Hamilton Erika P, Jeselsohn Rinath M, Vahdat Linda T, Hurvitz Sara A
Breast Cancer Research Program, Sarah Cannon Research Institute, 335 24th Avenue North, Suite 300, Nashville, TN, 37203, USA.
Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Target Oncol. 2025 May;20(3):431-444. doi: 10.1007/s11523-025-01137-5. Epub 2025 May 6.
The estrogen receptor (ER) signaling pathway is a key driver of breast cancer, primarily through the activation of genes that promote tumor cell survival and growth. The recommended first-line treatment for ER-positive (ER+)/human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer is endocrine therapy plus a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor. However, most patients experience disease progression, and there is no clear standard of care in the second-line setting. Thus, novel treatments in the advanced setting are needed. In this narrative review, we describe the unique mechanisms of action of a new class of drugs called PROteolysis TArgeting Chimera (PROTAC) ER degraders. Unlike other ER-targeted therapies, these small molecules harness the body's primary intracellular natural protein disposal machinery, the ubiquitin-proteasome system, to directly induce ER degradation. Vepdegestrant (ARV-471) is the furthest advanced PROTAC ER degrader currently in clinical development. Preclinical data demonstrate increased tumor growth inhibition with vepdegestrant alone or in combination with CDK4/6 inhibitors compared with the selective ER degrader fulvestrant. In a first-in-human phase 1/2 clinical study, vepdegestrant administered orally as monotherapy or in combination with palbociclib showed promising clinical activity and a favorable safety profile in patients with heavily pretreated ER+/HER2- advanced breast cancer. Several other PROTAC ER degraders (AC699, ERD-3111, ERD-4001, and HP568) are in early development and have demonstrated activity in preclinical breast cancer models, with some recently entering clinical trials. The data highlight the potential for PROTAC ER degraders to be a new backbone therapy in breast cancer.
雌激素受体(ER)信号通路是乳腺癌的关键驱动因素,主要通过激活促进肿瘤细胞存活和生长的基因来实现。对于雌激素受体阳性(ER+)/人表皮生长因子受体2阴性(HER2-)的晚期或转移性乳腺癌,推荐的一线治疗方案是内分泌治疗联合细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂。然而,大多数患者会出现疾病进展,并且二线治疗中尚无明确的标准治疗方案。因此,需要针对晚期乳腺癌的新型治疗方法。在这篇叙述性综述中,我们描述了一类名为蛋白酶靶向嵌合体(PROTAC)的新型ER降解剂的独特作用机制。与其他靶向ER的疗法不同,这些小分子利用人体主要的细胞内天然蛋白质处理机制——泛素-蛋白酶体系统,直接诱导ER降解。维泊妥珠单抗(ARV-471)是目前临床开发中进展最靠前的PROTAC ER降解剂。临床前数据表明,与选择性ER降解剂氟维司群相比,单独使用维泊妥珠单抗或与CDK4/6抑制剂联合使用时,肿瘤生长抑制作用增强。在一项首次人体1/2期临床研究中,维泊妥珠单抗单药口服或与哌柏西利联合使用,在预处理严重的ER+/HER2-晚期乳腺癌患者中显示出有前景的临床活性和良好的安全性。其他几种PROTAC ER降解剂(AC699、ERD-3111、ERD-4001和HP568)正处于早期开发阶段,并已在临床前乳腺癌模型中显示出活性,其中一些最近已进入临床试验。这些数据凸显了PROTAC ER降解剂成为乳腺癌新的基础治疗方法的潜力。