Preclinical and Clinical Efficacy of Trastuzumab Deruxtecan in Breast Cancer Brain Metastases

被引:53
|
作者
Kabraji, Sheheryar [1 ]
Ni, Jing [1 ]
Sammons, Sarah [2 ]
Li, Tianyu [1 ]
Van Swearingen, Amanda E. D. [2 ]
Wang, Yanzhi [1 ]
Pereslete, Alyssa [1 ]
Hsu, Liangge [3 ]
DiPiro, Pamela J. [3 ]
Lascola, Chris [2 ]
Moore, Heather [2 ]
Hughes, Melissa [1 ]
Raghavendra, Akshara S. [4 ]
Gule-Monroe, Maria [4 ]
Murthy, Rashmi K. [4 ]
Winer, Eric P. [1 ]
Anders, Carey K. [2 ]
Zhao, Jean J. [1 ]
Lin, Nancy U. [1 ,5 ]
机构
[1] Dana Farber Canc Inst, Boston, MA USA
[2] Duke Canc Inst, Durham, NC USA
[3] Brigham & Womens Hosp, Boston, MA USA
[4] MD Anderson Canc Ctr, Houston, TX USA
[5] Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
关键词
INHIBITION;
D O I
10.1158/1078-0432.CCR-22-1138
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Brain metastases can occur in up to 50% of patients with metastatic HER2-positive breast cancer. Because patients with active brain metastases were excluded from previous pivotal clinical trials, the central nervous system (CNS) activity of the antibody-drug conjugate trastuzumab deruxtecan (T-DXd) is not well characterized. Experimental Design: We studied how T-DXd affects growth and overall survival in orthotopic patient-derived xenografts (PDX) of HER2-positive and HER2-low breast cancer brain metastases (BCBM). Separately, we evaluated the effects of T-DXd in a retrospective cohort study of 17 patients with stable or active brain metastases.Results: T-DXd inhibited tumor growth and prolonged survival in orthotopic PDX models of HER2-positive (IHC 3+) and HER2-low (IHC 2+/FISH ratio < 2) BCBMs. T-DXd reduced tumor size and prolonged survival in a T-DM1-resistant HER2-positive BCBM PDX model. In a retrospective multi-institutional cohort study of 17 patients with predominantly HER2-positive BCBMs, the CNS objec-tive response rate (ORR) was 73% (11/15) while extracranial response rate was 45% (5/11). In the subset of patients with untreated or progressive BCBM at baseline, the CNS ORR was 70% (7/10). The median time on treatment with T-DXd was 8.9 (1.3-16.2) months, with 42% (7/17) remaining on treatment at data cutoff. Conclusions: T-DXd demonstrates evidence of CNS activity in HER2-positive and HER2-low PDX models of BCBM and prelim-inary evidence of clinical efficacy in a multi-institution case series of patients with BCBM. Prospective clinical trials to further evaluate CNS activity of T-DXd in patients with active brain metastases are warranted.
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收藏
页码:174 / 182
页数:9
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