An ERBB1-3 Neutralizing Antibody Mixture With High Activity Against Drug-Resistant HER2+Breast Cancers With ERBB Ligand Overexpression

作者：Schwarz Luis J; Hutchinson Katherine E; Rexer Brent N; Estrada Monica Valeria; Ericsson Paula I Gonzalez; Sanders Melinda E; Dugger Teresa C; Formisano Luigi; Guerrero Zotano Angel; Red Brewer Monica; Young Christian D; Lantto Johan; Pedersen Mikkel W; Kragh Michael; Horak Ivan D; Arteaga Carlos L^*

来源：JNCI-Journal of the National Cancer Institute, 2017, 109(11): djx065.

DOI：10.1093/jnci/djx065

Background: Plasticity of the ERBB receptor network has been suggested to cause acquired resistance to anti-human epidermal growth factor receptor 2 (HER2) therapies. Thus, we studied whether a novel approach using an ERBB1-3-neutralizing antibody mixture can block these compensatory mechanisms of resistance.
Methods: HER2 t cell lines and xenografts (n >= 6 mice per group) were treated with the ERBB1-3 antibody mixture Pan-HER, trastuzumab/lapatinib (TL), trastuzumab/pertuzumab (TP), or T-DM1. Downregulation of ERBB receptors was assessed by immunoblot analysis and immunohistochemistry. Paired pre- and post-T-DM1 tumor biopsies from patients (n = 11) with HER2-amplified breast cancer were evaluated for HER2 and P-HER3 expression by immunohistochemistry and/or fluorescence in situ hybridization. ERBB ligands were measured by quantitative reverse transcription polymerase chain reaction. Drug resistant cells were generated by chronic treatment with T-DM1. All statistical tests were two-sided.
Results: Treatment with Pan-HER inhibited growth and promoted degradation of ERBB1-3 receptors in a panel of HER2+ breast cancer cells. Compared with TL, TP, and T-DM1, Pan-HER induced a similar antitumor effect against established BT474 and HCC1954 tumors, but was superior to TL against MDA-361 xenografts (TL mean = 2026 mm(3), SD = 924 mm(3), vs Pan-HER mean = 565 mm(3), SD = 499 mm(3), P = .04). Pan-HER-treated BT474 xenografts did not recur after treatment discontinuation, whereas tumors treated with TL, TP, and T-DM1 did Post-TP and post-T-DM1 recurrent tumors expressed higher levels of neuregulin-1 (NRG1), HER3 and P-HER3 (all P <.05). Higher levels of P-HER3 protein and NRG1 mRNA were also observed in HER2 I breast cancers progressing after T-DM1 and trastuzumab (NRG1 transcript fold change +/- SD; pretreatment = 2, SD = 1.9, vs post-treatment = 11.4, SD = 10.3, P =.04). The HER3-neutralizing antibody LJM716 resensitized the drug-resistant cells to T-DM1, suggesting a causal association between the NRG1HER3 axis and drug resistance. Finally, Pan-HER treatment inhibited growth of HR6 trastuzumab- and T-DM1-resistant xenografts.
Conclusions: These data suggest that upregulation of a NRG1-HER3 axis can mediate escape from anti-HER2 therapies. Further, multitargeted antibody mixtures, such as Pan-HER, can simultaneously remove and/or block targeted ERBB receptor and ligands, thus representing an effective approach against drug sensitive and-resistant HER2+ cancers.

• 出版日期2017-11