Source:http://linkedlifedata.com/resource/pubmed/id/19519355
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2009-6-12
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pubmed:abstractText |
Imatinib mesylate is currently the standard therapy for chronic myeloid leukemia (CML) patients. Despite the remarkable results achieved with imatinib, the emergence of resistance to this drug has become a significant problem. Several strategies have been developed to overcome imatinib resistance, including dose escalation of the drug, combination treatments or novel targeted agents. Nilotinib is a second-generation tyrosine kinase inhibitor 30-50 fold more potent than imatinib with high affinity and selectivity on BCR/ABL, active against a wide range of mutant clones, except T315I mutation. Phase II trials of nilotinib showed high activity in imatinib-resistant or intolerant CML patients; front-line treatment of chronic phase Ph+ CML demonstrated rapid and stable cytogenetic responses and increasing molecular responses. We here review the development of nilotinib and the efficacy data in phase II and front-line trials.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/4-methyl-N-(3-(4-methylimidazol-1-yl...,
http://linkedlifedata.com/resource/pubmed/chemical/Fusion Proteins, bcr-abl,
http://linkedlifedata.com/resource/pubmed/chemical/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidines,
http://linkedlifedata.com/resource/pubmed/chemical/imatinib
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1873-5592
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
530-6
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pubmed:meshHeading |
pubmed-meshheading:19519355-Animals,
pubmed-meshheading:19519355-Clinical Trials as Topic,
pubmed-meshheading:19519355-Drug Resistance, Neoplasm,
pubmed-meshheading:19519355-Drug Synergism,
pubmed-meshheading:19519355-Fusion Proteins, bcr-abl,
pubmed-meshheading:19519355-Humans,
pubmed-meshheading:19519355-Leukemia, Myelogenous, Chronic, BCR-ABL Positive,
pubmed-meshheading:19519355-Piperazines,
pubmed-meshheading:19519355-Protein Kinase Inhibitors,
pubmed-meshheading:19519355-Pyrimidines
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pubmed:year |
2009
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pubmed:articleTitle |
Nilotinib therapy in chronic myelogenous leukemia: the strength of high selectivity on BCR/ABL.
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pubmed:affiliation |
Department of Cellular Biotechnologies and Hematology, University La Sapienza, Rome, Italy. breccia@bce.uniroma1.it
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pubmed:publicationType |
Journal Article,
Review
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