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Does CDKN2A Loss Predict Palbociclib Benefit?
Author(s) -
Jennifer J. Gao,
R.P. Adams,
Sandra M. Swain
Publication year - 2015
Publication title -
current oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 51
eISSN - 1718-7729
pISSN - 1198-0052
DOI - 10.3747/co.22.2700
Subject(s) - palbociclib , cdkn2a , medicine , letrozole , kinase , breast cancer , estrogen receptor , oncology , cancer research , cyclin dependent kinase , regulator , cancer , pharmacology , metastatic breast cancer , cell cycle , biology , tamoxifen , microbiology and biotechnology , biochemistry , gene
Palbociclib, an oral small-molecule inhibitor of cyclin-dependent kinases 4 and 6, was recently approved by the U.S. Food and Drug Administration in combination with letrozole for postmenopausal women with advanced hormone receptor-positive, her2-negative breast cancer. Patients with loss of CDKN2A (p16), an inherent negative regulator of cyclin-dependent kinases 4 and 6, were not separately studied because of the significant response of the patients selected based only on receptor status. Here, we report a patient with metastatic estrogen receptor- positive, her2-negative breast cancer with CDKN2A loss who experienced a clinical response to palbociclib.

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