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Erschienen in: Journal of Cancer Research and Clinical Oncology 5/2015

01.05.2015 | Original Article - Clinical Oncology

Next-generation deep sequencing improves detection of BCR-ABL1 kinase domain mutations emerging under tyrosine kinase inhibitor treatment of chronic myeloid leukemia patients in chronic phase

verfasst von: Katerina Machova Polakova, Vojtech Kulvait, Adela Benesova, Jana Linhartova, Hana Klamova, Monika Jaruskova, Caterina de Benedittis, Torsten Haferlach, Michele Baccarani, Giovanni Martinelli, Tomas Stopka, Thomas Ernst, Andreas Hochhaus, Alexander Kohlmann, Simona Soverini

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 5/2015

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Abstract

Purpose

Here, we studied whether amplicon next-generation deep sequencing (NGS) could improve the detection of emerging BCR-ABL1 kinase domain mutations in chronic phase chronic myeloid leukemia (CML) patients under tyrosine kinase inhibitor (TKI) treatment and discussed the clinical relevance of such sensitive mutational detection.

Methods

For NGS data evaluation including extraction of biologically relevant low-level variants from background error noise, we established and applied a robust and versatile bioinformatics approach.

Results

Results from a retrospective longitudinal analysis of 135 samples of 15 CML patients showed that NGS could have revealed emerging resistant mutants 2–11 months earlier than conventional sequencing. Interestingly, in cases who later failed first-line imatinib treatment, NGS revealed that TKI-resistant mutations were already detectable at the time of major or deeper molecular response. Identification of emerging mutations by NGS was mirrored by BCR-ABL1 transcript level expressed either fluctuations around 0.1 %IS or by slight transcript level increase. NGS also allowed tracing mutations that emerged during second-line TKI therapy back to the time of switchover. Compound mutants could be detected in three cases, but were not found to outcompete single mutants.

Conclusions

This work points out, that next-generation deep sequencing, coupled with a robust bioinformatics approach for mutation calling, may be just in place to ensure reliable detection of emerging BCR-ABL1 mutations, allowing early therapy switch and selection of the most appropriate therapy. Further, prospective assessment of how to best integrate NGS in the molecular monitoring and clinical decision algorithms is warranted.
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Metadaten
Titel
Next-generation deep sequencing improves detection of BCR-ABL1 kinase domain mutations emerging under tyrosine kinase inhibitor treatment of chronic myeloid leukemia patients in chronic phase
verfasst von
Katerina Machova Polakova
Vojtech Kulvait
Adela Benesova
Jana Linhartova
Hana Klamova
Monika Jaruskova
Caterina de Benedittis
Torsten Haferlach
Michele Baccarani
Giovanni Martinelli
Tomas Stopka
Thomas Ernst
Andreas Hochhaus
Alexander Kohlmann
Simona Soverini
Publikationsdatum
01.05.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 5/2015
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-014-1845-6

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