The Dual PI3K/mTOR Pathway Inhibitor GDC-0084 Achieves Antitumor Activity in PIK3CA-Mutant Breast Cancer Brain Metastases

被引:59
作者
Ippen, Franziska M. [1 ,2 ]
Alvarez-Breckenridge, Christopher A. [3 ]
Kuter, Benjamin M. [1 ]
Fink, Alexandria L. [3 ]
Bihun, Ivanna, V [1 ]
Lastrapes, Matthew [4 ]
Penson, Tristan [3 ]
Schmidt, Stephen P. [5 ]
Wojtkiewicz, Gregory R. [6 ]
Ning, Jianfang [3 ]
Subramanian, Megha [1 ]
Giobbie-Hurder, Anita [7 ]
Martinez-Lage, Maria [8 ]
Carter, Scott L. [4 ]
Cahill, Daniel P. [3 ]
Wakimoto, Hiroaki [3 ]
Brastianos, Priscilla K. [1 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Canc Ctr, Boston, MA 02115 USA
[2] Heidelberg Univ Hosp, Dept Neurol, Heidelberg, Germany
[3] Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02115 USA
[4] Harvard Med Sch, Joint Ctr Canc Precis Med, Brigham & Womens Hosp, Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Harvard Med Sch, Ctr Syst Biol, Massachusetts Gen Hosp, Boston, MA 02115 USA
[6] Harvard Med Sch, Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02115 USA
[7] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[8] Harvard Med Sch, Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02115 USA
关键词
PI3K PATHWAY; EVEROLIMUS; RESISTANCE; MUTATIONS; EFFICACY; IMPACT; PIK3CA;
D O I
10.1158/1078-0432.CCR-18-3049
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Previous studies have shown that the PI3K/Akt/ mTORpathway is activated in up to 70% of breast cancer brain metastases, but there are no approved agents for affected patients. GDC-0084 is a brain penetrant, dual PI3K/mTOR inhibitor that has shown promising activity in a preclinical model of glioblastoma. The aim of this study was to analyze the efficacy of PI3K/mTOR blockade in breast cancer brain metastases models. Experimental Design: The efficacy of GDC-0084 was evaluated in PIK3CA-mutant and PIK3CA wild-type breast cancer cell lines and the isogenic pairs of PIK3CA wild-type and mutant (H1047R/thorn) MCF10A cells in vitro. In vitro studies included cell viability and apoptosis assays, cell-cycle analysis, and Western blots. In vivo, the effect of GDC-0084 was investigated in breast cancer brain metastasis xenograft mouse models and assessed by bioluminescent imaging and IHC. Results: In vitro, GDC-0084 considerably decreased cell viability, induced apoptosis, and inhibited phosphorylation of Akt and p70 S6 kinase in a dose-dependent manner in PIK3CA-mutant breast cancer brain metastatic cell lines. In contrast, GDC-0084 led only to growth inhibition in PIK3CA wild-type cell lines in vitro. In vivo, treatment with GDC-0084 markedly inhibited the growth of PIK3CA-mutant, with accompanying signaling changes, and not PIK3CA wild-type brain tumors. Conclusions: The results of this study suggest that the brainpenetrant PI3K/mTOR targeting GDC-0084 is a promising treatment option for breast cancer brain metastases with dysregulated PI3K/mTOR signaling pathway conferred by activating PIK3CA mutations. A national clinical trial is planned to further investigate the role of this compound in patients with brain metastases.
引用
收藏
页码:3374 / 3383
页数:10
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