<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li F</submitter><funding>National Institutes of Health</funding><pagination>E2041</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7464208</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(8)</volume><pubmed_abstract>Mutations identified in the epidermal growth factor receptor (EGFR) predict sensitivity to EGFR-targeted therapy for non-small cell lung carcinoma (NSCLC). We previously reported that Electric Field-Induced Release and Measurement (EFIRM)-based liquid biopsy could detect EGFR ctDNA with >94% concordance with tissue-based genotyping. A side-by-side comparison of concordance of EFIRM and droplet digital PCR (ddPCR) for the detection of the two front-line actionable EFGR mutations was performed with paired plasma and saliva samples from 13 NSCLC patients. Deep sequencing analysis based on single-strand DNA library preparation was employed to determine the size distributions of EGFR L858R ctDNA in plasma and saliva samples. EFIRM detected both EGFR mutations with 100% sensitivity in both plasm</pubmed_abstract><journal>Cancers</journal><pubmed_title>Ultra-Short Circulating Tumor DNA (usctDNA) in Plasma and Saliva of Non-Small Cell Lung Cancer (NSCLC) Patients.</pubmed_title><pmcid>PMC7464208</pmcid><funding_grant_id>U01 CA233370</funding_grant_id><funding_grant_id>UH2 CA206126</funding_grant_id><funding_grant_id>UH3 TR000923</funding_grant_id><funding_grant_id>R21 CA239052</funding_grant_id><pubmed_authors>Yan Q</pubmed_authors><pubmed_authors>Feng Z</pubmed_authors><pubmed_authors>Lin CC</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Liao W</pubmed_authors><pubmed_authors>Tu M</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Su WC</pubmed_authors><pubmed_authors>Wong DTW</pubmed_authors><pubmed_authors>Tang JH</pubmed_authors><pubmed_authors>Wei F</pubmed_authors><pubmed_authors>Huang WL</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Shen MM</pubmed_authors><pubmed_authors>Chia D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultra-Short Circulating Tumor DNA (usctDNA) in Plasma and Saliva of Non-Small Cell Lung Cancer (NSCLC) Patients.</name><description>Mutations identified in the epidermal growth factor receptor (EGFR) predict sensitivity to EGFR-targeted therapy for non-small cell lung carcinoma (NSCLC). We previously reported that Electric Field-Induced Release and Measurement (EFIRM)-based liquid biopsy could detect EGFR ctDNA with >94% concordance with tissue-based genotyping. A side-by-side comparison of concordance of EFIRM and droplet digital PCR (ddPCR) for the detection of the two front-line actionable EFGR mutations was performed with paired plasma and saliva samples from 13 NSCLC patients. Deep sequencing analysis based on single-strand DNA library preparation was employed to determine the size distributions of EGFR L858R ctDNA in plasma and saliva samples. EFIRM detected both EGFR mutations with 100% sensitivity in both plasm</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-22T15:01:39.777Z</modification><creation>2020-09-09T07:09:16Z</creation></dates><accession>S-EPMC7464208</accession><cross_references><pubmed>32722209</pubmed><doi>10.3390/cancers12082041</doi></cross_references></HashMap>