首页> 外文OA文献 >Drug resistance and BCR-ABL kinase domain mutations in Philadelphia chromosome-positive acute lymphoblastic leukemia from the imatinib to the second-generation tyrosine kinase inhibitor era: The main changes are in the type of mutations, but not in the frequency of mutation involvement
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Drug resistance and BCR-ABL kinase domain mutations in Philadelphia chromosome-positive acute lymphoblastic leukemia from the imatinib to the second-generation tyrosine kinase inhibitor era: The main changes are in the type of mutations, but not in the frequency of mutation involvement

机译:从伊马替尼到第二代酪氨酸激酶抑制剂时代的费城染色体阳性急性淋巴细胞白血病的耐药性和BCR-ABL激酶结构域突变:主要变化在于突变类型,但不涉及突变发生的频率

摘要

Patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) frequently relapse on imatinib with acquisition of BCR-ABL kinase domain (KD) mutations. To analyze the changes that second-generation tyrosine kinase inhibitors (TKIs) have brought in mutation frequency and type, a database review was undertaken of the results of all the BCR-ABL KD mutation analyses performed in the authors' laboratory from January 2004 to January 2013.
机译:费城染色体阳性(Ph +)急性淋巴细胞白血病(ALL)的患者经常因获得BCR-ABL激酶结构域(KD)突变而在伊马替尼上复发。为了分析第二代酪氨酸激酶抑制剂(TKIs)导致突变频率和类型的变化,对作者于2004年1月至1月在实验室进行的所有BCR-ABL KD突变分析的结果进行了数据库审查。 2013。

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