| Literature DB >> 36261486 |
Nina Nguyen1, Sana Chaudhry1, Tulasigeri M Totiger1, Robert Diaz1, Evan Roberts1, Skye Montoya1, Gabriel Pardo1, Alejandro Pardo1, Jumana Afaghani1, Maurizio Affer1, Jacob Jahn1, Terrence Bradley2, Francesco Maura3, Dickran Kazandjian3, Daniel Bilbao1, Jennifer Chapman4, Ola Landgren3, James Hoffman5, Justin Taylor6.
Abstract
Patients with multiple myeloma-bearing translocation t(11;14) have recently been shown to benefit from the apoptosis-inducing drug venetoclax; however, the drug lacks FDA approval in multiple myeloma thus far due to a potential safety signal in the overall patient population. Selinexor is an inhibitor of nuclear export that is FDA-approved for patients with multiple myeloma refractory to multiple lines of therapy. Here, we report that in four patients with multiple myeloma with t(11;14), the concomitant administration of venetoclax and selinexor was safe and associated with disease response. Moreover, the combination was synergistic in t(11;14) multiple myeloma cell lines and caused decreased levels of Cyclin D1 (which is overexpressed due to the CCND1-IGH fusion) when given in combination as compared to single agents. These data suggest that the combination of venetoclax and selinexor is effective and t(11;14) may serve as a therapeutic marker for response and target for future clinical trials.Entities:
Year: 2022 PMID: 36261486 PMCID: PMC9581939 DOI: 10.1038/s41698-022-00315-2
Source DB: PubMed Journal: NPJ Precis Oncol ISSN: 2397-768X