The purpose was to assess predictive factors for outcome in patients with chronic myeloid leukemia (CML) in chronic phase (CML-CP) treated with nilotinib after imatinib failure. Imatinib-resistant and -intolerant patients with CML-CP (n = 321) were treated with nilotinib 400 mg twice daily. Of 19 baseline patient and disease characteristics and two response end points analyzed, 10 independent prognostic factors were associated with progression-free survival (PFS). In the multivariate analysis, major cytogenetic response (MCyR) within 12 months, baseline hemoglobin >= 120 g/l, baseline basophils <4%, and absence of baseline mutations with low sensitivity to nilotinib were associated with PFS. A prognostic score was created to s...
Nilotinib (Tasigna) is a BCR-ABL1 tyrosine kinase inhibitor approved for the treatment of patients w...
Ronan Swords, Devalingam Mahalingam, Swaminathan Padmanabhan, Jennifer Carew, Francis GilesInstitute...
Background Second-generation tyrosine kinase inhibitors induce cytogenetic responses in approximatel...
The purpose was to assess predictive factors for outcome in patients with chronic myeloid leukemia (...
Background: Nilotinib is a potent and selective BCR-ABL inhibitor approved for use in patients with ...
<p><b>Objective:</b> Until recently, imatinib was the standard first-line treatment in chronic myelo...
PURPOSE: The association between initial molecular response and longer-term outcomes with nilotinib ...
Nilotinib is a highly selective Bcr-Abl inhibitor approved for imatinib-resistant chronic myeloid le...
Nilotinib has a higher binding affinity and selectivity for BCR-ABL with respect to imatinib and is ...
BACKGROUND: Nilotinib is active in imatinib-resistant and -intolerant chronic myeloid leukemia patie...
Nilotinib (Tasigna) is a BCR-ABL1 tyrosine kinase inhibitor approved for the treatment of patients w...
Nilotinib is a potent selective inhibitor of the BCR-ABL tyrosine kinase approved for use in patient...
Nilotinib (Tasigna) is a potent and selective BCR-ABL inhibitor approved for use in patients with ne...
Nilotinib has a higher binding affinity and selectivity for BCR-ABL with respect to imatinib and is ...
Nilotinib has a higher binding affinity and selectivity for BCR-ABL with respect to imatinib and is ...
Nilotinib (Tasigna) is a BCR-ABL1 tyrosine kinase inhibitor approved for the treatment of patients w...
Ronan Swords, Devalingam Mahalingam, Swaminathan Padmanabhan, Jennifer Carew, Francis GilesInstitute...
Background Second-generation tyrosine kinase inhibitors induce cytogenetic responses in approximatel...
The purpose was to assess predictive factors for outcome in patients with chronic myeloid leukemia (...
Background: Nilotinib is a potent and selective BCR-ABL inhibitor approved for use in patients with ...
<p><b>Objective:</b> Until recently, imatinib was the standard first-line treatment in chronic myelo...
PURPOSE: The association between initial molecular response and longer-term outcomes with nilotinib ...
Nilotinib is a highly selective Bcr-Abl inhibitor approved for imatinib-resistant chronic myeloid le...
Nilotinib has a higher binding affinity and selectivity for BCR-ABL with respect to imatinib and is ...
BACKGROUND: Nilotinib is active in imatinib-resistant and -intolerant chronic myeloid leukemia patie...
Nilotinib (Tasigna) is a BCR-ABL1 tyrosine kinase inhibitor approved for the treatment of patients w...
Nilotinib is a potent selective inhibitor of the BCR-ABL tyrosine kinase approved for use in patient...
Nilotinib (Tasigna) is a potent and selective BCR-ABL inhibitor approved for use in patients with ne...
Nilotinib has a higher binding affinity and selectivity for BCR-ABL with respect to imatinib and is ...
Nilotinib has a higher binding affinity and selectivity for BCR-ABL with respect to imatinib and is ...
Nilotinib (Tasigna) is a BCR-ABL1 tyrosine kinase inhibitor approved for the treatment of patients w...
Ronan Swords, Devalingam Mahalingam, Swaminathan Padmanabhan, Jennifer Carew, Francis GilesInstitute...
Background Second-generation tyrosine kinase inhibitors induce cytogenetic responses in approximatel...