Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia
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COMMENTARY
Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia Elia Mattarucchi1 • Francesco Pallotti2,3 • Rosario Casalone2
Ó Springer International Publishing Switzerland 2015
Clinical papers frequently lack in-depth descriptions of analytical methods, triggering possible doubts regarding their conclusions. Through this short communication, we would like to stimulate a debate on the monitoring of chronic myeloid leukemia, a disorder that requires frequent laboratory analysis by RNA reverse transcription and realtime quantitative PCR (RQ-PCR). This is a challenging procedure influenced by a number of factors that are difficult to control [1, 2], and troubled by the need to use reference materials to standardize results against the socalled international scale (IS) [3]. The residual disease is evaluated through the amount of BCR-ABL1 transcript, and a patient’s response is reported in terms of IS logarithmic reductions, up to the possible condition of apparent undetectable disease [2]. Actually, the outcome of RQ-PCR represents only an estimation of the leukemic clone based on the assumed proportionality between chimeric RNA and leukemic cells. However, it is not clear if this proportionality is still valid at very high response levels, and negative results can be interpreted in a number of ways, e.g., the true absence of leukemic cells, the presence of leukemic cells that do not transcribe chimeric RNA [4], or measurements below the detection limit. Really, an accurate determination of the detection limit is not feasible since specimen
& Elia Mattarucchi [email protected] 1
Department of Experimental and Clinical Medicine, Universita` dell’Insubria, via Dunant 5, 21100 Varese, Italy
2
Medical Genetics Unit, Ospedale di Circolo e Fondazione Macchi, Varese, Italy
3
Department of Surgical and Morphological Science, Universita` dell’Insubria, Varese, Italy
handling, RNA extraction and retro-transcription are critical pre-analytical steps (due to in vitro RNA instability), and it is practically impossible to characterize the whole process. Even positive (but barely detectable) results are difficult to interpret because of the intrinsic variability of gene expression: patients with few leukemic cells can give significantly different results, depending on small variations in the mutual transcription levels of BCR-ABL1 and the reference gene used as a normalizer (usually ABL1, BCR, or GUSB [1]). As a consequence, a clear definition of molecular response is still under elaboration, though the potential for drug discontinuation makes this subject a pressing issue [2]. A survey conducted by the College of American Pathologists pointed out that diverse laboratories testing the same sample obtained different results [1]. Pilot methods based on DNA analysis have also been introduced. These methods require the sequence of the BCR-ABL1 junction for each patient, but have the advantage, of relying on a direct and univocal relationship between cell number and breakpoints (i.e., similar to cyto
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