| Literature DB >> 28161886 |
Patricia M LoRusso1,2, Mrinal Gounder3, Shadia I Jalal4, Valérie André5, Siva Rama Prasad Kambhampati5, Nick Loizos5, Jennifer Hall5,6, Timothy R Holzer5, Aejaz Nasir5, Jan Cosaert5,7, John Kauh5, E Gabriela Chiorean4,8.
Abstract
Purpose Macrophage-stimulating 1-receptor (RON) is expressed on macrophages, epithelial cells, and a variety of tumors. Narnatumab (IMC-RON8; LY3012219) is a neutralizing monoclonal antibody that blocks RON binding to its ligand, macrophage-stimulating protein (MSP). This study assessed safety, maximum tolerated dose (MTD), pharmacokinetics, pharmacodynamics, and efficacy of narnatumab in patients with advanced solid tumors. Methods Narnatumab was administered intravenously weekly at 5, 10, 15, or 20 mg/kg or every 2 weeks at 15, 20, 30, or 40 mg/kg in 4-week cycles. Results Thirty-nine patients were treated, and 1 dose-limiting toxicity (DLT) (grade 3 hyponatremia, 5 mg/kg) was reported. The most common narnatumab-related adverse events (AEs) were fatigue (20.5%) and decreased appetite, diarrhea, nausea, and vomiting (10.3% each). Except for 2 treatment-related grade 3 AEs (hyponatremia, hypokalemia), all treatment-related AEs were grade 1 or 2. Narnatumab had a short half-life (<7 days). After Cycle 2, no patients had concentrations above 140 μg/mL (concentration that demonstrated antitumor activity in animal models), except for 1 patient receiving 30 mg/kg biweekly. Eleven patients had a best response of stable disease, ranging from 6 weeks to 11 months. Despite only 1 DLT, due to suboptimal drug exposure, the dose was not escalated beyond 40 mg/kg biweekly. This decision was based on published data reporting that mRNA splice variants of RON are highly prevalent in tumors, accumulate in cytoplasm, and are not accessible by large-molecule monoclonal antibodies. Conclusions Narnatumab was well tolerated and showed limited antitumor activity with this dosing regimen.Entities:
Keywords: IMC-RON8; Macrophage-stimulating protein receptor; Narnatumab; Phase 1; RON; Solid tumors
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Year: 2017 PMID: 28161886 PMCID: PMC5502198 DOI: 10.1007/s10637-016-0413-0
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850