| Literature DB >> 35876604 |
Amy K LeBlanc1, Christina N Mazcko1, Timothy M Fan2,3, David M Vail4, Brian K Flesner5, Jeffrey N Bryan5,6, Shan Li7, Feng Wang7, Scott Harris8, Jesse D Vargas8, Jeevan P Govindharajulu9, Soumya Jaganathan9, Francesca Tomaino9, Apurva K Srivastava9, Tsui-Fen Chou7, Gordon M Stott10, Joseph M Covey11, Barbara Mroczkowski11, James H Doroshow11.
Abstract
Pet dogs with naturally occurring cancers play an important role in studies of cancer biology and drug development. We assessed tolerability, efficacy, and pharmacokinetic/pharmacodynamic relationships with a first-in-class small molecule inhibitor of valosin-containing protein (VCP/p97), CB-5339, administered to 24 tumor-bearing pet dogs. Tumor types assessed included solid malignancies, lymphomas, and multiple myeloma. Through a stepwise dose and schedule escalation schema, we determined the maximum tolerated dose to be 7.5 mg/kg when administered orally on a 4 days on, 3 days off schedule per week for 3 consecutive weeks. Adverse events were minimal and mainly related to the gastrointestinal system. Pharmacokinetic/pharmacodynamic data suggest a relationship between exposure and modulation of targets related to induction of the unfolded protein response, but not to tolerability of the agent. An efficacy signal was detected in 33% (2/6) of dogs with multiple myeloma, consistent with a mechanism of action relating to induction of proteotoxic stress in a tumor type with abundant protein production. Clinical trials of CB-5339 in humans with acute myelogenous leukemia and multiple myeloma are ongoing. ©2022 The Authors; Published by the American Association for Cancer Research.Entities:
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Year: 2022 PMID: 35876604 PMCID: PMC9538592 DOI: 10.1158/1535-7163.MCT-22-0167
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.009