作者
Sheryl M. Gough,Jean Flanagan,Jessica L.F. Teh,Monica Andreoli,Emma Rousseau,Melissa Pannone,Mark Bookbinder,Ryan Willard,Kim Davenport,Elizabeth Bortolon,Gregory Cadelina,Debbie Gordon,Jennifer Pizzano,Jennifer Macaluso,Leofal Soto,John Corradi,Katherine Digianantonio,Ieva Drulyte,Alicia Morgan,Connor Quinn,Miklós Békés,Caterina Ferraro,Xin Chen,Gan Wang,Hanqing Dong,Jing Wang,David R. Langley,John Houston,Richard Gedrich,I Taylor
摘要
Estrogen Receptor (ER) alpha signaling is a known driver of ER-positive (ER+)/human epidermal growth factor receptor 2 negative (HER2-) breast cancer. Combining endocrine therapy (ET) such as fulvestrant with CDK4/6, mTOR or PI3K inhibitors is now a central strategy for the treatment of ER+ advanced breast cancer. However, suboptimal ER inhibition and resistance resulting from ESR1 mutation dictates that new therapies are needed.