<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(3)</volume><submitter>Di Federico A</submitter><pubmed_abstract>Epidermal growth factor receptor (&lt;i>EGFR&lt;/i>) gene fusions represent an extremely rare aberration, occurring in approximately 0.05-0.13% non-small cell lung cancer (NSCLC) patients. &lt;i>RAD51&lt;/i> is the most frequently involved partner gene in &lt;i>EGFR&lt;/i> fusions, but other fusion partner genes have been described. To date, a considerable number of next-generation sequencing (NGS) panels still cannot detect these alterations due to the position of the breakpoint site, mainly involving intron 24 of &lt;i>EGFR&lt;/i>. Current evidences show that such gene alteration is more likely to occur in lung adenocarcinomas of young, female, non-smoker patients. Also, brain metastases are frequently reported in these patients. Only very few cases in literature described clinical characteristics and outcomes </pubmed_abstract><journal>Translational lung cancer research</journal><pagination>497-503</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8988076</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>EGFR&lt;/i>-&lt;i>RAD51&lt;/i> gene fusion NSCLC responsiveness to different generation EGFR-TKIs: two cases and review of the literature.</pubmed_title><pmcid>PMC8988076</pmcid><pubmed_authors>Di Federico A</pubmed_authors><pubmed_authors>Gelsomino F</pubmed_authors><pubmed_authors>De Giglio A</pubmed_authors><pubmed_authors>Palladini A</pubmed_authors><pubmed_authors>Giusti R</pubmed_authors><pubmed_authors>Ardizzoni A</pubmed_authors><pubmed_authors>Piras M</pubmed_authors><pubmed_authors>Filetti M</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>EGFR&lt;/i>-&lt;i>RAD51&lt;/i> gene fusion NSCLC responsiveness to different generation EGFR-TKIs: two cases and review of the literature.</name><description>Epidermal growth factor receptor (&lt;i>EGFR&lt;/i>) gene fusions represent an extremely rare aberration, occurring in approximately 0.05-0.13% non-small cell lung cancer (NSCLC) patients. &lt;i>RAD51&lt;/i> is the most frequently involved partner gene in &lt;i>EGFR&lt;/i> fusions, but other fusion partner genes have been described. To date, a considerable number of next-generation sequencing (NGS) panels still cannot detect these alterations due to the position of the breakpoint site, mainly involving intron 24 of &lt;i>EGFR&lt;/i>. Current evidences show that such gene alteration is more likely to occur in lung adenocarcinomas of young, female, non-smoker patients. Also, brain metastases are frequently reported in these patients. Only very few cases in literature described clinical characteristics and outcomes </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T10:45:19.906Z</modification><creation>2025-04-04T10:45:19.906Z</creation></dates><accession>S-EPMC8988076</accession><cross_references><pubmed>35399574</pubmed><doi>10.21037/tlcr-21-888</doi></cross_references></HashMap>