Montagna Emilia, Colleoni Marco
Division of Medical Senology, European Institute of Oncology, Via Ripamonti 435, Milan, 20141, Italy.
Division of Medical Senology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Ther Adv Med Oncol. 2019 Dec 16;11:1758835919894105. doi: 10.1177/1758835919894105. eCollection 2019.
Approximately 50% of HER2 positive breast cancer cases are also estrogen receptor (ER) positive. Data supports a role for close cross-talk between the ER and HER2 signaling pathways as an important contributor to the development of or acquired resistance to hormone therapies. Therefore a strategy that simultaneously blocks both signaling pathways is a reasonable approach to prevent or overcome either endocrine or anti-HER2 therapy resistance. Moreover, preclinical data support the idea that PI3K inhibitors and CDK4/6 could be an attractive target that functions downstream of both ER and HER2 pathways. We conducted a literature review of the results of phase II and III studies testing targeted therapies in metastatic breast cancer with HER2-positive and hormonal-receptor-positive disease. The analyses included efficacy and toxicity data from earlier studies with a single anti-HER2 drug combined with hormonal therapy up to more recent studies testing new molecules targeting these signaling pathways. The aims of this review are to summarize current knowledge and to discuss research development including the possibility to spare chemotherapy in this subgroup of HER2-positive breast cancer patients.
大约50%的HER2阳性乳腺癌病例同时也是雌激素受体(ER)阳性。数据支持ER和HER2信号通路之间密切的相互作用在激素疗法耐药性的产生或获得中起重要作用。因此,同时阻断这两条信号通路的策略是预防或克服内分泌或抗HER2治疗耐药性的合理方法。此外,临床前数据支持PI3K抑制剂和CDK4/6可能是一个有吸引力的靶点,其作用于ER和HER2通路的下游。我们对II期和III期研究结果进行了文献综述,这些研究测试了针对HER2阳性和激素受体阳性转移性乳腺癌的靶向治疗。分析包括早期单一抗HER2药物联合激素治疗的研究以及最近测试靶向这些信号通路新分子的研究的疗效和毒性数据。本综述的目的是总结当前知识,并讨论研究进展,包括在这一HER2阳性乳腺癌患者亚组中避免化疗的可能性。