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 |
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container_end_page | 1994 |
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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 |
format | Article |
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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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