| Literature DB >> 18436994 |
Marta Barańska1, Krzysztof Lewandowski, Michał Gniot, Małgorzata Iwoła, Maria Lewandowska, Mieczysław Komarnicki.
Abstract
Point mutations of bcr-abl tyrosine kinase are the most frequent causes of imatinib resistance in chronic myeloid leukaemia (CML) patients. In most CML cases with BCR-ABL mutations leading to imatinib resistance the second generation of tyrosine kinase inhibitors (TKI- e.g. nilotinib or dasatinib) may be effective. Here, we report a case of a CML patient who during imatinib treatment did not obtain clinical and cytogenetic response within 12 months of therapy. The sequencing of BCR-ABL kinase domains was performed and revealed the presence of a F359I point mutation (TTC-to-ATC nucleotide change leading to Phe-to-Ile amino acid substitution). After 1 month of nilotinib therapy a rapid progression of clinical symptoms was observed. In the presence of the F359I point mutation only dasatinib treatment overcame imatinib and nilotinib resistance.Entities:
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Year: 2008 PMID: 18436994 DOI: 10.1007/BF03195613
Source DB: PubMed Journal: J Appl Genet ISSN: 1234-1983 Impact factor: 3.240