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Sequential development of mutant clones in an imatinib resistant chronic myeloid leukaemia patient following sequential treatment with multiple tyrosine kinase inhibitors: an emerging problem?
- Publication Year :
- 2009
-
Abstract
- With the increasing use of new tyrosine kinase inhibitors it has been suggested that the spectrum of kinase domain mutations may change and possible selection of new resistant clones may occur. We describe a Ph + chronic myeloid leukaemia (CML) patient with primary resistance to imatinib who received without success sequential therapy with multiple TKIs, and developed sequential emergence of kinase domain mutations after these treatments.
- Subjects :
- Cancer Research
medicine.drug_class
Mutant
Antineoplastic Agents
Biology
Toxicology
medicine.disease_cause
Tyrosine-kinase inhibitor
Piperazines
Chronic myeloid leukaemia - Resistance - Tyrosine kinase inhibitors - Mutations
BCR-ABL MUTATIONS
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
hemic and lymphatic diseases
medicine
Humans
Pharmacology (medical)
Protein Kinase Inhibitors
Pharmacology
Mutation
Cancer
Imatinib
Middle Aged
Protein-Tyrosine Kinases
medicine.disease
DOMAIN MUTATIONS
Pyrimidines
Oncology
Protein kinase domain
BMS-354825
Drug Resistance, Neoplasm
Benzamides
Cancer research
Imatinib Mesylate
Female
AMN107
Tyrosine kinase
CHRONIC MYELOID LEUKEMIA (CML)
Chronic myelogenous leukemia
medicine.drug
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....d75077795b1911b7d3f0d046ce685e81