The treatment outcome and development of new mutations in patients with imatinib- and/or nilotinib-failure Philadelphia chromosome positive (Ph+) leukemia with highly nilotinib-resistant mutations (Y253H, E255K/V and F359V/C) were assessed on dasatinib therapy. A total of 111 patients with Ph+ leukemia were grouped into three cohorts by baseline BCR-ABL kinase domain mutation status: no mutation (n = 44), non-nilotinib-resistant mutations (n = 26) or nilotinib-resistant mutations (n = 41). The frequencies of hematological, cytogenetic and molecular responses and clinical resistance to dasatinib were similar among the three cohorts during dasatinib therapy. In dasatinib-resistant patients, new mutations were most frequently observed in the c...
Despite the beneficial effects of imatinib mesylate, some patients may either not respond or respond...
In Philadelphia-positive (Ph+) acute lymphoblastic leukemia (ALL) patients (pts) treated with tyrosi...
Mutations in the kinase domain (KD) of BCR-ABL are the most prevalent mechanism of acquired resistan...
Dasatinib and nilotinib are tyrosine kinase inhibitors (TKIs) developed to overcome imatinib resista...
Incorporation of the tyrosine kinase inhibitor (TKI) imatinib in the frontline treatment of Philadel...
The emergence of resistance to the Bcr-Abl inhibitor imatinib mesylate in patients with Philadelphia...
Patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) frequently r...
Patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) frequently r...
none19noNo abstract available.mixedS. Soverini;G. Martinelli;S. Colarossi;A. Gnani;F. Castagnetti;G....
Specific imatinib-resistant BCR-ABL1 mutations (Y253H, E255K/V, T315I, F317L, and F359V/C) predict f...
The advent of imatinib, a potent and selective inhibitor of the Bcr-Abl tyrosine kinase whose deregu...
Background and Aims. Mutations in the Bcr-Abl kinase domain (KD) are often detected at the time of r...
The BCR-ABL T315I mutation causes resistance to imatinib, nilotinib and dasatinib in chronic myeloid...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibitor...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibito...
Despite the beneficial effects of imatinib mesylate, some patients may either not respond or respond...
In Philadelphia-positive (Ph+) acute lymphoblastic leukemia (ALL) patients (pts) treated with tyrosi...
Mutations in the kinase domain (KD) of BCR-ABL are the most prevalent mechanism of acquired resistan...
Dasatinib and nilotinib are tyrosine kinase inhibitors (TKIs) developed to overcome imatinib resista...
Incorporation of the tyrosine kinase inhibitor (TKI) imatinib in the frontline treatment of Philadel...
The emergence of resistance to the Bcr-Abl inhibitor imatinib mesylate in patients with Philadelphia...
Patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) frequently r...
Patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) frequently r...
none19noNo abstract available.mixedS. Soverini;G. Martinelli;S. Colarossi;A. Gnani;F. Castagnetti;G....
Specific imatinib-resistant BCR-ABL1 mutations (Y253H, E255K/V, T315I, F317L, and F359V/C) predict f...
The advent of imatinib, a potent and selective inhibitor of the Bcr-Abl tyrosine kinase whose deregu...
Background and Aims. Mutations in the Bcr-Abl kinase domain (KD) are often detected at the time of r...
The BCR-ABL T315I mutation causes resistance to imatinib, nilotinib and dasatinib in chronic myeloid...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibitor...
PURPOSE: ABL kinase domain mutations have been implicated in the resistance to the BCR-ABL inhibito...
Despite the beneficial effects of imatinib mesylate, some patients may either not respond or respond...
In Philadelphia-positive (Ph+) acute lymphoblastic leukemia (ALL) patients (pts) treated with tyrosi...
Mutations in the kinase domain (KD) of BCR-ABL are the most prevalent mechanism of acquired resistan...