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CDK4/6 inhibitors in HER2-positive breast cancer

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, sho...

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Bibliographic Details
Published in:Critical reviews in oncology/hematology 2017-04, Vol.112, p.208-214
Main Authors: Corona, Silvia Paola, Ravelli, Andrea, Cretella, Daniele, Cappelletti, Maria Rosa, Zanotti, Laura, Dester, Martina, Gobbi, Angela, Petronini, Pier Giorgio, Generali, Daniele
Format: Article
Language:English
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Summary: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.
ISSN:1040-8428
1879-0461
DOI:10.1016/j.critrevonc.2017.02.022