We have chosen to perform this analysis without previously classifying tumours according to immunohistochemical phenotype (luminal (A and B), HER2, basal (triple-negative: ER-, PR-, HER-) and unclassified) because, in our cohort, the low number of tumours in each immunohistochemical phenotype did not allow us to perform CR and Kaplan-Meier log-rank analyses to investigate p53 isoform expression in relation to clinical outcome. This evidence concerns the gene TP53 and neoplasm.