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Quantitative Analysis of Mutant Subclones in Chronic Myeloid Leukemia: Comparison of Different Methodological Approaches
S. Preuner, A. Barna, F. Frommlet, S. Czurda, B. Konstantin, M. Alikian, K. Machova Polakova, T. Sacha, J. Richter, T. Lion, C. Gabriel,
Language English Country Switzerland
Document type Comparative Study, Journal Article
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
27136541
DOI
10.3390/ijms17050642
Knihovny.cz E-resources
- MeSH
- Fusion Proteins, bcr-abl chemistry genetics MeSH
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive genetics pathology MeSH
- DNA analysis genetics metabolism MeSH
- Humans MeSH
- Polymerase Chain Reaction * MeSH
- Sequence Analysis, DNA * MeSH
- Comparative Genomic Hybridization MeSH
- High-Throughput Nucleotide Sequencing * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
Identification and quantitative monitoring of mutant BCR-ABL1 subclones displaying resistance to tyrosine kinase inhibitors (TKIs) have become important tasks in patients with Ph-positive leukemias. Different technologies have been established for patient screening. Various next-generation sequencing (NGS) platforms facilitating sensitive detection and quantitative monitoring of mutations in the ABL1-kinase domain (KD) have been introduced recently, and are expected to become the preferred technology in the future. However, broad clinical implementation of NGS methods has been hampered by the limited accessibility at different centers and the current costs of analysis which may not be regarded as readily affordable for routine diagnostic monitoring. It is therefore of interest to determine whether NGS platforms can be adequately substituted by other methodological approaches. We have tested three different techniques including pyrosequencing, LD (ligation-dependent)-PCR and NGS in a series of peripheral blood specimens from chronic myeloid leukemia (CML) patients carrying single or multiple mutations in the BCR-ABL1 KD. The proliferation kinetics of mutant subclones in serial specimens obtained during the course of TKI-treatment revealed similar profiles via all technical approaches, but individual specimens showed statistically significant differences between NGS and the other methods tested. The observations indicate that different approaches to detection and quantification of mutant subclones may be applicable for the monitoring of clonal kinetics, but careful calibration of each method is required for accurate size assessment of mutant subclones at individual time points.
Children's Cancer Research Institute Zimmermannplatz 10 A 1090 Vienna Austria
Department for Medical Statistics Medical University of Vienna A 1090 Vienna Austria
Hematology Department Jagiellonian University 31 501 Krakow Poland
Institute of Hematology and Blood Transfusion 128 20 Prague Czech Republic
Red Cross Transfusion Service for Upper Austria A 4017 Linz Austria
Section for Hematology Department of Medicine University Hospital of Lund 221 00 Lund Sweden
References provided by Crossref.org
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