Activity of the dual kinase inhibitor lapatinib (GW572016) against HER-2-overexpressing and trastuzumab-treated breast cancer cells

GE Konecny, MD Pegram, N Venkatesan, R Finn… - Cancer research, 2006 - AACR
GE Konecny, MD Pegram, N Venkatesan, R Finn, G Yang, M Rahmeh, M Untch, DW Rusnak…
Cancer research, 2006AACR
Lapatinib (GW572016) is a selective inhibitor of both epidermal growth factor receptor
(EGFR) and HER-2 tyrosine kinases. Here, we explore the therapeutic potential of lapatinib
by testing its effect on tumor cell growth in a panel of 31 characterized human breast cancer
cell lines, including trastuzumab-conditioned HER-2-positive cell lines. We further
characterize its activity in combination with trastuzumab and analyze whether EGFR and
HER-2 expression or changes induced in the activation of EGFR, HER-2, Raf, AKT, or …
Abstract
Lapatinib (GW572016) is a selective inhibitor of both epidermal growth factor receptor (EGFR) and HER-2 tyrosine kinases. Here, we explore the therapeutic potential of lapatinib by testing its effect on tumor cell growth in a panel of 31 characterized human breast cancer cell lines, including trastuzumab-conditioned HER-2-positive cell lines. We further characterize its activity in combination with trastuzumab and analyze whether EGFR and HER-2 expression or changes induced in the activation of EGFR, HER-2, Raf, AKT, or extracellular signal-regulated kinase (ERK) are markers of drug activity. We report that concentration-dependent antiproliferative effects of lapatinib were seen in all breast cancer cell lines tested but varied significantly between individual cell lines with up to 1,000-fold difference in the IC50s (range, 0.010-18.6 μmol/L). Response to lapatinib was significantly correlated with HER-2 expression and its ability to inhibit HER-2, Raf, AKT, and ERK phosphorylation. Long-term in vivo lapatinib studies were conducted with human breast cancer xenografts in athymic mice. Treatment over 77 days resulted in a sustained and significant reduction in xenograft volume compared with untreated controls. For the combination of lapatinib plus trastuzumab, synergistic drug interactions were observed in four different HER-2-overexpressing cell lines. Moreover, lapatinib retained significant in vitro activity against cell lines selected for long-term outgrowth (>9 months) in trastuzumab-containing (100 μg/mL) culture medium. These observations provide a clear biological rationale to test lapatinib as a single agent or in combination with trastuzumab in HER-2-overexpressing breast cancer and in patients with clinical resistance to trastuzumab. (Cancer Res 2006; 66(3): 1630-9)
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