<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25(2)</volume><submitter>Garcia J</submitter><pubmed_abstract>&lt;h4>Background and objectives&lt;/h4>The use of ultra-sensitive diagnostic tests to detect clinically actionable somatic alterations within the gene encoding the epidermal growth factor receptor (EGFR) within circulating cell-free DNA is an important first step in determining the eligibility of patients with non-small cell lung cancer to receive tyrosine kinase inhibitors.&lt;h4>Methods&lt;/h4>We present the clinical validation (accuracy, sensitivity, and specificity) of a highly sensitive OncoBEAM&lt;sup>TM&lt;/sup> EGFR V2 test, which we compare to a custom next-generation sequencing assay, for the treatment of patients with non-small cell lung cancer with EGFR tyrosine kinase inhibitor therapies. The OncoBEAM&lt;sup>TM&lt;/sup> digital-polymerase chain reaction method detects 36 different EGFR alterations i</pubmed_abstract><journal>Molecular diagnosis &amp; therapy</journal><pagination>239-250</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7956937</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Routine Molecular Screening of Patients with Advanced Non-SmallCell Lung Cancer in Circulating Cell-Free DNA at Diagnosis and During Progression Using OncoBEAM&lt;sup>TM&lt;/sup> EGFR V2 and NGS Technologies.</pubmed_title><pmcid>PMC7956937</pmcid><pubmed_authors>Couraud S</pubmed_authors><pubmed_authors>Duruisseau M</pubmed_authors><pubmed_authors>Payen L</pubmed_authors><pubmed_authors>Barthelemy D</pubmed_authors><pubmed_authors>Geiguer F</pubmed_authors><pubmed_authors>Gauthier A</pubmed_authors><pubmed_authors>Garcia J</pubmed_authors><pubmed_authors>Merle P</pubmed_authors><pubmed_authors>Balandier J</pubmed_authors><pubmed_authors>Jones FS</pubmed_authors><pubmed_authors>Holtrup F</pubmed_authors><pubmed_authors>Edelstein DL</pubmed_authors><pubmed_authors>Grolleau E</pubmed_authors><pubmed_authors>Lescuyer G</pubmed_authors><pubmed_authors>Rodriguez-Lafrasse C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Routine Molecular Screening of Patients with Advanced Non-SmallCell Lung Cancer in Circulating Cell-Free DNA at Diagnosis and During Progression Using OncoBEAM&lt;sup>TM&lt;/sup> EGFR V2 and NGS Technologies.</name><description>&lt;h4>Background and objectives&lt;/h4>The use of ultra-sensitive diagnostic tests to detect clinically actionable somatic alterations within the gene encoding the epidermal growth factor receptor (EGFR) within circulating cell-free DNA is an important first step in determining the eligibility of patients with non-small cell lung cancer to receive tyrosine kinase inhibitors.&lt;h4>Methods&lt;/h4>We present the clinical validation (accuracy, sensitivity, and specificity) of a highly sensitive OncoBEAM&lt;sup>TM&lt;/sup> EGFR V2 test, which we compare to a custom next-generation sequencing assay, for the treatment of patients with non-small cell lung cancer with EGFR tyrosine kinase inhibitor therapies. The OncoBEAM&lt;sup>TM&lt;/sup> digital-polymerase chain reaction method detects 36 different EGFR alterations i</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2026-05-07T12:02:03.435Z</modification><creation>2022-02-09T08:14:40.384Z</creation></dates><accession>S-EPMC7956937</accession><cross_references><pubmed>33660188</pubmed><doi>10.1007/s40291-021-00515-9</doi></cross_references></HashMap>