Dasatinib treatment can overcome imatinib and nilotinib resistance in CML patient carrying F359I mutation of BCR-ABL oncogene

被引:19
作者
Baranska, Marta [1 ]
Lewandowski, Krzysztof [1 ]
Gniot, Michal [1 ]
Iwola, Malgorzata [1 ]
Lewandowska, Maria [1 ]
Komarnicki, Mieczyslaw [1 ]
机构
[1] Karol Marcinkowski Univ Med Sci, Dept Hematol, PL-60569 Poznan, Poland
关键词
BCR-ABL oncogene; chronic myeloid leukemia; direct sequencing; F359I point mutation; kinase inhibitors;
D O I
10.1007/BF03195613
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 I 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.
引用
收藏
页码:201 / 203
页数:3
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