Table I.
Method | Target | Sensitivity | Advantages | Disadvantages |
---|---|---|---|---|
Conventional Cytogenetics | Chromosomal translocation = t(9;22) | 10%-5% | The gold standard, and detection of other large chromosomal changes. | Require dividing cells and highly skilled technician. Very labor and time intensive. Miss cryptic translocations. |
Fluorescence in situ hybridization (FISH) | BCR-ABL1 DNA | 0.1%-5% | Can use wider range of specimens (PB, BM, FFPE). Can detect cryptic translocations. | Relatively insensitive compared with qRT-PCR. Requires skilled technicians. Highly specific to targeted region and will miss other chromosomal changes. |
Quantitative reverse transcription polymerase chain reaction (qRT-PCR) | BCR-ABL1 mRNA | 0.001%-0.01% | Very sensitive. Can use wider range of specimens (PB, BM, FFPE). Can detect cryptic translocations. | Not well standardized across laboratories. More suceptable to contamination or RNA degradation issues. |
CML = chronic myelogenous leukemia, PB = peripheral blood, BM = bone marrow, FFPE = formalin fixed parraffin embedded tissue