| Literature DB >> 21279819 |
Masaya Okada1, Atsushi Satake1, Katsuji Kaida1, Kyoko Taniguchi1, Satoshi Yoshihara1, Kazuhiro Ikegame1, Hiroya Tamaki1,2, Toshihiro Soma1, Yoshihiro Fujimori3, Hiroyasu Ogawa1,2.
Abstract
Chronic myelogenous leukemia (CML) is characterized by Philadelphia (Ph) chromosome with a chimeric gene BCR-ABL created by reciprocal t(9:22) (q34;q11) translocation. Variant Ph chromosome translocations involving chromosomes other than 9 and 22 are found in 5-10% of CML cases. We here report a CML patient who carries a four-way Ph chromosome translocation, t(9;22;15;19) (q34;q11;q15;q13). The patient was diagnosed in 1997 and initially treated with hydroxyurea. In 2002, treatment with imatinib, a selective BCR-ABL tyrosine kinase inhibitor (TKI), was started but Ph-positive chromosomes remained at the levels of 42-65%, indicating imatinib failure. In 2006, the point mutations of F359I and L387M were detected in BCR/ABL gene, which may be related to imatinib failure. Treatment with nilotinib, a TKI with high target specificity, was then started which resulted in durable major molecular response. Administration of nilotinib offered an effective treatment in a CML patient with variant Ph chromosome translocations and BCR-ABL point mutations after imatinib failure.Entities:
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Year: 2011 PMID: 21279819 DOI: 10.1007/s12185-011-0769-z
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490