CDK4 and CDK6 Inhibition in Breast Cancer — A New Standard

Breast cancer is the most prevalent type of malignant neoplasm worldwide, and estrogen-receptor (ER)–positive breast cancer is the most common phenotype. Outcomes continue to improve, but many patients present with advanced disease or have recurrence of disease that progressively becomes resistant t...

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Veröffentlicht in:The New England journal of medicine 2016-11, Vol.375 (20), p.1993-1994
1. Verfasser: Wolff, Antonio C
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container_end_page 1994
container_issue 20
container_start_page 1993
container_title The New England journal of medicine
container_volume 375
creator Wolff, Antonio C
description Breast cancer is the most prevalent type of malignant neoplasm worldwide, and estrogen-receptor (ER)–positive breast cancer is the most common phenotype. Outcomes continue to improve, but many patients present with advanced disease or have recurrence of disease that progressively becomes resistant to endocrine therapy. Efforts to enhance responsiveness to treatment and to overcome primary or acquired resistance through cotargeting of estrogen and cell proliferation–survival signaling pathways led to the recent approval of phosphatidylinositol 3-kinase–Akt–mammalian target of rapamycin (PI3K/Akt/mTOR) and cyclin-dependent kinase 4 and 6 (CDK4 and CDK6) inhibitors for the treatment of advanced ER-positive, human epidermal growth factor receptor 2 . . .
doi_str_mv 10.1056/NEJMe1611926
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subjects 1-Phosphatidylinositol 3-kinase
AKT protein
Breast cancer
Breast Neoplasms
Cancer therapies
Cell proliferation
Cell survival
Cyclin-dependent kinase 4
Cyclin-Dependent Kinase 6
Cyclin-dependent kinases
Endocrine therapy
Epidermal growth factor
Estrogen receptors
Humans
Inhibitor drugs
Neoplasia
Phenotypes
Proto-Oncogene Proteins
Rapamycin
TOR protein
title CDK4 and CDK6 Inhibition in Breast Cancer — A New Standard
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