<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(7)</volume><submitter>Zhang Z</submitter><pubmed_abstract>Objective: To detect the serum epithelial growth factor receptor (EGFR) gene mutation status in patients with lung cancer via second-generation sequencing and to analyze its correlations with the clinical features of patients and its therapeutic effects. Methods: A total of 110 patients with non-small cell lung cancer (NSCLC) treated in our hospital were recruited as subjects of our study. The distribution of the EGFR gene mutation in patients was detected via second-generation sequencing and then patients were divided into mutant-type EGFR group (n=37) and wild-type EGFR group (n=73). The clinical features and therapeutic effects were compared between the two groups of patients. Results: A total of 5 kinds of EGFR gene mutation [19del (45.95%), L858R (43.24%), L861Q (5.41%), S768I (2.70%)</pubmed_abstract><journal>International journal of clinical and experimental pathology</journal><pagination>3551-3558</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6962891</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Serum EGFR gene mutation status via second-generation sequencing and clinical features of patients with advanced lung cancer.</pubmed_title><pmcid>PMC6962891</pmcid><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Zhou S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Serum EGFR gene mutation status via second-generation sequencing and clinical features of patients with advanced lung cancer.</name><description>Objective: To detect the serum epithelial growth factor receptor (EGFR) gene mutation status in patients with lung cancer via second-generation sequencing and to analyze its correlations with the clinical features of patients and its therapeutic effects. Methods: A total of 110 patients with non-small cell lung cancer (NSCLC) treated in our hospital were recruited as subjects of our study. The distribution of the EGFR gene mutation in patients was detected via second-generation sequencing and then patients were divided into mutant-type EGFR group (n=37) and wild-type EGFR group (n=73). The clinical features and therapeutic effects were compared between the two groups of patients. Results: A total of 5 kinds of EGFR gene mutation [19del (45.95%), L858R (43.24%), L861Q (5.41%), S768I (2.70%)</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-26T16:47:12.233Z</modification><creation>2020-05-22T08:27:45Z</creation></dates><accession>S-EPMC6962891</accession><cross_references><pubmed>31949733</pubmed></cross_references></HashMap>