Purpose: In the first years of imatinib treatment, BCR-ABL remained detectable in all but a small minority of patients with chronic myeloid leukemia. We determined whether BCR-ABL continues to decline with longer imatinib exposure and the incidence and consequence of undetectable BCR-ABL. Experimental Design: BCR-ABL levels were measured in a subset of 53 imatinib-treated IRIS trial patients for up to 7 years (29 first-line, 24 second-line). Levels were deemed undetectable using strict PCR sensitivity criteria. Results: By 18 months, the majority achieved a 3-log reduction [major molecular response (MMR)]. BCR-ABL continued to decline but at a slower rate (median time to 4-log reduction and undetectable BCR-ABL of 45 and 66 months for first...
Around 50% of chronic myeloid leukaemia (CML) patients who remain on imatinib treatment for more tha...
In imatinib-treated chronic myeloid leuke-mia (CML), secondary drug resistance is often caused by mu...
PURPOSE: Imatinib mesylate is a potent inhibitor of BCR-ABL, the constitutively active tyrosine kina...
Early reduction of BCR-ABL1 transcript levels has been associated with improved outcome in chronic m...
© 2009 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.We a...
Recent studies have demonstrated that some patients with chronic myeloid leukemia (CML) can maintain...
PURPOSE: The association between initial molecular response and longer-term outcomes with nilotinib ...
We sought to determine dynamics of BCR-ABL mRNA expression levels in 139 patients with chronic myelo...
Background: The advent of imatinib has considerably changed the treatment of chronic myeloid leukemi...
BACKGROUND: Real time PCR has become the most common technique to monitor BCR-ABL transcript levels ...
BACKGROUND: Real time PCR has become the most common technique to monitor BCR-ABL transcript levels ...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Early reduction of BCR-ABL1 transcript ...
A reduction in BCR-ABL1/ABL1IS transcript levels to <10% after 3 months or <1% after 6 months ...
Purpose: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatinib achiev...
Purpose: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatinib achiev...
Around 50% of chronic myeloid leukaemia (CML) patients who remain on imatinib treatment for more tha...
In imatinib-treated chronic myeloid leuke-mia (CML), secondary drug resistance is often caused by mu...
PURPOSE: Imatinib mesylate is a potent inhibitor of BCR-ABL, the constitutively active tyrosine kina...
Early reduction of BCR-ABL1 transcript levels has been associated with improved outcome in chronic m...
© 2009 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.We a...
Recent studies have demonstrated that some patients with chronic myeloid leukemia (CML) can maintain...
PURPOSE: The association between initial molecular response and longer-term outcomes with nilotinib ...
We sought to determine dynamics of BCR-ABL mRNA expression levels in 139 patients with chronic myelo...
Background: The advent of imatinib has considerably changed the treatment of chronic myeloid leukemi...
BACKGROUND: Real time PCR has become the most common technique to monitor BCR-ABL transcript levels ...
BACKGROUND: Real time PCR has become the most common technique to monitor BCR-ABL transcript levels ...
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Early reduction of BCR-ABL1 transcript ...
A reduction in BCR-ABL1/ABL1IS transcript levels to <10% after 3 months or <1% after 6 months ...
Purpose: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatinib achiev...
Purpose: Most patients with chronic-phase chronic myeloid leukemia (CML) who receive imatinib achiev...
Around 50% of chronic myeloid leukaemia (CML) patients who remain on imatinib treatment for more tha...
In imatinib-treated chronic myeloid leuke-mia (CML), secondary drug resistance is often caused by mu...
PURPOSE: Imatinib mesylate is a potent inhibitor of BCR-ABL, the constitutively active tyrosine kina...