<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(32)</volume><submitter>Hsiao SH</submitter><pubmed_abstract>Non-small cell lung cancer (NSCLC) patients tend to develop brain metastases (BM), but the link between BM occurrence and driver mutations in NSCLC is not very clear. We explored whether activating mutations of epidermal growth factor receptors (&lt;i>EGFRs&lt;/i>) in exon 19 deletion or L858R predict BM in NSCLC. A retrospective multivariable logistic regression analysis of 384 patients demonstrated that the presence of mutated-&lt;i>EGFRs&lt;/i> was associated with overall BM (OR=2.24, P=0.001) compared to that of wild-type &lt;i>EGFR&lt;/i> (WT-&lt;i>EGFR&lt;/i>). Moreover, the time-to-event analysis model considering death as a competing risk revealed that, irrespective of survival, mutated-&lt;i>EGFR&lt;/i>s predicted subsequent BM (SBM) in stage IIIB-IV patients (37.1% &lt;i>vs&lt;/i>. 10.6%, HR=2.98, P=0.002) after ad</pubmed_abstract><journal>Oncotarget</journal><pagination>53405-53418</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5581119</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Brain metastases in patients with non-small cell lung cancer: the role of mutated-&lt;i>EGFRs&lt;/i> with an exon 19 deletion or L858R point mutation in cancer cell dissemination.</pubmed_title><pmcid>PMC5581119</pmcid><pubmed_authors>Hsu RC</pubmed_authors><pubmed_authors>Kao YR</pubmed_authors><pubmed_authors>Liu HE</pubmed_authors><pubmed_authors>Wu CW</pubmed_authors><pubmed_authors>Chou YT</pubmed_authors><pubmed_authors>Lin SE</pubmed_authors><pubmed_authors>Chung CL</pubmed_authors><pubmed_authors>Hsiao SH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Brain metastases in patients with non-small cell lung cancer: the role of mutated-&lt;i>EGFRs&lt;/i> with an exon 19 deletion or L858R point mutation in cancer cell dissemination.</name><description>Non-small cell lung cancer (NSCLC) patients tend to develop brain metastases (BM), but the link between BM occurrence and driver mutations in NSCLC is not very clear. We explored whether activating mutations of epidermal growth factor receptors (&lt;i>EGFRs&lt;/i>) in exon 19 deletion or L858R predict BM in NSCLC. A retrospective multivariable logistic regression analysis of 384 patients demonstrated that the presence of mutated-&lt;i>EGFRs&lt;/i> was associated with overall BM (OR=2.24, P=0.001) compared to that of wild-type &lt;i>EGFR&lt;/i> (WT-&lt;i>EGFR&lt;/i>). Moreover, the time-to-event analysis model considering death as a competing risk revealed that, irrespective of survival, mutated-&lt;i>EGFR&lt;/i>s predicted subsequent BM (SBM) in stage IIIB-IV patients (37.1% &lt;i>vs&lt;/i>. 10.6%, HR=2.98, P=0.002) after ad</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2025-04-19T22:18:54.701Z</modification><creation>2019-03-27T02:55:14Z</creation></dates><accession>S-EPMC5581119</accession><cross_references><pubmed>28881820</pubmed><doi>10.18632/oncotarget.18509</doi></cross_references></HashMap>