The role of CDK4/6 inhibitors in early breast cancer

被引:14
|
作者
Gil-Gil, Miguel [1 ]
Alba, Emilio [2 ]
Gavila, Joaquin [3 ]
de la Haba-Rodriguez, Juan [4 ]
Ciruelos, Eva [5 ]
Tolosa, Pablo [5 ]
Candini, Daniele [6 ]
Llombart-Cussac, Antonio [7 ,8 ]
机构
[1] Inst Catala Oncol IDIBELL, Barcelona, Spain
[2] Hosp Clin Univ Virgen Victoria, Dept Med Oncol, Malaga, Spain
[3] Fdn Inst Valenciano Oncol, Valencia, Spain
[4] Hosp Univ Reina Sofia, Inst Invest Biomed Cordoba IMIBIC, Dept Med Oncol, Cordoba, Spain
[5] Univ Hosp 12 Octubre, Dept Med Oncol, Madrid, Spain
[6] Pfizer Oncol, Med Dept, Madrid, Spain
[7] Hosp Arnau Vilanova, Dept Med Oncol, Calle St Clement 12, Valencia 46015, Spain
[8] Univ Catolica Valencia, FISABIO, Valencia, Spain
关键词
Early breast cancer; Cyclin-dependent kinase 4/6 inhibitors; Adjuvant therapy; Palbociclib; Abemaciclib; RIBOCICLIB PLUS LETROZOLE; KINASE; 4/6; INHIBITOR; ENDOCRINE THERAPY; POSTMENOPAUSAL WOMEN; OPEN-LABEL; PALBOCICLIB; RESISTANCE; MULTICENTER; CHEMOTHERAPY; ABEMACICLIB;
D O I
10.1016/j.breast.2021.05.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The use of cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) has proven to be a successful strategy in the treatment of advanced hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2(-)) breast cancer (BC), leading to a strong interest in their possible role in the treatment of early luminal BC. In this review we collect the most relevant and recent information on the use of CDK4/6i for the treatment of early BC in the neoadjuvant and adjuvant settings. Specifically, we evaluate the results of the large phase 3 adjuvant trials recently released, which have yielded apparently divergent results. We also examine the relevance of biomarkers as response predictive factors for CDI4/6i, the combination between radiotherapy and CDK4/6i, and provide a critical discussion on the evidence that we have so far and future directions of the role of these drugs in the treatment of early BC. (C) 2021 Published by Elsevier Ltd.
引用
收藏
页码:160 / 169
页数:10
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