The safety of Bruton's tyrosine kinase inhibitors for the treatment of chronic lymphocytic leukemia

被引:9
作者
Tran, Phu N. [1 ]
O'Brien, Susan [1 ]
机构
[1] Univ Calif Irvine, Div Hematol Oncol, Orange, CA 92668 USA
关键词
BTK inhibitors; chronic lymphocytic leukemia; ibrutinib; chemoimmunotherapy; safety; toxicity; IBRUTINIB TREATMENT; AUTOIMMUNE CYTOPENIAS; ATRIAL-FIBRILLATION; THERAPEUTIC TARGET; DURABLE RESPONSES; SIGNALING PATHWAY; FREE SURVIVAL; 17P DELETION; OPEN-LABEL; ACTIVATION;
D O I
10.1080/14740338.2017.1344213
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The approval of ibrutinib has revolutionized the therapeutic landscape of chronic lymphocytic leukemia (CLL). Currently ibrutinib is indicated for patients that are both treatment naive as well as those with relapsed CLL. Ibrutinib is generally well-tolerated with durable responses that improve over time in most patients. Important toxicities include atrial fibrillation and bleeding. Areas cover: This review covers the pharmacokinetics, pharmacodynamics, safety and efficacy of ibrutinib in the treatment of CLL. We also compare ibrutinib with other kinase inhibitors and chemoimmunotherapy regimens using data from clinical trials. A literature search utilized the PubMed database. Expert opinion: Despite the efficacy and tolerability of ibrutinib, important questions remain, which include selection of patients receiving ibrutinib in the first and subsequent lines of treatment, optimal dosing, sequential use of ibrutinib versus other kinase inhibitors and combination therapy. Prospective studies should incorporate minimal residual disease (MRD) status as a clinical endpoint to determine whether patients can be taken off kinase inhibitors.
引用
收藏
页码:1079 / 1088
页数:10
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