Back to Search
Start Over
Chronic Myeloid Leukemia - Prognostic Value of Mutations
- Source :
- Asian Pacific Journal of Cancer Prevention. 16:7415-7423
- Publication Year :
- 2015
- Publisher :
- Asian Pacific Organization for Cancer Prevention, 2015.
-
Abstract
- Chronic myeloid leukemia (CML) is a stem cell disorder characterized by unrestricted proliferation of the myeloid series that occurs due to the BCR-ABL fusion oncogene as a result of reciprocal translocation t(9;22) (q34;q11). This discovery has made this particular domain a target for future efforts to cure CML. Imatinib revolutionized the treatment options for CML and gave encouraging results both in case of safety as well as tolerability profile as compared to agents such as hydroxyurea or busulfan given before Imatinib. However, about 2-4% of patients show resistance and mutations have been found to be one of the reasons for its development. European Leukemianet gives recommendations for BCR-ABL mutational analysis along with other tyrosine kinase inhibitors (TKIs) that should be administered according to the mutations harbored in a patient. The following overview gives recommendations for monitoring patients on the basis of their mutational status.
- Subjects :
- Cancer Research
Myeloid
Epidemiology
DNA Mutational Analysis
Fusion Proteins, bcr-abl
Antineoplastic Agents
European LeukemiaNet
Myelogenous
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
hemic and lymphatic diseases
medicine
Humans
Protein Kinase Inhibitors
neoplasms
ABL
business.industry
Public Health, Environmental and Occupational Health
Myeloid leukemia
Imatinib
Prognosis
medicine.disease
Leukemia
medicine.anatomical_structure
Imatinib mesylate
Oncology
Drug Resistance, Neoplasm
Mutation
Imatinib Mesylate
Cancer research
business
medicine.drug
Subjects
Details
- ISSN :
- 15137368
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Asian Pacific Journal of Cancer Prevention
- Accession number :
- edsair.doi.dedup.....55f6a52ab90dbcf59b9571b3d814e553
- Full Text :
- https://doi.org/10.7314/apjcp.2015.16.17.7415