aUniversity of Southern California bKeck School of Medicine cUSC/Norris Comprehensive Cancer and Department of Medicine, Los Angeles, California, USA.
Curr Opin Obstet Gynecol. 2014 Feb;26(1):27-33. doi: 10.1097/GCO.0000000000000043.
To review the most recent developments in the treatment of human epidermal growth factor receptor type 2 (HER2)-positive breast cancer with novel HER2-targeting agents and combinations that have significantly improved clinical outcomes.
Since the approval of trastuzumab 15 years ago, the natural history of HER2-positive breast cancer has been altered with improvements in survival for both early and advanced disease with the addition of this agent to standard chemotherapy. The HER2 receptor pathway drives breast cancer growth and aggressiveness, and HER2-targeted agents can improve survival in early and advanced disease. In the advanced setting, two new drugs have been approved since 2012, pertuzumab and ado-trastuzumab emtansine (T-DM1), both of which improve survival without any reciprocal increase in toxicity. However, resistance almost always ensues, pointing to the need to understand the driving mechanisms and to biomarkers that will help individualize therapy and point to newer signal transduction and other modulators.
HER2-positive breast cancer represents a distinct subtype with more aggressive clinical characteristics. HER2-targeted therapies, usually in combination with chemotherapy, are the standard of care, improving the cure rate in early-stage breast cancer and lengthening survival in the advanced setting.
回顾最近在使用新型人表皮生长因子受体 2(HER2)靶向药物和联合方案治疗 HER2 阳性乳腺癌方面的进展,这些药物显著改善了临床结局。
自 15 年前曲妥珠单抗获得批准以来,HER2 阳性乳腺癌的自然病程发生了改变,在标准化疗中加入该药物后,早期和晚期疾病的生存率均得到了提高。HER2 受体通路驱动乳腺癌的生长和侵袭性,HER2 靶向药物可改善早期和晚期疾病的生存。在晚期治疗中,自 2012 年以来已有两种新药获得批准,分别是帕妥珠单抗和曲妥珠单抗-美坦新偶联物(T-DM1),两者均能提高生存率,而毒性无相应增加。然而,几乎总是会出现耐药,这表明需要了解驱动机制以及生物标志物,以帮助实现个体化治疗,并指向新的信号转导和其他调节剂。
HER2 阳性乳腺癌是一种具有更具侵袭性临床特征的独特亚型。HER2 靶向治疗通常与化疗联合应用,是标准治疗方法,可提高早期乳腺癌的治愈率,并延长晚期疾病的生存时间。