Cyclin-dependent kinase 4/6 inhibitors in hormone receptor-positive early breast cancer: preliminary results and ongoing studies

被引:14
作者
Kwapisz, Dorota [1 ]
机构
[1] Specialist Outpatient Clin, Warsaw, Poland
关键词
CDK4; 6; inhibitors; Early breast cancer; Palbociclib; Ribociclib; Abemaciclib; CELL PROLIFERATION; DOUBLE-BLIND; PALBOCICLIB; LETROZOLE; FULVESTRANT; COMBINATION; RIBOCICLIB; THERAPY; PROTEIN; PLACEBO;
D O I
10.1007/s12282-018-0864-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cyclin D-cyclin-dependent kinase (CDK) 4/6-inhibitors (CDK4/6i) induce cell cycle arrest in the G1 phase what eventually can prevent the proliferation of cancer cells. The CDK4/6i have changed the landscape of treatment options for ER-positive, HER2-negative metastatic breast cancer. Currently, palbociclib, ribociclib, and abemaciclib are approved by the US Food and Drug Administration in this setting. This success encouraged the researchers to examine CDK4/6i activity in (neo)adjuvant setting. In this review, clinical data to date and ongoing clinical trials with palbociclib, ribociclib, and abemaciclib in the early breast cancer are discussed. A literature search of these topics was carried out using PubMed and data reported at international oncology meetings and clinicaltrials.gov were included. Currently, we have the early promising data from Phase II clinical trials of CDK4/6i efficacy in the neoadjuvant setting in women with HR-positive breast cancer. Moreover, there are numerous studies that are in progress today in (neo)adjuvant setting.
引用
收藏
页码:506 / 516
页数:11
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