To investigate the impact of the combination of early molecular and cytogenetic responses on the achievement of MR4.5, 228 newly diagnosed chronic phase chronic myeloid leukemia patients treated with imatinib were categorized into 3-month and 6-month concordant optimal, discordant, concordant warning, and failure groups. Among them, 85.3% at 3 months and 78.1% at 6 months had concordant molecularly and cytogenetically defined responses. At both 3 and 6 months, patients with discordant, concordant warning and failure responses had similar 3-year MR4.5 rates, and all were significantly lower than the rate in patients with concordant optimal responses. Patients with concurrent 3-month and 6-month concordant optimal responses had a significantl...
Imatinib is a tyrosine-kinase inhibitor that binds to ABL proteins and induces cytogenetic remission...
PURPOSE: Imatinib mesylate is a potent inhibitor of BCR-ABL, the constitutively active tyrosine kina...
Achievement of complete molecular response in patients with chronic phase chronic myeloid leukemia h...
Introduction. The 2013 version of the European LeukemiaNet (ELN) recommendations for the management ...
To investigate the correlation of trough imatinib mesylate (IM) levels with cytogenetic or molecular...
none20noPURPOSE: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatini...
Purpose: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatinib achiev...
PURPOSE: The achievement of a major molecular response (MMolR) at 12 months is a surrogate marker of...
In the face of competing first-line treatment options for CML, early prediction of prognosis on imat...
CML patients who obtain a complete cytogenetic response (CCgR) may harbor different degrees of molec...
© 2009 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.We a...
The significance of molecular response depth is not well defined in patients with chronic phase chro...
Purpose: The achievement of a major molecular response (MMolR) at 12 months is a surrogate marker of...
To compare the clinical significance of 3-month cytogenetic and molecular monitoring, we analyzed 1,...
Background: Response dynamics in pts treated with nilotinib for imatinib failure may be different th...
Imatinib is a tyrosine-kinase inhibitor that binds to ABL proteins and induces cytogenetic remission...
PURPOSE: Imatinib mesylate is a potent inhibitor of BCR-ABL, the constitutively active tyrosine kina...
Achievement of complete molecular response in patients with chronic phase chronic myeloid leukemia h...
Introduction. The 2013 version of the European LeukemiaNet (ELN) recommendations for the management ...
To investigate the correlation of trough imatinib mesylate (IM) levels with cytogenetic or molecular...
none20noPURPOSE: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatini...
Purpose: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatinib achiev...
PURPOSE: The achievement of a major molecular response (MMolR) at 12 months is a surrogate marker of...
In the face of competing first-line treatment options for CML, early prediction of prognosis on imat...
CML patients who obtain a complete cytogenetic response (CCgR) may harbor different degrees of molec...
© 2009 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.We a...
The significance of molecular response depth is not well defined in patients with chronic phase chro...
Purpose: The achievement of a major molecular response (MMolR) at 12 months is a surrogate marker of...
To compare the clinical significance of 3-month cytogenetic and molecular monitoring, we analyzed 1,...
Background: Response dynamics in pts treated with nilotinib for imatinib failure may be different th...
Imatinib is a tyrosine-kinase inhibitor that binds to ABL proteins and induces cytogenetic remission...
PURPOSE: Imatinib mesylate is a potent inhibitor of BCR-ABL, the constitutively active tyrosine kina...
Achievement of complete molecular response in patients with chronic phase chronic myeloid leukemia h...