| Literature DB >> 31822498 |
Brian D Lehmann1,2, Vandana G Abramson1,2, Melinda E Sanders3,4, Erica L Mayer5, Tufia C Haddad6, Rita Nanda7, Catherine Van Poznak8, Anna Maria Storniolo9, Julie R Nangia10, Paula I Gonzalez-Ericsson3,4, Violeta Sanchez11, Kimberly N Johnson2, Richard G Abramson12, Sheau-Chiann Chen13, Yu Shyr13, Carlos L Arteaga14, Antonio C Wolff15, Jennifer A Pietenpol.
Abstract
PURPOSE: Preclinical data demonstrating androgen receptor (AR)-positive (AR+) triple-negative breast cancer (TNBC) cells are sensitive to AR antagonists, and PI3K inhibition catalyzed an investigator-initiated, multi-institutional phase Ib/II study TBCRC032. The trial investigated the safety and efficacy of the AR-antagonist enzalutamide alone or in combination with the PI3K inhibitor taselisib in patients with metastatic AR+ (≥10%) breast cancer. PATIENTS AND METHODS: Phase Ib patients [estrogen receptor positive (ER+) or TNBC] with AR+ breast cancer received 160 mg enzalutamide in combination with taselisib to determine dose-limiting toxicities and the maximum tolerated dose (MTD). Phase II TNBC patients were randomized to receive either enzalutamide alone or in combination with 4 mg taselisib until disease progression. Primary endpoint was clinical benefit rate (CBR) at 16 weeks.Entities:
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Year: 2019 PMID: 31822498 PMCID: PMC7196503 DOI: 10.1158/1078-0432.CCR-19-2170
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531