Abstract
Tyrosine kinase inhibitor (TKI) therapy targeting the BCR-ABL1 kinase is effective against chronic myeloid leukaemia (CML), but is not curative for most patients. Minimal residual disease (MRD) is thought to reside in TKI-insensitive leukaemia stem cells (LSCs) that are not fully addicted to BCR-ABL1. Recent conceptual advances in both CML biology and therapeutic intervention have increased the potential for the elimination of CML cells, including LSCs, through simultaneous inhibition of BCR-ABL1 and other newly identified, crucial targets.
Trial registration:
ClinicalTrials.gov NCT00574873 NCT00827138 NCT01207440.
MeSH terms
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Animals
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Fusion Proteins, bcr-abl / antagonists & inhibitors*
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Fusion Proteins, bcr-abl / metabolism
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Humans
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / enzymology
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Molecular Targeted Therapy / methods
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Protein Kinase Inhibitors / pharmacology*
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Protein Kinase Inhibitors / therapeutic use*
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Protein-Tyrosine Kinases / antagonists & inhibitors*
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Protein-Tyrosine Kinases / metabolism
Substances
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Protein Kinase Inhibitors
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Protein-Tyrosine Kinases
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Fusion Proteins, bcr-abl
Associated data
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ClinicalTrials.gov/NCT00574873
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ClinicalTrials.gov/NCT00827138
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ClinicalTrials.gov/NCT01207440