Lester and Sue Smith Breast Center and the Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas, 77030; email:
Annu Rev Med. 2015;66:111-28. doi: 10.1146/annurev-med-042513-015127.
HER2 (ErbB2), a member of the HER family of tyrosine kinase receptors (HER1-4), is a major driver of tumor growth in 20% of breast cancers. Treatment with the anti-HER2 monoclonal antibody trastuzumab has revolutionized the outcome of patients with this aggressive breast cancer subtype, but intrinsic and acquired resistance is common. Growing understanding of the biology and complexity of the HER2 signaling network and of potential resistance mechanisms has guided the development of new HER2-targeted agents. Combinations of these drugs to more completely inhibit the HER receptor layer, or combining HER2-targeted agents with agents that target downstream signaling, alternative pathways, or components of the host immune system, are being vigorously investigated in the preclinical and clinical settings. As a result, the list of more effective and well tolerated FDA-approved new regimens for patients with HER2+ tumors is constantly growing.
人表皮生长因子受体 2(HER2),又称 ErbB2,是表皮生长因子受体家族(HER1-4)的一员,是 20%乳腺癌肿瘤生长的主要驱动因素。抗 HER2 单克隆抗体曲妥珠单抗的应用彻底改变了这种侵袭性乳腺癌亚型患者的预后,但该药物存在原发性和获得性耐药。人们对 HER2 信号网络的生物学和复杂性以及潜在耐药机制的认识不断加深,这指导了新型 HER2 靶向药物的开发。这些药物的联合应用旨在更完全地抑制 HER 受体层,或联合使用 HER2 靶向药物与靶向下游信号、替代途径或宿主免疫系统成分的药物,目前正在临床前和临床研究中进行广泛研究。因此,针对 HER2+肿瘤患者的更有效且耐受更好的新型 FDA 批准方案不断增加。