030, the stage shift it has already produced, the narrowing of the early-diagnosis deprivation gap, the 2029 waiting-time targets and the opt-out tobacco dependence offer (2026-02-04); Roy Castle Lung Cancer Foundation: research (the first grant in May 1993; Roy Castle's Tour of Hope raised a million pounds towards the world's first lung cancer research centre, opened May 1998; clinical research fellowships since 2012) (2026-09-25)
British lung cancer trials have a distinctive character: they tend to ask whether a treatment is worth having at all, and they are willing to publish the answer no. CHART is the exception that proves it. Michele Saunders and Stanley Dische at Mount Vernon reasoned that tumour cells repopulate during a six-week radiotherapy course, and built a schedule that gave the whole dose in twelve consecutive days, three fractions a day, weekends included. In 563 patients it cut the relative risk of death by 24 percent and lifted two-year survival from 20 to 29 percent, and in squamous cancers from 19 to 33 percent. The schedule was too demanding for most departments to run, but the principle, that a radiotherapy course should not be allowed to drag, survived it. The Big Lung Trial then tested the 1995 meta-analysis in four settings and found chemotherapy worth nine weeks in advanced disease (hazard ratio 0.77) and worth nothing after surgery or after radical radiotherapy. Its companion paper reported that of 688 newly diagnosed patients at two London centres only 63 entered the trial, and of those potentially eligible, 73.5 percent refused, which is the most honest paragraph in British lung cancer research. QUARTZ, run from the MRC Clinical Trials Unit, randomised 538 people with brain metastases to whole-brain radiotherapy or to supportive care alone and found the radiotherapy added no quality-adjusted survival, a de-implementation result that stopped a routine treatment. CONVERT, led from Manchester by Corinne Faivre-Finn with Cancer Research UK funding, ran 547 patients across 73 centres in eight countries to show that once-daily radiotherapy was better than twice-daily in limited-stage small-cell disease, and did not, which is why NG122 still recommends the twice-daily schedule. VIOLET, from the Royal Brompton, randomised 503 people between keyhole and open lobectomy and found better physical function at five weeks and fewer serious adverse events after discharge, with the same survival: the trial behind the fact that three quarters of English lung resections are now minimally invasive.
Sources: Saunders M and others, continuous hyperfractionated accelerated radiotherapy against conventional radiotherapy in non-small-cell lung cancer, Lancet 1997 (563 patients, 24 percent reduction in the relative risk of death, two-year survival 20 to 29 percent) (1997); Saunders M and others, CHART mature results, Radiotherapy and Oncology 1999 (22 percent reduction in the relative risk of death overall and 30 percent in squamous cancers) (1999); Spiro SG and others, the Big Lung Trial in the supportive care setting, Thorax 2004 (725 randomised; chemotherapy gave a hazard ratio of 0.77 and a median gain of nine weeks) (2004); Spiro SG and others, the difficulty of recruiting to lung cancer trials, Thorax 2000 (of 688 newly diagnosed patients at two London centres only 63, or 9.2 percent, entered the trial) (2000); Mulvenna P and others, QUARTZ, Lancet 2016 (538 patients at 69 UK and three Australian centres; whole-brain radiotherapy added no quality-adjusted survival) (2016); Faivre-Finn C and others, CONVERT, Lancet Oncology 2017 (547 patients; median survival 30 months twice-daily against 25 months once-daily, hazard ratio 1.18, so twice-daily 45 Gy remained the standard) (2017); Lim E and others, VIOLET: video-assisted thoracoscopic or open lobectomy in early-stage lung cancer, NEJM Evidence 2022 (503 randomised; better physical function at five weeks and fewer serious adverse events after discharge with keyhole surgery, same survival at a year) (2022); NICE NG122: management (stop-smoking 1.3.1 to 1.3.3, fitness assessment 1.4, surgery and radiotherapy 1.5, multimodality treatment 1.6 with the perioperative appraisals, small-cell 1.8 to 1.12) (2026-02)
Two British programmes changed what a lung cancer is understood to be, and both were funded by Cancer Research UK. TRACERx, led by Charles Swanton from the UCL Cancer Institute and the Francis Crick Institute with Mariam Jamal-Hanjani as lead clinician, took multiple regions from each resected tumour and sequenced them. The first 100 tumours, across 327 regions, showed that the classic drivers were almost always clonal but that later, scattered drivers were present in more than three quarters of tumours, and that copy-number heterogeneity carried a hazard ratio of 4.9 for recurrence or death. The 421-patient analysis found 22 of 40 common cancer genes under subclonal selection in adenocarcinoma, subclonal whole-genome doubling in 19 percent, and that 8 percent of adenocarcinomas in people with a smoking history carried no tobacco mutational signature and behaved like never-smoker tumours. The PEACE autopsy programme carried the same patients to death: 501 samples from 24 people, covering 70 percent of the metastases visible on imaging, showed that in 62.5 percent of cases several primary subclones disseminated independently and that more than half the metastases sampled had been seeded by other metastases. The same group then showed how lung cancer arises in people who never smoked, finding oncogenic EGFR variants in 18 percent of histologically normal lung tissue and a mechanism by which fine particulate air pollution wakes them up. The National Lung Matrix Trial asked the practical version of the question. Run by Gary Middleton from the Cancer Research UK Clinical Trials Unit in Birmingham across the experimental cancer medicine centre network, it was the largest umbrella trial ever run in lung cancer: 5,467 patients screened, 2,007 molecularly eligible, 302 given genotype-matched therapy across 19 drug-biomarker cohorts. Its 2020 Nature paper said plainly that despite the preclinical rationale only a limited number of combinations showed clinically relevant benefit, and that those were concentrated in cancers associated with minimal tobacco exposure. A later arm reported that vistusertib cannot be recommended in STK11-deficient disease. Between them the two programmes explain why a comprehensive reflex panel is now NHS policy, and why most of the drivers it finds still have nothing to offer.
