作者
Komal Jhaveri,L.D. Eli,Hans Wildiers,Sara A. Hurvitz,Ángel Guerrero-Zotano,Nisha Unni,Adam Brufsky,H. Park,James Waisman,En‐Hua Yang,Iben Spanggaard,Sonya Reid,Mark E. Burkard,Shaveta Vinayak,Aleix Prat,Mónica Arnedos,François‐Clément Bidard,Sherene Loi,John Crown,Manali Bhave,Sarina A. Piha‐Paul,Jennifer M. Suga,Stephen Chia,Cristina Saura,José Á. García-Sáenz,Valentina Gambardella,Maria J. de Miguel,Einav Nili Gal‐Yam,A. Raphael,Salomon M. Stemmer,X. Cynthia,Ariella B. Hanker,D. Ye,Jonathan W. Goldman,Ron Bose,Lanell M. Peterson,Joshua S. K. Bell,A. Lindsay Frazier,D. DiPrimeo,Alvin Wong,Carlos L. Arteaga,David B. Solit
摘要
HER2 mutations are targetable alterations in patients with hormone receptor-positive (HR+) metastatic breast cancer (MBC). In the SUMMIT basket study, patients with HER2-mutant MBC received neratinib monotherapy, neratinib + fulvestrant, or neratinib + fulvestrant + trastuzumab (N + F + T). We report results from 71 patients with HR+, HER2-mutant MBC, including 21 (seven in each arm) from a randomized substudy of fulvestrant versus fulvestrant + trastuzumab (F + T) versus N + F + T.