the editor: Varying response to escalating the dose of imatinib in patients with CML who “acquire ” a BCR-ABLM244V mutant allele We report results of monitoring BCR-ABL transcript levels in 6 patients with chronic myeloid leukemia (CML) treated with imatinib mesylate (IM) who were found to have the same BCR-ABLM244V mutant allele. In vitro data suggest that this mutation is moderately resistant to IM, with an inhibitory concentration at 50 % (IC50) of 4.1 M,1 and that resistance may be overcome by dose escalation.2,3 In practice, the response to increasing the doses of IM varied in the 6 patients (Figure 1), an observation that can be interpreted in 1 of 3 ways: (1) the degree to which the mutation confers resistance to IM is very variable ...
<p>Mutation status of 36 chronic myeloid leukemia (CML) patients in chronic phase with primary and s...
Imatinib (IM) resistance occurs in cells from chronic myelogenous leukemia (CML) patients. Resistanc...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibito...
Purpose: Point mutations within the ABL kinase domain of the BCR-ABL gene have been associated with ...
PURPOSE: Point mutations within the ABL kinase domain of the BCR-ABL gene have been associated with ...
Background: The vast majority of chronic myeloid leukemia (CML) patients express the BCR-ABL transcr...
Second-generation tyrosine kinase inhibitors induce cytogenetic responses in approxi-mately 50 % of ...
The introduction of selective tyrosine-kinase inhibitors (TKIs) for the treatment of chronic myeloid...
PURPOSE: Nilotinib is a second-generation tyrosine kinase inhibitor indicated for the treatment of p...
CML is a myeloproliferative disease characterized by the Phila-delphia (Ph) chromosome, in which the...
the editor: BCR-ABL expression in leukemic progenitors and primitive stem cells of patients with chr...
Resistance to imatinib is commonly associated with reactivation of BCR-ABL signaling. Many such pati...
In imatinib-treated chronic myeloid leuke-mia (CML), secondary drug resistance is often caused by mu...
none2siIn patients with chronic myeloid leukemia (CML) resistant to imatinib, resistance is commonly...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibitor...
<p>Mutation status of 36 chronic myeloid leukemia (CML) patients in chronic phase with primary and s...
Imatinib (IM) resistance occurs in cells from chronic myelogenous leukemia (CML) patients. Resistanc...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibito...
Purpose: Point mutations within the ABL kinase domain of the BCR-ABL gene have been associated with ...
PURPOSE: Point mutations within the ABL kinase domain of the BCR-ABL gene have been associated with ...
Background: The vast majority of chronic myeloid leukemia (CML) patients express the BCR-ABL transcr...
Second-generation tyrosine kinase inhibitors induce cytogenetic responses in approxi-mately 50 % of ...
The introduction of selective tyrosine-kinase inhibitors (TKIs) for the treatment of chronic myeloid...
PURPOSE: Nilotinib is a second-generation tyrosine kinase inhibitor indicated for the treatment of p...
CML is a myeloproliferative disease characterized by the Phila-delphia (Ph) chromosome, in which the...
the editor: BCR-ABL expression in leukemic progenitors and primitive stem cells of patients with chr...
Resistance to imatinib is commonly associated with reactivation of BCR-ABL signaling. Many such pati...
In imatinib-treated chronic myeloid leuke-mia (CML), secondary drug resistance is often caused by mu...
none2siIn patients with chronic myeloid leukemia (CML) resistant to imatinib, resistance is commonly...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibitor...
<p>Mutation status of 36 chronic myeloid leukemia (CML) patients in chronic phase with primary and s...
Imatinib (IM) resistance occurs in cells from chronic myelogenous leukemia (CML) patients. Resistanc...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibito...