BCR-ABL Quantitative (Philadelphia Chromosome) is a highly specialized molecular hematology test used to detect and quantify BCR-ABL1 fusion gene transcripts caused by the t(9;22) translocation, also known as the Philadelphia chromosome. This test is primarily used for the diagnosis support, baseline quantification, treatment monitoring, molecular response assessment, and relapse surveillance of Chronic Myeloid Leukemia (CML) and selected cases of Philadelphia chromosome-positive Acute Lymphoblastic Leukemia (Ph+ ALL). The assay is commonly performed using Quantitative Reverse Transcription PCR (RT-PCR / qRT-PCR) to measure BCR-ABL1 mRNA transcript levels, most commonly the p210 (major breakpoint; e13a2/e14a2) transcript associated with CML, and in some panels also the p190 (minor breakpoint; e1a2) transcript associated more often with Ph+ ALL. For p210 BCR-ABL1, results are often standardized to the International Scale (IS) and reported as % BCR-ABL1/ABL1, enabling long-term treatment monitoring and response comparison across time. This test is essential for evaluating response to tyrosine kinase inhibitor (TKI) therapy such as imatinib, dasatinib, nilotinib, bosutinib, or ponatinib, and helps guide hematology/oncology treatment decisions. Labcorp notes that the assay can detect e13a2 (b2a2), e14a2 (b3a2), and e1a2 (p190) transcripts, and for p210 the numeric result is reported as % BCR-ABL1/ABL1 on the International Scale (IS).
Fasting
Not Required
Reporting Time
7–10 Days
Gender
Male/Female
Age Group
5-99 yrs.
✔ Home collection available ✔ No hidden charges
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