How to Treat HR+/HER2-Metastatic Breast Cancer Patients after CDK4/6 Inhibitors: An Unfinished Story

被引:10
作者
Cogliati, Viola [1 ]
Capici, Serena [1 ]
Pepe, Francesca Fulvia [1 ]
di Mauro, Pierluigi [2 ]
Riva, Francesca [2 ]
Cicchiello, Federica [2 ]
Maggioni, Claudia [2 ]
Cordani, Nicoletta [3 ]
Cerrito, Maria Grazia [3 ]
Cazzaniga, Marina Elena [1 ,3 ]
机构
[1] ASST Monza, Phase Res Ctr 1, I-20900 Monza, MB, Italy
[2] ASST Monza, Oncol Unit, I-20900 Monza, MB, Italy
[3] Univ Milano Bicocca, Sch Med & Surg, I-20900 Monza, MB, Italy
来源
LIFE-BASEL | 2022年 / 12卷 / 03期
关键词
metastatic breast cancer; CDK4; 6; inhibitors; therapy resistance; treatment sequencing; KINASE; 4/6; INHIBITOR; ENDOCRINE THERAPY; PALBOCICLIB; RESISTANCE; FULVESTRANT; COMBINATION; MULTICENTER; ABEMACICLIB; STRATEGIES; RIBOCICLIB;
D O I
10.3390/life12030378
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
CDK4/6 inhibitors in association with endocrine therapy represent the best therapeutic choice for either endocrine-sensitive or resistant hormone-receptor-positive advanced breast cancer patients. On the contrary, the optimal therapeutic strategy after the failure of CDK4/6 inhibitors-based treatment still remains an open question worldwide. In this review, we analyze the most studied mechanisms of resistance to CDK4/6 inhibitors treatment, as well as the most significant results of retrospective and prospective trials in the setting of progression after CDK4/6 inhibitors, to provide the reader a comprehensive overview from both a preclinical and especially a clinical perspective. In our opinion, an approach based on a deeper knowledge of resistance mechanisms to CDK4/6 inhibitors, but also on a careful analysis of what is done in clinical practice, can lead to a better definition of prospective randomized trials, to implement a personalized sequence approach, based on molecular analyses.
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页数:17
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