Department of Medical Oncology and Therapeutics Research, City of Hope Cancer Center, Duarte, California, USA.
Oncologist. 2011;16(6):760-71. doi: 10.1634/theoncologist.2010-0345. Epub 2011 May 4.
Newer treatments have improved survival for patients with metastatic breast cancer over the last two decades, and a battery of new cytotoxic and targeted therapies is continuing to enhance this trend. This review outlines recent data and ongoing research in this area, by highlighting new developments (regarding approved but relatively new classes of cytotoxic and targeted agents) and also new classes of targeted therapy that are undergoing clinical evaluation. Mechanisms for synergy between agents are discussed where data are available, as is information on the rationale behind the development of agents that inhibit angiogenesis, DNA repair, histone deacetylases, heat shock proteins, or various signaling pathways in tumor proliferation. The abundance of clinical research surrounding anticancer agents, together with ongoing cancer biology research, is expected to further increase the available pool of therapeutic options for metastatic breast cancer. Concomitantly, in the absence of an effective targeted monotherapy, a better understanding of the interplay between biologic and cytotoxic anticancer agents will improve our ability to rationally design combination regimens with better efficacy and tolerability.
在过去的二十年中,新型治疗方法已经改善了转移性乳腺癌患者的生存情况,并且一系列新的细胞毒性和靶向治疗方法也在继续增强这一趋势。本文通过突出新的发展(关于已批准但相对较新的细胞毒性和靶向药物类别)以及正在进行临床评估的新类别的靶向治疗,概述了这一领域的最新数据和正在进行的研究。只要有数据,就会讨论药物之间协同作用的机制,以及抑制血管生成、DNA 修复、组蛋白去乙酰化酶、热休克蛋白或肿瘤增殖中各种信号通路的药物开发背后的原理信息。围绕抗癌药物的大量临床研究,以及癌症生物学研究的不断进展,预计将进一步增加转移性乳腺癌的治疗选择。同时,在缺乏有效靶向单药治疗的情况下,更好地了解生物和细胞毒性抗癌药物之间的相互作用将提高我们合理设计具有更好疗效和耐受性的联合方案的能力。