A phase II study of oral enzastaurin in patients with metastatic breast cancer previously treated with an anthracycline and a taxane containing regimen

作者：Mina Lida; Krop Ian; Zon Robin T; Isakoff Steven J; Schneider Charles J; Yu Menggang; Johnson Cindy; Vaughn LaTrice G; Wang Yanping; Hristova Kazmierski Maria; Shonukan Oluwatoyin O; Sledge George W; Miller Kathy D^*

来源：Investigational New Drugs, 2009, 27(6): 565-570.

DOI：10.1007/s10637-009-9220-1

• Enzastaurin
• Metastatic breast cancer
• Phase II

Purpose: Enzastaurin is a potent, serine-threonine kinase inhibitor which selectively targets PKC beta and PI3K/AKT signaling pathways to reduce cell proliferation, induce apoptosis, and inhibit angiogenesis. As PKC beta and PI3K/AKT signaling are both involved in breast cancer pathogenesis, this phase II study evaluated the efficacy and toxicity of enzastaurin in previously treated patients with metastatic breast cancer (MBC). Patients and Methods: Eligible patients had histologically confirmed MBC with measurable disease, and must have received prior anthracycline and taxane chemotherapy, but not more than two prior regimens for MBC. Human epidermal growth factor 2 (HER2)-positive patients must have progressed on prior trastuzumab therapy. Enzastaurin, 1,125-mg loading dose on day 1 followed by 500 mg daily, was administered orally in 28-day cycles. Response was assessed every 2 cycles according to the Response Evaluation Criteria in Solid Tumors (RECIST) criteria. Results: Twenty-one patients enrolled between November 2006 and September 2007. Fourteen (66.7%) patients completed at least two cycles of therapy. No patients developed Grade 3/4 hematologic toxicity. Grade 3 nonhematologic toxicity was rare (< 5%) and most commonly attributed to MBC progression. There were no objective responses and no patients with stable disease for a parts per thousand yen6 months. Median progression-free survival was 1.68 months (95%CI: 1.02, 1.74). Conclusions: Enzastaurin monotherapy was well tolerated, but demonstrated no activity in patients with heavily pretreated MBC.

• 出版日期2009-12