Sources: Jamal-Hanjani M and others, tracking the evolution of non-small-cell lung cancer, New England Journal of Medicine 2017 (multiregion sequencing of 100 tumours; copy-number heterogeneity carried a hazard ratio of 4.9 for recurrence or death) (2017); Frankell AM and others, the evolution of lung cancer and the impact of subclonal selection in TRACERx, Nature 2023 (1,644 regions from 421 patients; 8 percent of adenocarcinomas in people with a smoking history showed no tobacco mutational signature) (2023); Hessey S and others, evolutionary characterisation of lung cancer metastasis, Nature 2026 (501 samples from 24 people in the PEACE autopsy programme; more than half the metastases sampled were seeded by other metastases) (2026); Hill W and others, lung adenocarcinoma promotion by air pollutants, Nature 2023 (particulate matter and EGFR-driven lung cancer across 32,957 cases; oncogenic EGFR variants found in 18 percent of histologically normal lung samples) (2023); Middleton G and others, the National Lung Matrix Trial of personalised therapy in lung cancer, Nature 2020 (5,467 screened, 2,007 molecularly eligible, 302 treated across 19 drug-biomarker cohorts) (2020); Middleton G and others, a phase 2 trial of mTORC1/2 inhibition in STK11-deficient non-small-cell lung cancer, npj Precision Oncology 2025 (vistusertib cannot be recommended in this setting) (2025)
Each figure with its nation, period and the page it was read from. Survival figures are population averages and sit behind the usual disclosure.
The third most common cancer, 11 percent of all new cases, nearly 140 a day: around 25,500 in males and 24,700 in females. Rates are highest at ages 80 to 84, and 46 percent of cases are in people aged 75 and over.
Sources: Cancer Research UK: lung cancer incidence (2026-09-25)
The most common cause of cancer death in the UK, 90 a day; 54 percent in people aged 75 and over. Rates are down 40 percent since the early 1970s and 22 percent in the last decade. An estimated 668,000 lung cancer deaths were avoided in the UK by 2021.
Sources: Cancer Research UK: lung cancer mortality (the deprivation gradient in mortality and the deaths linked with deprivation) (2026-09-25)
Averages across everyone diagnosed, often years ago. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Sources: Cancer Research UK: lung cancer survival (including five-year survival by deprivation group in England) (2026-09-25)
The steepest deprivation gradient of any common cancer. Around 13,400 lung cancer deaths a year in the UK are linked with deprivation, around 6,500 in females and 6,900 in males.
Sources: Cancer Research UK: lung cancer mortality (the deprivation gradient in mortality and the deaths linked with deprivation) (2026-09-25)
Averages across everyone diagnosed, often years ago. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Sources: Cancer Research UK: lung cancer survival (including five-year survival by deprivation group in England) (2026-09-25)
The steepest gradient of any cancer site in Public Health Scotland's workbook, and it has widened: the ratio was 2.97 for 2015 to 2019. In absolute terms 7,772 lung cancers arose in the most deprived fifth over five years against 3,104 in the least. Scotland's own cancer strategy puts it in one line: lung cancer is three times more common in the most deprived areas than the least.
Sources: Public Health Scotland: cancer incidence by deprivation, table 3 (trachea, bronchus and lung, SIMD quintiles, 2020 to 2024: 165.8 per 100,000 in the most deprived fifth against 52.4 in the least) (2026-08-18)
Also widening, from 3.09 in 2015 to 2019. Public Health Scotland attributes part of Scotland's overall cancer mortality gap to the greater likelihood of developing cancers with low survival, naming lung cancer.
Sources: Public Health Scotland: cancer mortality by deprivation, table 5 (trachea, bronchus and lung, 2020 to 2024: 123.1 per 100,000 in the most deprived fifth against 34.9 in the least) (2026-07-14)
A most-to-least ratio of about 2.44. Over the five years, 1,775 cases arose in the most deprived fifth against 982 in the least.
