作者: Takeo Fujii , Naoko Matsuda , Miho Kono , Kenichi Harano , Huiqin Chen
DOI: 10.1016/J.EJCA.2017.11.015
关键词: Metastatic breast cancer 、 Multivariate analysis 、 High rate 、 Somatic cell 、 Gene profile 、 Internal medicine 、 Medicine 、 Breast cancer 、 Systemic therapy 、 Oncology 、 Pik3ca mutation
摘要: Abstract Background Understanding the biology of breast cancer is important for guiding treatment strategies and revealing resistance mechanisms. Our objectives were to investigate relationship between previous systemic therapy exposure mutational spectrum in metastatic identify clinicopathological factors associated with identified frequent somatic mutations. Methods Archival tissues patients subjected hotspot molecular testing by next-generation sequencing. The variables that significantly differed (P Results A total 922 included analysis. In multivariate analysis, before (N = 186) was a higher rate TP53 PIK3CA mutations compared lack Conclusion Systemic an independent risk factor high rates mutation, which suggests importance samples after accurately assess It worth gene profile when tumours become resistant treatments.