ABL Kinase Gene Mutation Analysis and Gleevec® Resistance FeaturedTest Code ABL G Test Synonyms ABL kinase domain gene sequencing Associations Chronic myelogenous leukemia (CML), Acute lymphoblastic leukemia (ALL), Allogeneic bone marrow transplantation, Minimal residual disease (MRD), Molecular remission, Gleevec® resistance Methodology Quantitative reverse transcriptase PCR (RT-PCR), Semi-nested PCR, Bi-directional DNA sequencing CPT Codes 83891 x3 – Isolation or extraction of highly purified nucleic acid 83892 x1 – Enzymatic digestion 83902 x1 – Reverse transcription 83898 x3 – Amplification of patient nucleic acid, single primer pair, each primer pair 83894 x1 – Separation by gel electrophoresis 83904 x5 – Mutation identification by sequencing, single segment, each segment 83912-26 – Interpretation and report Turnaround Time 10 days Specimen Requirements
Specimen Stability
Storage & Handling Causes for Rejection Specimen >48 hours old; Specimen clotted; Stored or shipped at incorrect temperature; Incorrect anticoagulant; Insufficient specimen volume Reference Range ABL Kinase domain mutation(s) detected and characterized / not detected Related Content BCR/ABL major and minor by quantitative PCR for MRD
Description Screening of CML patients who (1) fail to achieve a complete hematologic response at 3 months (2) have no cytogenetic response at 6 months (3) fail to achieve a major cytogenetic response at 12 months, or (4) any loss of response (hematologic, cytogenetic or molecular). References
Trademarks Gleevec® is a registered trademark of the Novartis Pharmaceuticals Corporation. |