RT Journal Article SR Electronic T1 International differences in lung cancer survival by sex, histological type and stage at diagnosis: an ICBP SURVMARK-2 Study JF Thorax JO Thorax FD BMJ Publishing Group Ltd and British Thoracic Society SP 378 OP 390 DO 10.1136/thoraxjnl-2020-216555 VO 77 IS 4 A1 Araghi, Marzieh A1 Fidler-Benaoudia, Miranda A1 Arnold, Melina A1 Rutherford, Mark A1 Bardot, Aude A1 Ferlay, Jacques A1 Bucher, Oliver A1 De, Prithwish A1 Engholm, Gerda A1 Gavin, Anna A1 Kozie, Serena A1 Little, Alana A1 Møller, Bjørn A1 St Jacques, Nathalie A1 Tervonen, Hanna A1 Walsh, Paul A1 Woods, Ryan A1 O'Connell, Dianne L A1 Baldwin, David A1 Elwood, Mark A1 Siesling, Sabine A1 Bray, Freddie A1 Soerjomataram, Isabelle A1 ICBP SURVMARK-2 Local Leads A1 ICBP SURVMARK-2 Academic Reference Group A1 YR 2022 UL http://thorax.bmj.com/content/77/4/378.abstract AB Introduction Lung cancer has a poor prognosis that varies internationally when assessed by the two major histological subgroups (non-small cell (NSCLC) and small cell (SCLC)).Method 236 114 NSCLC and 43 167 SCLC cases diagnosed during 2010–2014 in Australia, Canada, Denmark, Ireland, New Zealand, Norway and the UK were included in the analyses. One-year and 3-year age-standardised net survival (NS) was estimated by sex, histological type, stage and country.Results One-year and 3-year NS was consistently higher for Canada and Norway, and lower for the UK, New Zealand and Ireland, irrespective of stage at diagnosis. Three-year NS for NSCLC ranged from 19.7% for the UK to 27.1% for Canada for men and was consistently higher for women (25.3% in the UK; 35.0% in Canada) partly because men were diagnosed at more advanced stages. International differences in survival for NSCLC were largest for regional stage and smallest at the advanced stage. For SCLC, 3-year NS also showed a clear female advantage with the highest being for Canada (13.8% for women; 9.1% for men) and Norway (12.8% for women; 9.7% for men).Conclusion Distribution of stage at diagnosis among lung cancer cases differed by sex, histological subtype and country, which may partly explain observed survival differences. Yet, survival differences were also observed within stages, suggesting that quality of treatment, healthcare system factors and prevalence of comorbid conditions may also influence survival. Other possible explanations include differences in data collection practice, as well as differences in histological verification, staging and coding across jurisdictions.Data may be obtained from a third party and are not publicly available. Data contain sensitive and personal information and can be obtained from the cancer registries listed as the local leads in the manuscript.