Towards Targeted Therapy of Chronic Lymphocytic Leukemia

被引:12
|
作者
Niemann, Carsten U. [1 ]
Jones, Jade [1 ]
Wiestner, Adrian [1 ]
机构
[1] NHLBI, Hematol Branch, NIH, Bethesda, MD 20892 USA
来源
ADVANCES IN CHRONIC LYMPHOCYTIC LEUKEMIA | 2013年 / 792卷
关键词
BCR (B cell antigen receptor); Microenvironment; Targeted therapy; Lymphocytosis; Ibrutinib (PCI-32765); idelalisib; (GS-1101; CAL-101); Everolimus (RAD001); Navitoclax (ABT-263); ABT-199; Lenalidomide; Dasatinib (BMS-354825); Fostamatinib (R788); BTK (Bruton's tyrosine kinase); SYK (spleen tyrosine kinase); LYN; PI3K (phosphatidylinositol 3 kinase); mTOR (mammalian target of rapamycin); BCL-2; B-CELL-RECEPTOR; TYROSINE KINASE INHIBITOR; PROGRESSION-FREE SURVIVAL; NON-HODGKIN-LYMPHOMA; ANTIGEN RECEPTOR; MAMMALIAN TARGET; CLL CELLS; FOSTAMATINIB DISODIUM; SIGNALING PATHWAYS; AUTOIMMUNE-DISEASE;
D O I
10.1007/978-1-4614-8051-8_12
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The B cell antigen receptor (BCR) and its downstream pathways are pivotal in the pathogenesis of chronic lymphocytic leukemia (CLL). Recently, inhibitors of kinases in the BCR pathway have shown promising clinical activity in CLL. Based upon these results, the treatment paradigm for CLL will likely undergo major changes. The kinases essential for BCR signal transduction, which are emerging as targets for CLL treatment, and the specific inhibitors under development are the focus of this chapter. In particular, the BTK inhibitor ibrutinib and the PI3K inhibitor idelalisib (GS-1101) are two evolving targeted therapies with the most mature clinical data.
引用
收藏
页码:259 / 291
页数:33
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