ACUTE LYMPHOBLASTIC LEUKEMIA;
ALLOSTERISM;
ARTICLE;
CHRONIC MYELOID LEUKEMIA;
DRUG ABSORPTION;
DRUG DISTRIBUTION;
DRUG HALF LIFE;
DRUG PROTEIN BINDING;
DRUG TARGETING;
ENZYME CONFORMATION;
HUMAN;
NONHUMAN;
PENNSYLVANIA;
PHILADELPHIA CHROMOSOME POSITIVE CELL;
PRIORITY JOURNAL;
TUMOR XENOGRAFT;
ALLOSTERIC SITE;
ANALOGS AND DERIVATIVES;
ANIMAL;
ANTAGONISTS AND INHIBITORS;
CELL PROLIFERATION;
CHEMISTRY;
COMBINATION DRUG THERAPY;
DRUG EFFECTS;
DRUG RESISTANCE;
DRUG SCREENING;
ENZYME ACTIVE SITE;
ENZYMOLOGY;
GENETICS;
LEUKEMIA, MYELOGENOUS, CHRONIC, BCR-ABL POSITIVE;
MOUSE;
MUTATION;
PATHOLOGY;
Safety and efficacy of imatinib in CML over a period of 10 years: Data from the randomized CML-study IV
Kalmanti, L. et al. Safety and efficacy of imatinib in CML over a period of 10 years: data from the randomized CML-study IV. Leukemia 29, 1123-1132 (2015).
Second-generation tyrosine kinase inhibitors: The future of frontline CML therapy
Kantarjian, H. M., Baccarani, M., Jabbour, E., Saglio, G. & Cortes, J. E. Second-generation tyrosine kinase inhibitors: the future of frontline CML therapy. Clin. Cancer Res. 17, 1674-1683 (2011).
Discontinuation of imatinib in patients with chronic myeloid leukaemia who have maintained complete molecular remission for at least 2 years: The prospective, multicentre Stop Imatinib (STIM) trial
Mahon, F. X. et al. Discontinuation of imatinib in patients with chronic myeloid leukaemia who have maintained complete molecular remission for at least 2 years: the prospective, multicentre Stop Imatinib (STIM) trial. Lancet Oncol. 11, 1029-1035 (2010).
Safety and efficacy of imatinib cessation for CML patients with stable undetectable minimal residual disease: Results from the TWISTER study
Ross, D. M. et al. Safety and efficacy of imatinib cessation for CML patients with stable undetectable minimal residual disease: results from the TWISTER study. Blood 122, 515-522 (2013).
Binding or bending: Distinction of allosteric Abl kinase agonists from antagonists by an NMR-based conformational assay
Jahnke, W. et al. Binding or bending: distinction of allosteric Abl kinase agonists from antagonists by an NMR-based conformational assay. J. Am. Chem. Soc. 132, 7043-7048 (2010).
ABL001, a potent, allosteric inhibitor of BCR-ABL, exhibits safety and promising single-agent activity in a phase i study of patients with CML with failure of prior TKI therapy
Ottmann, O. G. et al. ABL001, a potent, allosteric inhibitor of BCR-ABL, exhibits safety and promising single-agent activity in a phase I study of patients with CML with failure of prior TKI therapy. Blood 126, 138 (2015).
Current event-free survival after sequential tyrosine kinase inhibitor therapy for chronic myeloid leukemia
Al-Kali, A. et al. Current event-free survival after sequential tyrosine kinase inhibitor therapy for chronic myeloid leukemia. Cancer 117, 327-335 (2011).
Assessment of BCR-ABL1 transcript levels at 3 months is the only requirement for predicting outcome for patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors
Marin, D. et al. Assessment of BCR-ABL1 transcript levels at 3 months is the only requirement for predicting outcome for patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors. J. Clin. Oncol. 30, 232-238 (2012).
Prognosis for patients with CML and > 10% BCR-ABL1 after 3 months of imatinib depends on the rate of BCR-ABL1 decline
Branford, S. et al. Prognosis for patients with CML and > 10% BCR-ABL1 after 3 months of imatinib depends on the rate of BCR-ABL1 decline. Blood 124, 511-518 (2014).
Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML)
Hanfstein, B. et al. Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML). Leukemia 26, 2096-2102 (2012).