Araghi, M.et al | 2021| International differences in lung cancer survival by sex, histological type and stage at diagnosis: an ICBP SURVMARK-2 Study| Thorax | Published Online First: 19 July 2021| doi: 10.1136/thoraxjnl-2020-216555
The authors of this study set out to answer the following research question: Are there international disparities in lung cancer survival by clinically relevant subgroups in the most recent population-level data?
In this paper, they present their in-depth results of the most up-to-date differences of lung cancer stage distribution and survival by histological types, age group and sex for each included country, as well as within countries, followed by a discussion of potential causes of the disparities including clinical and data factors.
Abstract
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 per cent for the UK to 27.1 per cent 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 per cent for women; 9.1 per cent for men) and Norway (12.8 per cent for women; 9.7 per cent 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.
Full paper is available from Thorax