Estrogen-Receptor Loss and Mutation in Estrogen-Receptor-Positive Metastatic Breast Cancer and the Effect on Overall Survival

In patients with metastatic estrogen-receptor (ER)-positive HER2-negative breast cancer, the loss of ER expression and the mutation of -the gene encoding the ER receptor-are mechanisms for resistance to endocrine therapy. We aimed to determine the frequency of these mechanisms and their interaction. Metastases were retrieved from our pathology files. hotspot mutations resulting in p.(D538G), p.(Y537S), and p.(L536H) were determined by means of pyrosequencing. Clinical data were retrieved from electronic medical records. A total of 136 metastases were available for analysis. ER loss was found in 23 metastases (17%). mutations were found in 18 metastases (13%), including p.(D538G) in 9, p.(Y537S) in 7, and p.(L536H) in 2. mutation and ER loss were mutually exclusive ( = 0.042), and mutation was associated with endocrine therapy ( = 0.002). mutation was found in two primary breast cancers. mutations are rare in primary breast cancer and develop in metastases during endocrine therapy. Furthermore, ER loss had a statistically significant negative effect on overall survival when compared to patients without ER loss, with a rate ratio of 3.21 (confidence interval 1.95-5.26). No such effect was observed for mutations, with a rate ratio of 1.15 (confidence interval 0.67-1.95). We conclude that ER loss and mutation together account for 30% of the resistance to endocrine therapy.