伊布替尼
布鲁顿酪氨酸激酶
慢性淋巴细胞白血病
生物
酪氨酸激酶
白血病
癌症研究
免疫学
受体
遗传学
作者
Marcel Spaargaren,M F M de Rooij,Arnon P. Kater,Eric Eldering
出处
期刊:Oncogene
[Springer Nature]
日期:2014-06-23
卷期号:34 (19): 2426-2436
被引量:28
摘要
The treatment of chronic lymphocytic leukemia (CLL) with inhibitors targeting B cell receptor signaling and other survival mechanisms holds great promise. Especially the early clinical success of Ibrutinib, an irreversible inhibitor of Bruton’s tyrosine kinase (BTK), has received widespread attention. In this review we will focus on the fundamental and clinical aspects of BTK inhibitors in CLL, with emphasis on Ibrutinib as the best studied of this class of drugs. Furthermore, we summarize recent laboratory as well as clinical findings relating to the first cases of Ibrutinib resistance. Finally, we address combination strategies with Ibrutinib, and attempt to extrapolate its current status to the near future in the clinic.
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