<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li N</submitter><funding>NCATS NIH HHS</funding><funding>NIH Clinical Center</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>1240</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7393232</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10</volume><pubmed_abstract>&lt;b>Background:&lt;/b> The longitudinal monitoring of actionable oncogenes in circulating tumor DNA (ctDNA) of non-small cell lung cancer (NSCLC) is crucial for clinicians to evaluate current therapeutic response and adjust therapeutic strategies. Saliva-based electric field-induced release and measurement (EFIRM) is liquid biopsy platform to that can directly detect mutation genes with a small volume of samples. Herein, we compared the effectiveness of longitudinal monitoring for the combination of epidermal growth factor receptor (&lt;i>EGFR)&lt;/i> and phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha (&lt;i>PIK3CA)&lt;/i> mutations between saliva-based EFIRM and plasma-based platforms (ddPCR and NGS) in two advanced NSCLC patients undergoing the treatment with osimertinib before </pubmed_abstract><journal>Frontiers in oncology</journal><pubmed_title>Longitudinal Monitoring of &lt;i>EGFR&lt;/i> and &lt;i>PIK3CA&lt;/i> Mutations by Saliva-Based EFIRM in Advanced NSCLC Patients With Local Ablative Therapy and Osimertinib Treatment: Two Case Reports.</pubmed_title><pmcid>PMC7393232</pmcid><funding_grant_id>U01 CA233370</funding_grant_id><funding_grant_id>UH3 CA206126</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>Kim C</pubmed_authors><pubmed_authors>Ye L</pubmed_authors><pubmed_authors>Wong DTW</pubmed_authors><pubmed_authors>Guha U</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Wei F</pubmed_authors><pubmed_authors>Chia D</pubmed_authors><pubmed_authors>Li N</pubmed_authors><pubmed_authors>Cheng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Longitudinal Monitoring of &lt;i>EGFR&lt;/i> and &lt;i>PIK3CA&lt;/i> Mutations by Saliva-Based EFIRM in Advanced NSCLC Patients With Local Ablative Therapy and Osimertinib Treatment: Two Case Reports.</name><description>&lt;b>Background:&lt;/b> The longitudinal monitoring of actionable oncogenes in circulating tumor DNA (ctDNA) of non-small cell lung cancer (NSCLC) is crucial for clinicians to evaluate current therapeutic response and adjust therapeutic strategies. Saliva-based electric field-induced release and measurement (EFIRM) is liquid biopsy platform to that can directly detect mutation genes with a small volume of samples. Herein, we compared the effectiveness of longitudinal monitoring for the combination of epidermal growth factor receptor (&lt;i>EGFR)&lt;/i> and phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha (&lt;i>PIK3CA)&lt;/i> mutations between saliva-based EFIRM and plasma-based platforms (ddPCR and NGS) in two advanced NSCLC patients undergoing the treatment with osimertinib before </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-05-02T15:31:13.69Z</modification><creation>2020-08-20T07:18:33Z</creation></dates><accession>S-EPMC7393232</accession><cross_references><pubmed>32793495</pubmed><doi>10.3389/fonc.2020.01240</doi></cross_references></HashMap>