Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

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,

. 2016 ; 17 (5) : . [pub] 20160429

Language English Country Switzerland

Document type Comparative Study, Journal Article

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.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17013894
003      
CZ-PrNML
005      
20170418105301.0
007      
ta
008      
170413s2016 sz f 000 0|eng||
009      
AR
024    7_
$a 10.3390/ijms17050642 $2 doi
035    __
$a (PubMed)27136541
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Preuner, Sandra $u Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, A-1090 Vienna, Austria. sandra.preuner@ccri.at.
245    10
$a Quantitative Analysis of Mutant Subclones in Chronic Myeloid Leukemia: Comparison of Different Methodological Approaches / $c S. Preuner, A. Barna, F. Frommlet, S. Czurda, B. Konstantin, M. Alikian, K. Machova Polakova, T. Sacha, J. Richter, T. Lion, C. Gabriel,
520    9_
$a 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.
650    _2
$a srovnávací genomová hybridizace $7 D055028
650    _2
$a DNA $x analýza $x genetika $x metabolismus $7 D004247
650    _2
$a bcr-abl fúzní proteiny $x chemie $x genetika $7 D016044
650    12
$a vysoce účinné nukleotidové sekvenování $7 D059014
650    _2
$a lidé $7 D006801
650    _2
$a chronická myeloidní leukemie $x genetika $x patologie $7 D015464
650    12
$a polymerázová řetězová reakce $7 D016133
650    12
$a sekvenční analýza DNA $7 D017422
655    _2
$a srovnávací studie $7 D003160
655    _2
$a časopisecké články $7 D016428
700    1_
$a Barna, Agnes $u Red Cross Transfusion Service for Upper Austria, A-4017 Linz, Austria. agnes.barna@o.roteskreuz.at.
700    1_
$a Frommlet, Florian $u Department for Medical Statistics, Medical University of Vienna, A-1090 Vienna, Austria. florian.frommlet@meduniwien.ac.at.
700    1_
$a Czurda, Stefan $u Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, A-1090 Vienna, Austria. stefan.czurda@ccri.at.
700    1_
$a Konstantin, Byrgazov $u Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, A-1090 Vienna, Austria. konstantin.byrgazov@ccri.at.
700    1_
$a Alikian, Mary $u Imperial Molecular Pathology Laboratory, Hammersmith Hospital, Imperial College Healthcare National Health Service (NHS) Trust, London W12 0HS, UK. m.alikian@imperial.ac.uk. $7 gn_A_00004260
700    1_
$a Machova Polakova, Katerina $u Institute of Hematology and Blood Transfusion, 128 20 Prague, Czech Republic. katerina.machova@lf1.cuni.cz.
700    1_
$a Sacha, Tomasz $u Hematology Department, Jagiellonian University, 31-501 Krakow, Poland. sachatom@gmail.com.
700    1_
$a Richter, Johan $u Section for Hematology, Department of Medicine, University Hospital of Lund, 221 00 Lund, Sweden. johan.richter@med.lu.se.
700    1_
$a Lion, Thomas $u Children's Cancer Research Institute (CCRI), Zimmermannplatz 10, A-1090 Vienna, Austria. thomas.lion@ccri.at. Department of Pediatrics, Medical University Vienna, A-1090 Vienna, Austria. thomas.lion@ccri.at.
700    1_
$a Gabriel, Christian $u Red Cross Transfusion Service for Upper Austria, A-4017 Linz, Austria. christian.gabriel@o.roteskreuz.at.
773    0_
$w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 17, č. 5 (2016)
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27136541 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20170413 $b ABA008
991    __
$a 20170418105609 $b ABA008
999    __
$a ok $b bmc $g 1200359 $s 974672
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2016 $b 17 $c 5 $e 20160429 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
LZP    __
$a Pubmed-20170413

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...