4.6 Article

Extending Age Ranges in Breast Cancer Screening in Four European Countries: Model Estimations of Harm-to-Benefit Ratios

Journal

CANCERS
Volume 13, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13133360

Keywords

breast cancer screening; harm-to-benefit ratios; microsimulation; overdiagnosis; breast cancer deaths averted; false-positive results

Categories

Funding

  1. EU-Framework Programme (Horizon 2020) of the European Commission [634753]
  2. H2020 Societal Challenges Programme [634753] Funding Source: H2020 Societal Challenges Programme

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Breast cancer screening can both benefit and harm, with age playing a role in the balance between the two. A study using microsimulation modeling compared different age ranges of screening in four European countries to evaluate harm-to-benefit ratios. Adapting the age range of screening is a potential option to improve harm-to-benefit ratios, with the prioritization of considered harms and benefits impacting interpretation of results.
Simple Summary Breast cancer screening causes harms and benefits. The balance between the two varies by age. By applying microsimulation modelling, we compared several age ranges of screening in four European countries (the Netherlands, Finland, Italy and Slovenia) and evaluated the respective harm-to-benefit ratios. In all countries, adding screening between the ages 45 and 49 or 70 and 74 resulted in more life-years gained and more breast cancer deaths averted, but at the expense of increases in harms. Adapting the age range of breast cancer screening is an option to improve harm-to-benefit ratios in all four countries. The prioritization of considered harms and benefits affects the interpretation of results. The main benefit of breast cancer (BC) screening is a reduction in mortality from BC. However, screening also causes harms such as overdiagnosis and false-positive results. The balance between benefits and harms varies by age. This study aims to assess how harm-to-benefit ratios of BC screening vary by age in the Netherlands, Finland, Italy and Slovenia. Using microsimulation models, we simulated biennial screening with 100% attendance at varying ages for cohorts of women followed over a lifetime. The number of overdiagnoses, false-positive diagnoses, BC deaths averted and life-years gained (LYG) were calculated per 1000 women. We compared four strategies (50-69, 45-69, 45-74 and 50-74) by calculating four harm-to-benefit ratios, respectively. Compared to the reference strategy 50-69, screening women at 45-74 or 50-74 years would be less beneficial in any of the four countries than screening women at 45-69, which would result in relatively fewer overdiagnoses per death averted or LYG. At the same time, false-positive results per death averted would increase substantially. Adapting the age range of BC screening is an option to improve harm-to-benefit ratios in all four countries. Prioritization of considered harms and benefits affects the interpretation of results.

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