Mechanisms of Resistance to ABL Kinase Inhibition in Chronic Myeloid Leukemia and the Development of Next Generation ABL Kinase Inhibitors

被引:133
|
作者
Patel, Ami B. [1 ]
O'Hare, Thomas [2 ]
Deininger, Michael W. [2 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Dept Hematol & Oncol, 2000 Circle Hope Dr, Salt Lake City, UT 84112 USA
[2] Univ Utah, Huntsman Canc Inst, Div Hematol & Hematol Malignancies, 2000 Circle Hope Dr, Salt Lake City, UT 84112 USA
关键词
Chronic myeloid leukemia (CML); Tyrosine kinase inhibitor (TKI); BCR-ABL1; Treatment-free remission (TFR); Drug resistance; Mutation; CHRONIC MYELOGENOUS LEUKEMIA; CML STEM-CELLS; LOW OCT-1 ACTIVITY; BCR-ABL; CHRONIC-PHASE; IMATINIB-RESISTANT; DOMAIN MUTATIONS; CLINICAL RESISTANCE; BETA-CATENIN; PEGINTERFERON ALPHA-2A;
D O I
10.1016/j.hoc.2017.04.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chronic myeloid leukemia is increasingly viewed as a chronic illness; most patients have a life expectancy close to that of the general population. Despite progress made using BCR-ABL1 tyrosine kinase inhibitors (TKIs), drug resistance via BCR-ABL1 dependent and BCR-ABL1 independent mechanisms continues to be an issue. BCR-ABL1 dependent resistance is primarily mediated through oncoprotein kinase domain mutations and usually results in overt resistance to TKIs. However, BCR-ABL1 independent resistance in the setting of effective BCR-ABL1 inhibition is recognized as a major contributor to minimal residual disease. Efforts to eradicate persistent leukemic stem cells have focused on combination therapy.
引用
收藏
页码:589 / +
页数:25
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