The major mechanism of imatinib resistance for patients with chronic myeloid leukemia (CML) is clonal expansion of leukemic cells with mutations in the Bcr-Abl fusion tyrosine kinase that reduce the capacity of imatinib to inhibit kinase activity. The early detection of such mutations may allow timely treatment intervention to prevent or overcome resistance. Direct sequencing of theBCR-ABLkinase domain is relatively rapid and allows detection of emerging mutations at a sensitivity of approx 20%. Mutations have been detected over a range of 242 amino acids, which spans the entire kinase domain. For optimal sensitivity, the kinase domain of the abnormal gene should be isolated by reverse-transcription (RT) polymerase chain reaction (PCR) amplification using primers that hybridize to theBCRandABLgenes. The quality of the RNA is assessed by real-time quantitative PCR prior to analysis, andBCR-ABLlevels are determined. Only RNA of adequate quality is used to ensure accurate and reproducible mutation analysis. Depending on the level ofBCR-ABLtranscripts, a one- or two-step PCR is required to amplify the kinase domain. Direct sequencing with dye terminator chemistry is performed using PCR-purified products. The sequence is compared to anABLkinase domain reference sequence using sequencing analysis software, which aligns the sequences and highlights single or multiple mutations.
