Drug Resistance in HER2-Positive Breast Cancer Brain Metastases: Blame the Barrier or the Brain?

被引:70
|
作者
Kabraji, Sheheryar [1 ,2 ]
Ni, Jing [2 ,3 ]
Lin, Nancy U. [1 ]
Xie, Shaozhen [2 ,3 ]
Winer, Eric P. [1 ]
Zhao, Jean J. [2 ,3 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA USA
关键词
CELL LUNG-CANCER; LAPATINIB PLUS CAPECITABINE; PI3K PATHWAY; PHASE-II; ANTITUMOR-ACTIVITY; KINASE INHIBITOR; TRASTUZUMAB; MULTICENTER; NERATINIB; THERAPY;
D O I
10.1158/1078-0432.CCR-17-3351
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The brain is the most common site of first metastasis for patients with HER2-positive breast cancer treated with HER2-targeting drugs. However, the development of effective therapies for breast cancer brain metastases (BCBM) is limited by an incomplete understanding of the mechanisms governing drug sensitivity in the central nervous system. Pharmacodynamic data from patients and in vivo models suggest that inadequate drug penetration across the "blood-tumor" barrier is not the whole story. Using HER2-positive BCBMs as a case study, we highlight recent data from orthotopic brain metastasis models that implicate brain-specific drug resistance mechanisms in BCBMs and suggest a translational research paradigm to guide drug development for treatment of BCBMs. (C) 2018 AACR.
引用
收藏
页码:1795 / 1804
页数:10
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