| Literature DB >> 24131888 |
Simona Soverini1, Susan Branford2, Franck E Nicolini3, Moshe Talpaz4, Michael W N Deininger5, Giovanni Martinelli6, Martin C Müller7, Jerald P Radich8, Neil P Shah9.
Abstract
Patients with chronic myeloid leukemia develop resistance to both first-generation and second-generation tyrosine kinase inhibitors (TKIs) as a result of mutations in the kinase domain (KD) of BCR-ABL1. A wide range of BCR-ABL1 KD mutations that confer resistance to TKIs have been identified, and the T315I mutant has proven particularly difficult to target. This review summarizes the prevalence, impact, and prognostic implications of BCR-ABL1 KD mutations in patients with chronic myeloid leukemia who are treated with current TKIs and provides an overview of recent treatment guidelines and future trends for the detection of mutations.Entities:
Keywords: BCR-ABL1; Chronic myeloid leukemia; Kinase domain; Mutations; Philadelphia chromosome; Resistance; Tyrosine kinase inhibitors
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Year: 2013 PMID： 24131888 DOI： 10.1016/j.leukres.2013.09.011
Source DB: PubMed Journal: Leuk Res ISSN： 0145-2126 Impact factor: 3.156