<HashMap><database>biostudies-literature</database><scores/><additional><submitter>McCoach CE</submitter><funding>University of Colorado Lung Cancer SPORE</funding><funding>NCI NIH HHS</funding><pagination>2758-2770</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6157019</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(12)</volume><pubmed_abstract>&lt;b>Purpose:&lt;/b> Patients with advanced non-small cell lung cancer (NSCLC) whose tumors harbor anaplastic lymphoma kinase (&lt;i>ALK)&lt;/i> gene fusions benefit from treatment with ALK inhibitors (ALKi). Analysis of cell-free circulating tumor DNA (cfDNA) may provide a noninvasive way to identify &lt;i>ALK&lt;/i> fusions and actionable resistance mechanisms without an invasive biopsy.&lt;b>Patients and Methods:&lt;/b> The Guardant360 (G360; Guardant Health) deidentified database of NSCLC cases was queried to identify 88 consecutive patients with 96 plasma-detected &lt;i>ALK&lt;/i> fusions. G360 is a clinical cfDNA next-generation sequencing (NGS) test that detects point mutations, select copy number gains, fusions, insertions, and deletions in plasma.&lt;b>Results:&lt;/b> Identified fusion partners included &lt;i>EML4&lt;/i></pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Clinical Utility of Cell-Free DNA for the Detection of &lt;i>ALK&lt;/i> Fusions and Genomic Mechanisms of ALK Inhibitor Resistance in Non-Small Cell Lung Cancer.</pubmed_title><pmcid>PMC6157019</pmcid><funding_grant_id>P50 CA058187</funding_grant_id><funding_grant_id>P30 CA046934</funding_grant_id><funding_grant_id>P50CA058187</funding_grant_id><funding_grant_id>R01 CA193935</funding_grant_id><pubmed_authors>Waqar SN</pubmed_authors><pubmed_authors>Shaw AT</pubmed_authors><pubmed_authors>McCoach CE</pubmed_authors><pubmed_authors>Le AT</pubmed_authors><pubmed_authors>Levy B</pubmed_authors><pubmed_authors>Purcell WT</pubmed_authors><pubmed_authors>Chue BM</pubmed_authors><pubmed_authors>Blakely CM</pubmed_authors><pubmed_authors>Davies KD</pubmed_authors><pubmed_authors>Lanman RB</pubmed_authors><pubmed_authors>Banks KC</pubmed_authors><pubmed_authors>Diaz J</pubmed_authors><pubmed_authors>Aisner DL</pubmed_authors><pubmed_authors>Raymond VM</pubmed_authors><pubmed_authors>Doebele RC</pubmed_authors><pubmed_authors>Lee CE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical Utility of Cell-Free DNA for the Detection of &lt;i>ALK&lt;/i> Fusions and Genomic Mechanisms of ALK Inhibitor Resistance in Non-Small Cell Lung Cancer.</name><description>&lt;b>Purpose:&lt;/b> Patients with advanced non-small cell lung cancer (NSCLC) whose tumors harbor anaplastic lymphoma kinase (&lt;i>ALK)&lt;/i> gene fusions benefit from treatment with ALK inhibitors (ALKi). Analysis of cell-free circulating tumor DNA (cfDNA) may provide a noninvasive way to identify &lt;i>ALK&lt;/i> fusions and actionable resistance mechanisms without an invasive biopsy.&lt;b>Patients and Methods:&lt;/b> The Guardant360 (G360; Guardant Health) deidentified database of NSCLC cases was queried to identify 88 consecutive patients with 96 plasma-detected &lt;i>ALK&lt;/i> fusions. G360 is a clinical cfDNA next-generation sequencing (NGS) test that detects point mutations, select copy number gains, fusions, insertions, and deletions in plasma.&lt;b>Results:&lt;/b> Identified fusion partners included &lt;i>EML4&lt;/i></description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2025-04-04T11:20:49.222Z</modification><creation>2019-03-27T00:11:25Z</creation></dates><accession>S-EPMC6157019</accession><cross_references><pubmed>29599410</pubmed><doi>10.1158/1078-0432.CCR-17-2588</doi><doi>10.1158/1078-0432.ccr-17-2588</doi></cross_references></HashMap>