Abstract
BCR-ABL1 kinase domain mutations were evaluated in 60 imatinib-resistant patients with Philadelphia-positive (Ph(+)) leukemia using PCR-Invader assay and direct sequencing. In chronic myelogenous leukemia (CML)--chronic phase (CP), 5 had P-loop mutations and 3 had T315I mutations. CML-CP patients with high Sokal score showed significantly higher incidence of mutations. P-loop mutations were associated with higher risk of disease progression. In CML-advanced phase, P-loop mutations and T315I mutation were associated with significantly shorter survival. In Ph(+) acute lymphoblastic leukemia, overall survival was poor irrespective of mutational status. The PCR-Invader assay is useful for screening of mutations and prediction of prognosis.
Copyright © 2010 Elsevier Ltd. All rights reserved.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Aged, 80 and over
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Antineoplastic Agents / therapeutic use
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Benzamides
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DNA Mutational Analysis / methods
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Drug Resistance, Neoplasm / genetics*
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Female
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Fusion Proteins, bcr-abl / analysis
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Fusion Proteins, bcr-abl / chemistry
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Fusion Proteins, bcr-abl / genetics*
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Genetic Testing / methods
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Humans
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Imatinib Mesylate
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / diagnosis
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
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Male
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Middle Aged
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Mutation* / physiology
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Phosphotransferases / chemistry
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Phosphotransferases / genetics
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Piperazines / therapeutic use*
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Polymerase Chain Reaction / methods*
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Prognosis
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Protein Structure, Tertiary / genetics
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Pyrimidines / therapeutic use*
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Survival Analysis
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Young Adult
Substances
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Antineoplastic Agents
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Benzamides
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Piperazines
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Pyrimidines
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Imatinib Mesylate
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Phosphotransferases
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Fusion Proteins, bcr-abl