Unknown

Dataset Information

0

Current Therapeutic Progress of CDK4/6 Inhibitors in Breast Cancer.


ABSTRACT: The clinical use of selective cyclin-dependent kinase (CDK) 4/6 inhibitors has significantly improved the prognosis of patients with hormone receptor (HR)-positive human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer (ABC/mBC), which almost achieved the double progression-free survival (PFS) in combination with endocrine therapy (ET) compared with ET alone. To date, there are 3 CDK4/6 inhibitors (palbociclib, ribocilcib and abemaciclib) approved by the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) to treat patients with HR+/HER2-ABC/mBC in the first and later lines. The aim of this review is to summarize the current clinical use and ongoing clinical trials of CDK4/6 inhibitors, the published overall survival data, and the potential biomarkers and resistance to CDK4/6 inhibitors.

SUBMITTER: Wu Y 

PROVIDER: S-EPMC7237121 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

altmetric image

Publications

Current Therapeutic Progress of CDK4/6 Inhibitors in Breast Cancer.

Wu Yanmei Y   Zhang Yu Y   Pi Hao H   Sheng Yuan Y  

Cancer management and research 20200515


The clinical use of selective cyclin-dependent kinase (CDK) 4/6 inhibitors has significantly improved the prognosis of patients with hormone receptor (HR)-positive human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer (ABC/mBC), which almost achieved the double progression-free survival (PFS) in combination with endocrine therapy (ET) compared with ET alone. To date, there are 3 CDK4/6 inhibitors (palbociclib, ribocilcib and abemaciclib) approved by the US  ...[more]

Similar Datasets

| S-EPMC2819039 | biostudies-other
| S-EPMC6533626 | biostudies-literature
| S-EPMC8706744 | biostudies-literature
| S-EPMC7563142 | biostudies-literature
| S-EPMC7118338 | biostudies-literature
| S-EPMC10745860 | biostudies-literature
2024-10-10 | GSE279160 | GEO
| S-EPMC8327758 | biostudies-literature
| S-EPMC4794996 | biostudies-literature
| S-EPMC7554788 | biostudies-literature