Cetin Bulent, Wabl Chiara A, Gumusay Ozge
Department of Internal Medicine, Division of Medical Oncology, Suleyman Demirel University Faculty of Medicine, Isparta, 32260, Turkey.
University of California, San Francisco School of Medicine, San Francisco, CA 94143, USA.
Future Oncol. 2022 Mar;18(9):1143-1157. doi: 10.2217/fon-2021-0842. Epub 2022 Feb 9.
Hormone receptor (HR)-positive, HER2-negative tumors represent the most common form of metastatic breast cancer (MBC), and endocrine therapy has been the mainstay treatment for several decades. Recently, a novel drug class called CDK4/6 inhibitors in combination with endocrine therapy have remarkably improved the outcome of patients with HR-positive, HER2-negative MBC by targeting the cell cycle machinery and overcoming aspects of endocrine resistance. Several potential cell-cycle-specific and nonspecific mechanisms of resistance to CDK4/6 inhibitors have been reported in recent studies. This review discusses potential resistance mechanisms to CDK4/6 inhibitors, the use of biomarkers to guide treatment for HR-positive, HER2-negative MBC and possible approaches to overcome resistance to CDK4/6 inhibitors.
激素受体(HR)阳性、人表皮生长因子受体2(HER2)阴性肿瘤是转移性乳腺癌(MBC)最常见的形式,几十年来内分泌治疗一直是主要治疗方法。最近,一类名为细胞周期蛋白依赖性激酶4/6(CDK4/6)抑制剂的新型药物与内分泌治疗联合使用,通过靶向细胞周期机制并克服内分泌耐药的某些方面,显著改善了HR阳性、HER2阴性MBC患者的治疗结果。最近的研究报道了几种对CDK4/6抑制剂潜在的细胞周期特异性和非特异性耐药机制。本文综述讨论了对CDK4/6抑制剂的潜在耐药机制、使用生物标志物指导HR阳性、HER2阴性MBC的治疗以及克服对CDK4/6抑制剂耐药的可能方法。