PI3K pathway activation (defined by a PIK3CA/ERBB mutation and/or low expression of PTEN) was found in 25 (55.6%) tumours overall and was not influenced by either ER or PR status: 57.9% of ER-negative tumours and 53.8% of ER-positive tumours had an activated PI3K pathway, whereas 58.6% of PR-negative and 50% of PR-positive tumours had an activated PI3K pathway. This evidence concerns the gene PGR and neoplasm.