4.7 Article

Five ways to improve international comparisons of cancer survival: lessons learned from ICBP SURVMARK-2

Journal

BRITISH JOURNAL OF CANCER
Volume 126, Issue 8, Pages 1224-1228

Publisher

SPRINGERNATURE
DOI: 10.1038/s41416-022-01701-0

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Funding

  1. Canadian Partnership Against Cancer
  2. Cancer Council Victoria
  3. Cancer Institute New South Wales
  4. Cancer Research UK
  5. Danish Cancer Society
  6. National Cancer Registry Ireland
  7. Cancer Society of New Zealand
  8. NHS England
  9. Norwegian Cancer Society
  10. Public Health Agency Northern Ireland on behalf of the Northern Ireland Cancer Registry
  11. DG Health and Social Care, Scottish Government
  12. Western Australia Department of Health
  13. Public Health Wales NHS Trust
  14. Karolinska Institute

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This study examines the comparison of population-based cancer survival rates internationally and aims to improve the harmonization of cancer registry datasets for future benchmarking exercises. It emphasizes the importance of understanding and addressing international variations in outcomes among cancer patients.
Background Comparisons of population-based cancer survival between countries are important to benchmark the overall effectiveness of cancer management. The International Cancer Benchmarking Partnership (ICBP) Survmark-2 study aims to compare survival in seven high-income countries across eight cancer sites and explore reasons for the observed differences. A critical aspect in ensuring comparability in the reported survival estimates are similarities in practice across cancer registries. While ICBP Survmark-2 has shown these differences are unlikely to explain the observed differences in cancer-specific survival between countries, it is important to keep in mind potential biases linked to registry practice and understand their likely impact. Methods Based on experiences gained within ICBP Survmark-2, we have developed a set of recommendations that seek to optimally harmonise cancer registry datasets to improve future benchmarking exercises. Results Our recommendations stem from considering the impact on cancer survival estimates in five key areas: (1) the completeness of the registry and the availability of registration sources; (2) the inclusion of death certification as a source of identifying cases; (3) the specification of the date of incidence; (4) the approach to handling multiple primary tumours and (5) the quality of linkage of cases to the deaths register. Conclusion These recommendations seek to improve comparability whilst maintaining the opportunity to understand and act upon international variations in outcomes among cancer patients.

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