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CDK4/6 inhibitors in HER2-positive breast cancer.
- Source :
-
Critical reviews in oncology/hematology [Crit Rev Oncol Hematol] 2017 Apr; Vol. 112, pp. 208-214. Date of Electronic Publication: 2017 Feb 24. - Publication Year :
- 2017
-
Abstract
- Notwithstanding the continuous progress made in cancer treatment in the last 20 years, and the availability of new targeted therapies, metastatic Breast Cancer (BC) is still incurable. Targeting the cell cycle machinery has emerged as an attractive strategy to tackle cancer progression, showing very promising results in the preclinical and clinical settings. The first selective inhibitors of CDK4/6 received breakthrough status and FDA approval in combination with letrozole (February 2015) and fulvestrant (February 2016) as first-line therapy in ER-positive advanced and metastatic BC. Considering the success of this family of compounds in hormone-positive BC, new possible applications are being investigated in other molecular subtypes. This review summarizes the latest findings on the use of CDK4/6 inhibitors in HER2 positive BC.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Subjects :
- Cyclin-Dependent Kinase 4 antagonists & inhibitors
Cyclin-Dependent Kinase 6 antagonists & inhibitors
Estradiol analogs & derivatives
Estradiol therapeutic use
Fulvestrant
Humans
Letrozole
Nitriles therapeutic use
Protein Kinase Inhibitors therapeutic use
Receptor, ErbB-2 biosynthesis
Triazoles therapeutic use
Breast Neoplasms drug therapy
Molecular Targeted Therapy methods
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0461
- Volume :
- 112
- Database :
- MEDLINE
- Journal :
- Critical reviews in oncology/hematology
- Publication Type :
- Academic Journal
- Accession number :
- 28325261
- Full Text :
- https://doi.org/10.1016/j.critrevonc.2017.02.022