来那度胺
地塞米松
耐火材料(行星科学)
多发性骨髓瘤
医学
肿瘤科
药理学
核出口信号
癌症研究
内科学
生物
细胞核
天体生物学
精神科
核心
作者
Darrell White,Richard LeBlanc,Chritopher Venner,Nizar J. Bahlis,Suzanne Lentzsch,Cristina Gasparetto,Christine Chen,Brea Lipe,Heather J. Sutherland,Sascha A. Tuchman,Muhamed Baljević,Rami Kotb,Michaël Sébag,Nancy Callander,William Bensinger,Kazuharu Kai,Jianjun Liu,Heidi Sheehan,Daniel Nova Estepan,Jatin J. Shah,Gary J. Schiller
标识
DOI:10.1016/j.clml.2019.09.084
摘要
The nuclear export protein Exportin 1 (XPO1) is overexpressed in a wide variety of cancers including multiple myeloma. Selinexor (SEL) is a novel, first-in-class selective inhibitor of nuclear export (SINE), which blocks XPO1, forcing the nuclear retention and activation of tumor suppressor proteins. SEL in combination with dexamethasone (DEX) has demonstrated an overall response rate (ORR) of 26.2% in patients (pts) with triple class refractory MM. Lenalidomide (LEN) in combination with DEX is approved for the treatment of RRMM with an overall response rate (ORR) of 60-76%. The combination of SEL and LEN showed at least additive activity in preclinical models of MM. We therefore hypothesized that the all oral combination of SEL/LEN/DEX may result in improved response rates.
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