Do type 1 receptor tyrosine kinases inform treatment choice? A prospectively planned analysis of the TEAM trial
British Journal of Cancer , Volume 109 - Issue 9 p. 2453- 2461
Background:Epidermal growth factor receptors contribute to breast cancer relapse during endocrine therapy. Substitution of aromatase inhibitors (AIs) may improve outcomes in HER-positive cancers.Methods:Tissue microarrays were constructed. Quantitative analysis of HER1, HER2, and HER3 was performed. Data were analysed relative to disease-free survival and treatment using outcomes at 2.75 and 6.5 years.Results:Among 4541 eligible samples, 4225 (93%) had complete HER1-3 data. Overall, 5% were HER1-positive, 13% HER2-positive, and 21% HER3-positive; 32% (n=1351) overexpressed at least one HER receptor. In the HER1-3-negative subgroup, the hazard ratio (HR) for upfront exemestane vs tamoxifen at 2.75 years was 0.67 (95% confidence interval (CI), 0.52-0.87), in the HER1-3-positive subgroup, the HR was 1.15 (95% CI, 0.85-1.56). A prospectively planned treatment-by-marker analysis demonstrated a significant interaction between HER1-3 and treatment at 2.75 years (HR=0.58; 95% CI, 0.39-0.87; P=0.008), as confirmed by multivariate regression analysis adjusting for prognostic factors (HR=0.55; 95% CI, 0.36-0.85; P=0.005). This effect was time dependent.Conclusion:In the 2.75 years prior to switching patients initially treated with tamoxifen to exemestane, a significant treatment-by-marker effect exists between AI/tamoxifen treatment and HER1-3 expression, suggesting HER expression could be used to select appropriate endocrine treatment at diagnosis to prevent or delay early relapses.
|early breast cancer, exemestane, HER1/EGFR, HER2, HER3, oestrogen receptor, tamoxifen|
|British Journal of Cancer|
|Organisation||Department of Medical Oncology|
Bartlett, J.M.S, Brookes, C.L, Piper, T, van de Velde, C.J.H, Stocken, D.D, Lyttle, N, … Rea, D. (2013). Do type 1 receptor tyrosine kinases inform treatment choice? A prospectively planned analysis of the TEAM trial. In British Journal of Cancer (Vol. 109, pp. 2453–2461). doi:10.1038/bjc.2013.609