作者
Lei Fan,Zhonghua Wang,Linxiaoxi Ma,Song‐Yang Wu,Jiong Wu,Ke‐Da Yu,Xin-Yi Sui,Ying Xu,Xiyu Liu,Li Chen,Wenjuan Zhang,Xi Jin,Qin Xiao,Ruohong Shui,Yi Xiao,Han Wang,Yun‐Song Yang,Xiaoyan Huang,A‐Yong Cao,Junjie Li,Gen‐Hong Di,Guang-Yu Liu,Wentao Yang,Xin Hu,Yan Xia,Qiannan Liang,Yi‐Zhou Jiang,Zhi‐Ming Shao
摘要
Triple-negative breast cancers display heterogeneity in molecular drivers and immune traits. We previously classified triple-negative breast cancers into four subtypes: luminal androgen receptor (LAR), immunomodulatory, basal-like immune-suppressed (BLIS), and mesenchymal-like (MES). Here, we aimed to evaluate the efficacy and safety of subtyping-based therapy in the first-line treatment of triple-negative breast cancer.