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Routine Molecular Screening of Patients with Advanced Non-SmallCell Lung Cancer in Circulating Cell-Free DNA at Diagnosis and During Progression Using OncoBEAMTM EGFR V2 and NGS Technologies.

Jessica GarciaArnaud GauthierGaëlle LescuyerDavid BarthelemyFlorence GeiguerJulie BalandierDaniel L EdelsteinFrederick S JonesFrank HoltrupMickael DuruisseauEmmanuel GrolleauClaire Rodriguez-LafrassePatrick MerleSébastien CouraudLéa Payen
Published in: Molecular diagnosis & therapy (2021)
The OncoBEAMTM EGFR V2 is a sensitive, robust, and accurate assay that delivers reproducible results. Next-generation sequencing and BEAMing technologies act complementarily in the routine molecular screening. We show that using a next-generation sequencing assay, despite its lower sensitivity, enables the identification of rare EGFR alterations or resistance mechanisms (mutation, deletion, insertion, and copy number variation) to orient first- and second-line treatments.
Keyphrases
  • copy number
  • small cell lung cancer
  • mitochondrial dna
  • epidermal growth factor receptor
  • tyrosine kinase
  • genome wide
  • high throughput
  • clinical practice
  • dna methylation
  • single molecule
  • bioinformatics analysis