Contrast-enhanced mammography reduces costs per QALY in breast cancer screening recalls compared to conventional imaging
This randomized controlled trial included women recalled from breast cancer screening in a hospital perspective setting. The study compared contrast-enhanced mammography (CEM) as the primary tool against conventional imaging. The primary outcome measured costs per quality-adjusted life year (QALY). Secondary outcomes included total costs, average imaging costs, and health-related quality of life assessed with EQ-5D-5L. The follow-up duration was 18.0 months.
Results indicated lower total costs with an effect size of €-117 and a 95% CI of €-254; €+22. Average imaging costs were significantly lower with an effect size of €-130 and a 95% CI of €-153; €-105. Mean QALYs were 1.2034 for CEM versus 1.2137 for conventional imaging. The probability of cost-effectiveness was 53% at a threshold of €10,000. In the BI-RADS 0 subgroup, the probability of cost-effectiveness was 85%.
Safety and tolerability data were not reported. No adverse events, serious adverse events, or discontinuations were documented in the provided data. Missing data were handled with multiple imputation, and uncertainty was examined with non-parametric bootstrap analysis. Funding or conflicts of interest were not reported.
In BI-RADS-0 recalls, CEM should be used as the primary imaging modality instead of conventional imaging. In other recalls, CEM should be strongly considered. The evidence is limited by the lack of reported safety outcomes and missing data handling methods.