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Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC

In non-small cell lung cancer (NSCLC) the usage of plasma-derived circulating tumor DNA (ctDNA) have come into focus to obtain a comprehensive genetic profile of a given lung cancer. Despite the usage of specific sampling tubes, archived plasma samples as well as inappropriately treated blood sample...

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Autores principales: Mayer, Stefanie, Schmidtke-Schrezenmeier, Gerlinde, Buske, Christian, Rücker, Frank G., Barth, Thomas F.E., Möller, Peter, Marienfeld, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409026/
https://www.ncbi.nlm.nih.gov/pubmed/32708545
http://dx.doi.org/10.3390/cancers12071917
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author Mayer, Stefanie
Schmidtke-Schrezenmeier, Gerlinde
Buske, Christian
Rücker, Frank G.
Barth, Thomas F.E.
Möller, Peter
Marienfeld, Ralf
author_facet Mayer, Stefanie
Schmidtke-Schrezenmeier, Gerlinde
Buske, Christian
Rücker, Frank G.
Barth, Thomas F.E.
Möller, Peter
Marienfeld, Ralf
author_sort Mayer, Stefanie
collection PubMed
description In non-small cell lung cancer (NSCLC) the usage of plasma-derived circulating tumor DNA (ctDNA) have come into focus to obtain a comprehensive genetic profile of a given lung cancer. Despite the usage of specific sampling tubes, archived plasma samples as well as inappropriately treated blood samples still cause a loss of information due to cell lysis and contamination with cellular DNA. Our aim was to establish a reliable protocol to rescue ctDNA from such non-informative samples to monitor the mutational landscape in NSCLC. As a proof-of-concept study we used archived plasma samples derived from whole blood EDTA samples of 51 patients suffering from NSCLC. Analysis of the isolated plasma DNA determined only a small fraction of ctDNA in a range of 90–250 bp. By applying a specific purification procedure, we were able to increase the informative ctDNA content and improve in a cohort of 42 patients the detection of driver mutations from 32% to 79% of the mutations found in tissue biopsies. Thus, we present here an easy to perform, time and cost effective procedure to rescue non-informative ctDNA samples, which is sufficient to detect oncogenic mutations in NGS approaches and is therefore a valuable technical improvement for laboratories handling liquid biopsy samples.
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spelling pubmed-74090262020-08-26 Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC Mayer, Stefanie Schmidtke-Schrezenmeier, Gerlinde Buske, Christian Rücker, Frank G. Barth, Thomas F.E. Möller, Peter Marienfeld, Ralf Cancers (Basel) Article In non-small cell lung cancer (NSCLC) the usage of plasma-derived circulating tumor DNA (ctDNA) have come into focus to obtain a comprehensive genetic profile of a given lung cancer. Despite the usage of specific sampling tubes, archived plasma samples as well as inappropriately treated blood samples still cause a loss of information due to cell lysis and contamination with cellular DNA. Our aim was to establish a reliable protocol to rescue ctDNA from such non-informative samples to monitor the mutational landscape in NSCLC. As a proof-of-concept study we used archived plasma samples derived from whole blood EDTA samples of 51 patients suffering from NSCLC. Analysis of the isolated plasma DNA determined only a small fraction of ctDNA in a range of 90–250 bp. By applying a specific purification procedure, we were able to increase the informative ctDNA content and improve in a cohort of 42 patients the detection of driver mutations from 32% to 79% of the mutations found in tissue biopsies. Thus, we present here an easy to perform, time and cost effective procedure to rescue non-informative ctDNA samples, which is sufficient to detect oncogenic mutations in NGS approaches and is therefore a valuable technical improvement for laboratories handling liquid biopsy samples. MDPI 2020-07-16 /pmc/articles/PMC7409026/ /pubmed/32708545 http://dx.doi.org/10.3390/cancers12071917 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mayer, Stefanie
Schmidtke-Schrezenmeier, Gerlinde
Buske, Christian
Rücker, Frank G.
Barth, Thomas F.E.
Möller, Peter
Marienfeld, Ralf
Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC
title Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC
title_full Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC
title_fullStr Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC
title_full_unstemmed Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC
title_short Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC
title_sort rescue of non-informative circulating tumor dna to monitor the mutational landscape in nsclc
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409026/
https://www.ncbi.nlm.nih.gov/pubmed/32708545
http://dx.doi.org/10.3390/cancers12071917
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