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三阴性乳腺癌的临床试验

Clinical trials in triple negative breast cancer.

作者信息

Reeder-Hayes Katherine E, Carey Lisa A, Sikov William M

机构信息

Department of Hematology-Oncology, University of North Carolina at Chapel Hill, UNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina, USA.

出版信息

Breast Dis. 2010;32(1-2):123-36. doi: 10.3233/BD-2010-0310.

Abstract

Triple negative breast cancer (TNBC) is an aggressive subtype of the disease against which targeted therapies that significantly improve the prognosis for hormone receptor-positive and HER2-overexpressing breast cancers are ineffective. This article summarizes our current understanding of the biology of TNBC as it relates to the efficacy of standard and investigational therapies. It reviews promising preliminary results that have been achieved with chemotherapeutic agents including the platinum analogs and agents that inhibit DNA repair by targeting poly ADP-ribose polymerase (PARP), while anti-angiogenic therapies and those that target the epidermal growth factor receptor (EGFR) have had more limited success. Agents that target a number of other pathways which appear to influence the biologic aggressiveness of TNBC, including src and PI3K, are in early stage clinical trials. As we learn more about TNBC, and which of its characteristics determine treatment response and resistance, we should become better able to select appropriate therapies for biologically defined patient subgroups, and reduce the clinical burden of this disease.

摘要

三阴性乳腺癌(TNBC)是一种侵袭性疾病亚型,针对激素受体阳性和HER2过表达乳腺癌能显著改善预后的靶向治疗对其无效。本文总结了我们目前对TNBC生物学特性的理解,以及这些特性与标准治疗和试验性治疗疗效的关系。文中回顾了使用化疗药物(包括铂类类似物和通过靶向聚ADP-核糖聚合酶(PARP)抑制DNA修复的药物)所取得的有前景的初步结果,而抗血管生成疗法和靶向表皮生长因子受体(EGFR)的疗法取得的成功较为有限。针对一些似乎影响TNBC生物学侵袭性的其他途径(包括src和PI3K)的药物正处于早期临床试验阶段。随着我们对TNBC了解得更多,以及其哪些特征决定治疗反应和耐药性,我们应该能够更好地为生物学定义的患者亚组选择合适的治疗方法,并减轻这种疾病的临床负担。

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