作者: Sandrine Hayette , Kaddour Chabane , Mauricette Michallet , Estelle Michallat , Pascale Cony-Makhoul
DOI: 10.1016/J.LEUKRES.2010.06.030
关键词:
摘要: This report aims to more accurately define the frequency of involvement SRC Family Kinases (SFKs) in imatinib- and dasatinib-resistant CML patients. Clinical samples were analysed during vivo treatment. We confirmed high SFKs Tyrosine kinase inhibitor-resistant (52% cases) even further progressive disease blast crises (60% cases). The deregulation is also observed patients harboring BCR-ABL mutations. In T315I F317L mutated patients, CML-resistance appears be promoted by protein reactivation once clone has decreased on Omacetaxine.