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ABSTRACT: Background
We report the clinical activity, safety, and identification of a predictive biomarker for bintrafusp alfa, a first-in-class bifunctional fusion protein composed of the extracellular domain of TGFβRII (a TGF-β "trap") fused to a human IgG1 mAb blocking PD-L1, in patients with advanced triple-negative breast cancer (TNBC).Methods
In this expansion cohort of a global phase 1 study, patients with pretreated, advanced TNBC received bintrafusp alfa 1200 mg every 2 weeks intravenously until disease progression, unacceptable toxicity, or withdrawal. The primary objective was confirmed best overall response by RECIST 1.1 assessed per independent review committee (IRC).Results
As of May 15, 2020, a total of 33 patients had received bintrafusp alfa, for a median of
SUBMITTER: Spira A
PROVIDER: S-EPMC9773992 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature