威尼斯人
多发性骨髓瘤
医学
染色体易位
癌症研究
人口
联合疗法
耐火材料(行星科学)
肿瘤科
药理学
内科学
白血病
生物
基因
环境卫生
天体生物学
慢性淋巴细胞白血病
生物化学
作者
Nina Nguyen,Sana Chaudhry,Tulasigeri M. Totiger,Robert Diaz,Evan R. Roberts,Skye Montoya,Gabriel Pardo,Alejandro Pardo,Jumana Afaghani,Maurizio Affer,Jacob Jahn,Terrence Bradley,Francesco Maura,Dickran Kazandjian,Daniel Bilbao,Jennifer R. Chapman,Ola Landgren,James E. Hoffman,Justin Taylor
标识
DOI:10.1038/s41698-022-00315-2
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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