A review of the use of next generation sequencing methodologies to identify biomarkers of resistance to CDK4/6 inhibitors in ER+/HER2-breast cancer

被引:14
|
作者
Servetto, Alberto [1 ,2 ]
Napolitano, Fabiana [1 ]
Angelis, Carmine De [1 ,3 ]
Placido, Pietro De [1 ]
Giuliano, Mario [1 ]
Arpino, Grazia [1 ]
Placido, Sabino De [1 ]
Bianco, Roberto [1 ]
Formisano, Luigi [1 ]
机构
[1] Univ Naples Federico II, Dept Clin Med & Surg, Naples, Italy
[2] Univ Texas Southwestern Med Ctr Dallas, Simmons Comprehens Canc Ctr, Dallas, TX 75390 USA
[3] Baylor Coll Med, Lester & Sue Smith Breast Ctr, Houston, TX 77030 USA
关键词
CDK4/6; inhibitors; Next generation sequencing; Breast cancer; Precision medicine; CELL-CYCLE PROGRESSION; BREAST-CANCER; ACQUIRED-RESISTANCE; TUMOR-SUPPRESSOR; CDK6; INHIBITOR; FREE DNA; THERAPY; PALBOCICLIB; HETEROGENEITY; ABEMACICLIB;
D O I
10.1016/j.critrevonc.2020.103191
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The development of cyclin-dependent kinases (CDK) 4 and 6 inhibitors represented a substantial breakthrough in the treatment of estrogen receptor positive (ER+), human epidermal growth factor receptor 2 (HER2) negative metastatic breast cancer. These drugs showed a significant clinical benefit in pivotal clinical trials. However, resistance eventually occurs, leading to disease progression. Next Generation Sequencing methodologies have been employed to investigate predictive biomarkers of response or resistance to CDK4/6 inhibitors. Whole exome and targeted sequencing of solid and liquid biopsies have revealed several possible genomic alterations associated with resistance. Notably, genomic alterations identified by DNA-sequencing did not fully recapitulate the entire landscape of resistance to CDK4/6 inhibitors. Gene expression analysis, such as RNA-Seq methodologies, have provided insights into transcriptional profiles and may need further application. Herein, we report the main findings derived from the use of NGS analysis in the context of resistance to CDK4/6 inhibitors in ER + breast cancer.
引用
收藏
页数:10
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