Ocaña Alberto, Amir Eitan
Drug Development Program, Princess Margaret Hospital, Toronto, Canada M5G 2M9.
Cancer Treat Rev. 2009 Dec;35(8):685-91. doi: 10.1016/j.ctrv.2009.08.001. Epub 2009 Sep 4.
Aberrant activation of HER2 through overexpression has been shown to play an important role in some breast cancers. Therapies against this receptor including the monoclonal antibody, trastuzumab, or the small tyrosine kinase inhibitor, lapatinib have shown to improve the prognosis of such patients. Despite overexpressing HER2, some patients do not respond to these targeted treatments or progress after a short period of time. Irreversible tyrosine kinase inhibitors have been developed to bypass several pathways that could be involved in this resistance. In vitro, these agents have been shown to be more potent and to prolong target inhibition. Clinical development of these agents is ongoing and early results are promising. This review will describe the biologic rationale that justifies the development of these agents in breast cancer focusing on the current status and future directions.
HER2通过过表达而发生的异常激活已被证明在某些乳腺癌中起重要作用。针对该受体的疗法,包括单克隆抗体曲妥珠单抗或小分子酪氨酸激酶抑制剂拉帕替尼,已显示可改善此类患者的预后。尽管HER2过表达,但一些患者对这些靶向治疗无反应或在短时间后病情进展。已开发出不可逆酪氨酸激酶抑制剂以绕过可能参与这种耐药性的几种途径。在体外,这些药物已显示出更强效并能延长靶点抑制时间。这些药物的临床开发正在进行中,早期结果很有前景。本综述将描述在乳腺癌中开发这些药物的生物学原理,重点关注当前状况和未来方向。