Combination venetoclax and selinexor effective in relapsed refractory multiple myeloma with translocation t(11;14)

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作者
Nina Nguyen
Sana Chaudhry
Tulasigeri M. Totiger
Robert Diaz
Evan Roberts
Skye Montoya
Gabriel Pardo
Alejandro Pardo
Jumana Afaghani
Maurizio Affer
Jacob Jahn
Terrence Bradley
Francesco Maura
Dickran Kazandjian
Daniel Bilbao
Jennifer Chapman
Ola Landgren
James Hoffman
Justin Taylor
机构
[1] Sylvester Comprehensive Cancer Center at the University of Miami Miller School of Medicine,Leukemia Program, Department of Medicine
[2] University of Miami Miller School of Medicine,Myeloma Division, Department of Medicine
[3] University of Miami Miller School of Medicine,Department of Pathology
[4] University of Miami Miller School of Medicine,undefined
来源
npj Precision Oncology | / 6卷
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摘要
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.
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[1]  
Bergsagel PL(1996)Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma Proc. Natl Acad. Sci. USA 93 13931-13936
[2]  
Fonseca R(2002)Myeloma and the t(11;14)(q13;q32); evidence for a biologically defined unique subset of patients Blood 99 3735-3741
[3]  
Lakshman A(2018)Natural history of t(11;14) multiple myeloma Leukemia 32 131-138
[4]  
Specht K(2004)Different mechanisms of cyclin D1 overexpression in multiple myeloma revealed by fluorescence in situ hybridization and quantitative analysis of mRNA levels Blood 104 1120-1126
[5]  
Touzeau C(2014)The Bcl-2 specific BH3 mimetic ABT-199: a promising targeted therapy for t(11;14) multiple myeloma Leukemia 28 210-212
[6]  
Touzeau C(2018)Targeting Bcl-2 for the treatment of multiple myeloma Leukemia 32 1899-1907
[7]  
Maciag P(2021)Targeting epigenetic mechanisms to overcome venetoclax resistance Biochim. Biophys. Acta Mol. Cell Res. 1868 119047-1642
[8]  
Amiot M(2020)Venetoclax or placebo in combination with bortezomib and dexamethasone in patients with relapsed or refractory multiple myeloma (BELLINI): a randomised, double-blind, multicentre, phase 3 trial Lancet Oncol. 21 1630-345
[9]  
Moreau P(2018)Clinical implications of targeting XPO1-mediated nuclear export in multiple myeloma Clin. Lymphoma Myeloma Leuk. 18 335-3114
[10]  
Prado G(2000)Phosphorylation-dependent regulation of cyclin D1 nuclear export and cyclin D1-dependent cellular transformation Genes Dev. 14 3102-56066