Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois.
JAMA Oncol. 2015 Jul;1(4):528-34; quiz 549. doi: 10.1001/jamaoncol.2015.1198.
Advances in understanding tumor biology, particularly signaling pathways, have led to the development and approval of many novel agents and have changed the landscape of therapy for patients with metastatic breast cancer. This review highlights some of the recent successes and failures in breast cancer drug development, including strategies to overcome endocrine and human epidermal growth factor 2-neu (HER2) resistance, targeting triple-negative breast cancers (which do not express the HER2, estrogen, and progesterone receptors) through novel receptors, harnessing the immune system, and new ways of targeting angiogenesis. For patients with metastatic breast cancer, expanding therapeutic options through clinical trial participation is a crucial part of modern oncology practice. As we continue to learn how to use targeted therapies in the context of genomic medicine, analysis of the tumor in real-time may become increasingly important, giving researchers the information needed to start combining therapies in a biologically informed manner.
肿瘤生物学的进展,尤其是信号通路的研究,推动了许多新型药物的开发和审批,并改变了转移性乳腺癌患者的治疗格局。本综述重点介绍了乳腺癌药物研发的一些近期成功和失败案例,包括克服内分泌和人表皮生长因子 2 受体(HER2)耐药的策略,通过新型受体靶向三阴性乳腺癌(既不表达 HER2、雌激素和孕激素受体),利用免疫系统,以及血管生成的新靶点。对于转移性乳腺癌患者,通过临床试验参与来扩大治疗选择是现代肿瘤学实践的关键部分。随着我们继续学习如何在基因组医学的背景下使用靶向治疗,实时分析肿瘤可能变得越来越重要,为研究人员提供了以生物信息方式组合治疗所需的信息。