Abstract
Trastuzumab has conferred significant clinical benefits in HER-2-positive breast carcinomas. HER-2 status is determined by immunohistochemistry (IHC) and/or fluorescence in situ hybridisation (FISH), but appropriate assessment of HER2 status remains subject to considerable debate. Data on the health economic impact of HER-2 test strategies are limited. A life-long Markov state transition model was used to assess costs and effectiveness of HER-2 assay strategies (based on IHC, FISH, both combined or FISH confirmation of IHC2+) for a hypothetical cohort of early breast cancer patients from the perspective of the Swiss health system. We compared clinically relevant strategies of predictive testing and subsequent trastuzumab treatment of HER-2-positive patients only. FISH testing was the most cost–effective strategy with an incremental cost–effectiveness ratio of €12,245 per additional quality-adjusted life-year (QALY) gained, compared to no trastuzumab treatment. The next best strategy was parallel IHC and FISH, with costs of €400,154/QALY gained compared to FISH alone. FISH as primary HER-2 testing modality remained the preferred option in deterministic and probabilistic sensitivity analysis. Predictive testing to identify adjuvant breast cancer patients who benefit from trastuzumab treatment is a clinical and economic necessity. Our model identifies FISH as the most cost–effective approach.
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Acknowledgement
We thank KJ Dedes, Department of Obstetrics and Gynaecology and BC Pestalozzi, Department of Oncology, University Hospital Zurich, Switzerland for commenting on clinical issues.
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No conflict of interest to declare.
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This work was supported by an unrestricted educational grant of the ETH Zurich Foundation and the Competence Center for Systems Physiology and Metabolic Diseases (CC-SPMD), Zurich, Switzerland.
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Blank, P.R., Schwenkglenks, M., Moch, H. et al. Human epidermal growth factor receptor 2 expression in early breast cancer patients: a Swiss cost–effectiveness analysis of different predictive assay strategies. Breast Cancer Res Treat 124, 497–507 (2010). https://doi.org/10.1007/s10549-010-0862-7
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DOI: https://doi.org/10.1007/s10549-010-0862-7