Biomarkers Unit, Department of applied research and technological development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Clinical Research Methodology Laboratory, IRCCS Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.
Breast. 2021 Feb;55:75-78. doi: 10.1016/j.breast.2020.12.006. Epub 2020 Dec 13.
Cell-cycle abnormalities are common in estrogen receptor- and/or progesterone receptor-positive, and HER2-non-overexpressing (HR+/HER2-) breast cancer, and have long been considered potential therapeutic targets. Cyclin-dependent kinase (CDK) 4/6 inhibitors have dramatically changed the therapeutic management of HR+/HER2-advanced breast cancer by prolonging progression-free and overall survival when given in combination with endocrine therapy. In this article, available data from PALLAS and monarchE trials regarding the efficacy and toxicity of adjuvant combined therapy with CDK 4/6 inhibitors and endocine therapy in HR+/HER2-early breast cancer are reviewed, and relevant issues including study hypothesis, patient selection, and duration of follow-up are discussed.
细胞周期异常在雌激素受体(ER)和/或孕激素受体(PR)阳性、HER2 无过表达(HR+/HER2-)的乳腺癌中很常见,长期以来一直被认为是潜在的治疗靶点。细胞周期蛋白依赖性激酶(CDK)4/6 抑制剂与内分泌治疗联合应用时,可显著延长无进展生存期和总生存期,从而改变了 HR+/HER2-晚期乳腺癌的治疗管理。本文回顾了 PALLAS 和 monarchE 试验中关于 CDK4/6 抑制剂联合内分泌治疗辅助治疗 HR+/HER2-早期乳腺癌的疗效和毒性的可用数据,并讨论了相关问题,包括研究假设、患者选择和随访时间。