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A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies

BACKGROUND: A major perspective for the use of circulating tumor DNA (ctDNA) in the clinical setting of non-small cell lung cancer (NSCLC) is expected as predictive factor for resistance and response to EGFR TKI therapy and, especially, as a non-invasive alternative to tissue biopsy. However, ctDNA...

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Autores principales: Jensen, Steffen Grann, Epistolio, Samantha, Madsen, Cesilie Lind, Kyneb, Majbritt Hauge, Riva, Alice, Paganotti, Alessia, Barizzi, Jessica, Petersen, Rasmus Koefoed, Børgesen, Michael, Molinari, Francesca, Boldorini, Renzo, Lorenzen, Jan, Sørensen, Erik, Christensen, Ulf Bech, Høgdall, Estrid, Frattini, Milo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224962/
https://www.ncbi.nlm.nih.gov/pubmed/34166445
http://dx.doi.org/10.1371/journal.pone.0253687
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author Jensen, Steffen Grann
Epistolio, Samantha
Madsen, Cesilie Lind
Kyneb, Majbritt Hauge
Riva, Alice
Paganotti, Alessia
Barizzi, Jessica
Petersen, Rasmus Koefoed
Børgesen, Michael
Molinari, Francesca
Boldorini, Renzo
Lorenzen, Jan
Sørensen, Erik
Christensen, Ulf Bech
Høgdall, Estrid
Frattini, Milo
author_facet Jensen, Steffen Grann
Epistolio, Samantha
Madsen, Cesilie Lind
Kyneb, Majbritt Hauge
Riva, Alice
Paganotti, Alessia
Barizzi, Jessica
Petersen, Rasmus Koefoed
Børgesen, Michael
Molinari, Francesca
Boldorini, Renzo
Lorenzen, Jan
Sørensen, Erik
Christensen, Ulf Bech
Høgdall, Estrid
Frattini, Milo
author_sort Jensen, Steffen Grann
collection PubMed
description BACKGROUND: A major perspective for the use of circulating tumor DNA (ctDNA) in the clinical setting of non-small cell lung cancer (NSCLC) is expected as predictive factor for resistance and response to EGFR TKI therapy and, especially, as a non-invasive alternative to tissue biopsy. However, ctDNA is both highly fragmented and mostly low concentrated in plasma and serum. On this basis, it is important to use a platform characterized by high sensitivity and linear performance in the low concentration range. This motivated us to evaluate the newly developed and commercially available SensiScreen(®) EGFR Liquid assay platform (PentaBase) with regard to sensitivity, linearity, repeatability and accuracy and finally to compare it to our already implemented methods. The validation was made in three independent European laboratories using two cohorts on a total of 68 unique liquid biopsies. RESULTS: Using artificial samples containing 1600 copies of WT DNA spiked with 50% - 0.1% of mutant copies across a seven—log dilution scale, we assessed the sensitivity, linearity, repeatability and accuracy for the p.T790M, p.L858R and exon 19 deletion assays of the SensiScreen(®) EGFR Liquid assay platform. The lowest value detectable ranged from 0.5% to 0.1% with R(2)≥0,97 indicating good linearity. High PCR efficiency was shown for all three assays. In 102 single PCRs each containing theoretical one copy of the mutant at initiating, assays showed repeatable positivity in 75.5% - 80.4% of reactions. At low ctDNA levels, as in plasma, the SensiScreen(®) EGFR Liquid assay platform showed better sensitivity than the Therascreen(®) EGFR platform (Qiagen) and equal performance to the ctEGFR Mutation Detection Kit (EntroGen) and the IOT(®) Oncomine cell-free nucleic acids assay (Thermo Fisher Scientific) with 100% concordance at the sequence level. CONCLUSION: For profiling clinical plasma samples, characterized by low ctDNA abundance, the SensiScreen(®) EGFR Liquid assay is able to identify down to 1 copy of mutant alleles and with its high sensitivity, linearity and accuracy it may be a competitive platform of choice.
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spelling pubmed-82249622021-07-19 A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies Jensen, Steffen Grann Epistolio, Samantha Madsen, Cesilie Lind Kyneb, Majbritt Hauge Riva, Alice Paganotti, Alessia Barizzi, Jessica Petersen, Rasmus Koefoed Børgesen, Michael Molinari, Francesca Boldorini, Renzo Lorenzen, Jan Sørensen, Erik Christensen, Ulf Bech Høgdall, Estrid Frattini, Milo PLoS One Research Article BACKGROUND: A major perspective for the use of circulating tumor DNA (ctDNA) in the clinical setting of non-small cell lung cancer (NSCLC) is expected as predictive factor for resistance and response to EGFR TKI therapy and, especially, as a non-invasive alternative to tissue biopsy. However, ctDNA is both highly fragmented and mostly low concentrated in plasma and serum. On this basis, it is important to use a platform characterized by high sensitivity and linear performance in the low concentration range. This motivated us to evaluate the newly developed and commercially available SensiScreen(®) EGFR Liquid assay platform (PentaBase) with regard to sensitivity, linearity, repeatability and accuracy and finally to compare it to our already implemented methods. The validation was made in three independent European laboratories using two cohorts on a total of 68 unique liquid biopsies. RESULTS: Using artificial samples containing 1600 copies of WT DNA spiked with 50% - 0.1% of mutant copies across a seven—log dilution scale, we assessed the sensitivity, linearity, repeatability and accuracy for the p.T790M, p.L858R and exon 19 deletion assays of the SensiScreen(®) EGFR Liquid assay platform. The lowest value detectable ranged from 0.5% to 0.1% with R(2)≥0,97 indicating good linearity. High PCR efficiency was shown for all three assays. In 102 single PCRs each containing theoretical one copy of the mutant at initiating, assays showed repeatable positivity in 75.5% - 80.4% of reactions. At low ctDNA levels, as in plasma, the SensiScreen(®) EGFR Liquid assay platform showed better sensitivity than the Therascreen(®) EGFR platform (Qiagen) and equal performance to the ctEGFR Mutation Detection Kit (EntroGen) and the IOT(®) Oncomine cell-free nucleic acids assay (Thermo Fisher Scientific) with 100% concordance at the sequence level. CONCLUSION: For profiling clinical plasma samples, characterized by low ctDNA abundance, the SensiScreen(®) EGFR Liquid assay is able to identify down to 1 copy of mutant alleles and with its high sensitivity, linearity and accuracy it may be a competitive platform of choice. Public Library of Science 2021-06-24 /pmc/articles/PMC8224962/ /pubmed/34166445 http://dx.doi.org/10.1371/journal.pone.0253687 Text en © 2021 Jensen et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jensen, Steffen Grann
Epistolio, Samantha
Madsen, Cesilie Lind
Kyneb, Majbritt Hauge
Riva, Alice
Paganotti, Alessia
Barizzi, Jessica
Petersen, Rasmus Koefoed
Børgesen, Michael
Molinari, Francesca
Boldorini, Renzo
Lorenzen, Jan
Sørensen, Erik
Christensen, Ulf Bech
Høgdall, Estrid
Frattini, Milo
A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies
title A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies
title_full A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies
title_fullStr A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies
title_full_unstemmed A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies
title_short A new sensitive and fast assay for the detection of EGFR mutations in liquid biopsies
title_sort new sensitive and fast assay for the detection of egfr mutations in liquid biopsies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224962/
https://www.ncbi.nlm.nih.gov/pubmed/34166445
http://dx.doi.org/10.1371/journal.pone.0253687
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