Molecular Pathology Laboratory Network

BCR/ABL Quantitative PCR major and /or minor

Test Code
P BCR ABL
Test Synonyms
Philadelphia Chromosome; major t(9;22) e13/e14(p210), minor t(9;22) e1 (p190)
Associations
Chronic myelogenous leukemia (CML), Acute lymphoblastic leukemia (ALL), Allogeneic bone marrow transplantation, Minimal residual disease (MRD), Molecular remission
Methodology
Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) for BCR/ABL major t(9;22) e13/e14(p210) and minor t(9;22) e1 (p190) fusion gene transcipts.
CPT Codes
Please contact a client service specialist at 800.932.2943
Turnaround Time
3-5 days
Specimen Requirements
  • 10.0 mL (min. 9.0 mL) peripheral blood in EDTA
  • 5.0 mL (min. 2.5 mL) bone marrow in EDTA
Specimen Stability
  • Specimen must be received by MPLN within 48 hours of collection
  • Stable at 2-8°C
Storage & Handling
  • Ship peripheral blood and bone marrow at ambient temperature (Do not ship on ice or cold pack)
  • Please notify us if shipment is to arrive after 1 p.m. Friday or Saturday
  • Causes for Rejection
    Specimen >48 hours old; Specimen clotted; Specimen stored or shipped at incorrect temperature; Specimen in incorrect anticoagulant; Insufficient specimen volume
    Reference Range
    Positive: major or minor BCR/ABL fusion quantified relative to ABL
    Negative: major or minor BCR/ABL fusion not detected, less than 0.001% BCR/ABL
    Related Content
    Cytogenetics
    Flow Cytometry
    BCR/ABL by FISH
    BCR/ABL disease monitoring by quantitative PCR
    ABL kinase gene mutation for Gleevec resistance
    Description
    Molecular detection of the BCR/ABL fusion gene transcript (e13a2, e14a2, e1a2) in patients with a Philadelphia (t[(9;22)(q34;q11.2)]) positive leukemia. The translocation is found in >99% of CML patients, ~20% of adult acute lymphoblastic leukemia (ALL), ~5% of pediatric ALL, and ~2% of acute myeloid leukemia (AML).

    The primary clinical utilities for BCR/ABL quantitative PCR testing include (1) identfication of fusion gene transcript and determination of baseline level of BCR-ABL expression in newly diagnosed CML patients, and (2) the monitoring of patients for molecular evidence of minimal residual disease (MRD) or molecular remission in response to tyrosine kinase inhibitor (TKI) therapy or allogeneic stem cell transplantation.
    References
    Jabbour E et al. (2008). Molecular monitoring in chronic myeloid leukemia. Cancer. 112:2112-2118.
    Trademarks
    Gleevec® is a registered trademark of the Novartis Pharmaceuticals Corporation.

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