Institute for Cancer Research, Unit of Investigative Clinical Oncology (INCO), Candiolo, Italy.
Expert Opin Pharmacother. 2012 Oct;13(15):2143-56. doi: 10.1517/14656566.2012.725723.
Endocrine therapy is a fundamental component of the therapeutic repertoire for treatment of metastatic, hormone receptor-positive breast cancer. Inevitably, however, tumors develop resistance to these compounds, and overcoming this phenomenon is a key motivator of research in this field.
This review summarizes the current status of endocrine therapy for the treatment of metastatic disease, with a main focus on postmenopausal patients. Furthermore, strategies that could potentially sustain endocrine resistance and future perspectives in this direction are also to be described. Relevant references were identified by PubMed searches and from the abstract books of the annual meetings of The European Society of Clinical Oncology (ESMO), The American Society of Clinical Oncology (ASCO) and from the San Antonio Breast Cancer Symposia.
Combinations of endocrine therapy with HER2 targeting agents, as well as with compounds that can interfere with PI3K/Akt/mTOR signaling, are two promising strategies for delaying or overcoming endocrine resistance, mediated by these relevant biological pathways. Due to increased costs and the burden of toxicity associated with these combination therapies, compared to endocrine therapy alone, it is imperative to concentrate efforts on establishing biomarkers that can predict efficacy.
内分泌治疗是治疗转移性、激素受体阳性乳腺癌的治疗方案中的基本组成部分。然而,肿瘤不可避免地会对这些化合物产生耐药性,克服这种现象是该领域研究的主要动力。
本文综述了内分泌治疗转移性疾病的现状,主要关注绝经后患者。此外,还描述了可能维持内分泌耐药的策略以及该领域的未来展望。相关参考文献通过 PubMed 搜索和欧洲临床肿瘤学会(ESMO)、美国临床肿瘤学会(ASCO)年会的摘要集以及圣安东尼奥乳腺癌研讨会确定。
内分泌治疗联合 HER2 靶向药物以及能干扰 PI3K/Akt/mTOR 信号通路的化合物是两种有前途的策略,可以延迟或克服这些相关生物学途径介导的内分泌耐药。由于与内分泌治疗相比,这些联合治疗的成本增加和毒性负担增加,因此必须集中精力建立能够预测疗效的生物标志物。