Late-stage incidence in the most deprived areas was 2.6 times the late-stage rate in the least deprived, so the gap is wider for advanced disease than for early disease.
One disease accounting for roughly a ninth of the entire socioeconomic life expectancy gap.
71 percent from active smoking and 1 percent from environmental tobacco smoke; 79 percent of UK lung cancer cases are preventable in total. Occupational exposures account for 13 percent, outdoor air pollution 8 percent and ionising radiation 5 percent.
Sources: Cancer Research UK: lung cancer risk factors (the preventable fraction and the smoking attributable fraction) (2026-09-25)
Across 123 English NHS trusts. For the first time more women than men were diagnosed: 50.8 percent female. Median age 74.0 years. Small-cell disease was 6.6 percent of English cases, down from 8.6 percent in 2019.
England was 32 percent in 2022 and 35.5 percent in 2023: the fastest stage shift in any common cancer, and the audit attributes it to screening. Stage 4 fell from 47 percent in 2022 to 41 percent in 2024.
The NHS Lung Cancer Screening Programme reported 7,329 cancers among people aged 55 to 74 invited over this period, of which 3,175 were in 2024 to 2025 alone. The proportion at stage 1 or 2 ranged from 63 to 81 percent between cancer alliances.
Down from 33 percent in England in 2022, but the audit says the screening programme's effect has not yet translated into fewer emergency presentations.
The registry's own comparison for 2018 to 2020 put Northern Ireland at 40.5 percent against England's 33.7 percent. One-year net survival was 22.9 percent for this route against 61.6 percent for the other-outpatient route.
Up from 19.6 percent in England in 2023 and 18 percent in 2022; the absolute number of people receiving curative treatment rose from 5,561 in 2019 to 8,936 in 2024, an increase of more than 60 percent. Resection rates range from 15 to 37 percent between cancer alliances.
Only 12 percent of English patients were operated on within 49 days. For radical radiotherapy the median was 98 days and 3.2 percent met the target; for systemic therapy in stage 3B to 4 disease, 63 days and 27 percent.
Averages across everyone diagnosed, often years ago. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Averages across everyone diagnosed, often years ago. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Sources: Public Health England: adult cancer survival data tables (lung, England, diagnosed 2014 to 2018: five-year age-standardised net survival 58.7 percent at stage 1 against 3.4 percent at stage 4) (2020-11-05)
Averages across everyone diagnosed, often years ago. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
Averages across everyone diagnosed, often years ago. Your stage, subtype, age, fitness and the treatment you receive matter more than the average, and the numbers are improving quickly.
European age-standardised rate 89.1 per 100,000, down from 98.1 in 2022. Lung cancer rates fell 23 percent in males and 7 percent in females over the decade to 2024.
Sources: Public Health Scotland open data: cancer incidence at Scotland level (trachea, bronchus and lung, ICD-10 C33-C34: 5,200 cases in 2024) (2026-08-18)
The most common cause of cancer death in Scotland, 22.3 percent of all cancer deaths, at a European age-standardised rate of 62.8 per 100,000.
Sources: Public Health Scotland: cancer mortality, annual update to 2024 (published 14 July 2026): 3,651 lung cancer deaths in Scotland in 2024, 22.3 percent of all cancer deaths (2026-07-14)
Of the 4,784 cases with a known stage, 34.3 percent were stage I or II. One-year net survival rose from 40.8 percent for 2013 to 2017 to 45.7 percent for 2018 to 2022, and five-year from 16.4 to 19.9 percent.
Sources: Public Health Scotland: trends in cancer staging, table 9 (lung, Scotland 2024: 24.6 percent stage I, 41.1 percent stage IV) (2026-08-18)
6,845 cases over the five years, 48.5 percent in women; 13.0 percent of all cancers in both sexes. Median age at diagnosis 73. 94.7 percent had a stage assigned, the best stage completeness of the four nations, with 20.2 percent stage I and 44.6 percent stage IV.
22.6 percent of all male and 21.8 percent of all female cancer deaths. At the end of 2023, 2,964 people diagnosed since 1999 were alive.
Of 9,053 cancer deaths in Wales in 2025, lung cancer was the largest single cause. All-cancer death rates were 54 percent higher in the most deprived fifth than the least.
Sources: Welsh Cancer Intelligence and Surveillance Unit: cancer mortality in Wales (published 15 July 2026): lung cancer causes two in every ten cancer deaths in Wales (2026-07-15)
Lung cancer caused more than twice as many deaths as the next most lethal category while receiving less funding than four other cancer types. The authors attribute the gap to a blame-the-victim attitude. No more recent UK-wide figure could be found on a public UK page.
Charities focused on this cancer, the general cancer charities, and the official schemes that help with costs. Each link goes to the organisation's own page.
More schemes by country on Assistance; costs of care on Costs.
Where England, Scotland, Wales and Northern Ireland run different rules for the same step.
Named gaps, so a missing figure is never mistaken for a zero.