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

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  • Steffen Grann Jensen
  • Samantha Epistolio
  • Cesilie Lind Madsen
  • Majbritt Hauge Kyneb
  • Alice Riva
  • Alessia Paganotti
  • Jessica Barizzi
  • Rasmus Koefoed Petersen
  • Michael Børgesen
  • Francesca Molinari
  • Renzo Boldorini
  • Jan Lorenzen
  • Erik Sørensen
  • Ulf Bech Christensen
  • Høgdall, Estrid Vilma Solyom
  • Milo Frattini

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 R20,97 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.

OriginalsprogEngelsk
Artikelnummere0253687
TidsskriftPlos One
Vol/bind16
Udgave nummer6 June
Sider (fra-til)1-21
ISSN1932-6203
DOI
StatusUdgivet - 2021

Bibliografisk note

Publisher Copyright:
Copyright: © 2021 Jensen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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