PONATINIB FOR THE TREATMENT OF CHRONIC MYELOID LEUKEMIA AND PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA

被引:6
作者
Narayanan, V. [1 ]
Pollyea, D. A. [1 ,2 ]
Gutman, J. A. [1 ,2 ]
Jimeno, A. [1 ,2 ]
机构
[1] Univ Colorado, Sch Med, Dept Med, Div Med Oncol, Aurora, CO 80045 USA
[2] Univ Colorado, Sch Med, Dev Therapeut Program, Aurora, CO 80045 USA
关键词
Ponatinib; Chronic myeloid leukemia; Acute lymphoblastic leukemia; Tyrosine kinase inhibitor; T315I mutation; CHRONIC MYELOGENOUS LEUKEMIA; PATIENTS RECEIVING IMATINIB; KINASE DOMAIN MUTATIONS; ABL TYROSINE KINASE; CHRONIC-PHASE; CANCER STATISTICS; FOLLOW-UP; INHIBITOR; RESISTANCE; GENE;
D O I
10.1358/dot.2013.49.4.1950147
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ponatinib is a novel, next-generation, small-molecule tyrosine kinase inhibitor with potent activity against the BCR-ABL fusion oncogene as well as all other ABL kinase domain mutations that confer resistance to earlier generation tyrosine kinase inhibitors. Due to its unique structure, it is the only tyrosine kinase inhibitor with the capability to counter the highly resistant T315I or gate-keeper mutation in leukemic cells that express the Philadelphia chromosome. This review will focus on the preclinical pharmacology, pharmacokinetics and clinical utility of ponatinib in the treatment of chronic myeloid leukemia and Philadelphia chromosome-positive adult acute lymphoblastic leukemia.
引用
收藏
页码:261 / 269
页数:9
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