<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang X</submitter><funding>Beijing Youth Program for Outstanding Talents</funding><funding>Beijing Medical Award Foundation Youth Committee of Lung Cancer Crowd-funding Project</funding><funding>Beijing Hospitals Authority Youth Programme</funding><funding>Beijing Municipal Administration of Hospitals Incubating Program</funding><pagination>1107</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8520304</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>EGFR and ALK alternations often contribute to human malignancies, including lung cancer. EGFR and ALK mutations are usually sensitive to EGFR-tyrosine kinase inhibitors (TKIs) and ALK-TKIs. Although generally mutually exclusive, these mutations do co-exist in rare cases. This study investigated the frequencies, clinical characteristics, therapeutic efficacies, and genetic profiles of lung cancer patients with EGFR and ALK co-mutations.&lt;h4>Methods&lt;/h4>Patients with concurrent EGFR and ALK mutations were included in this study, which analyzed mutation profiles and treatment histories. SPSS20.0 were used for survival analysis.&lt;h4>Results&lt;/h4>Among 271 ALK-positive (ALK-pos) and 2975 EGFR-positive (EGFR-pos) patients in our database, nine (2.6% of ALK-pos and 0.2% of EGFR-po</pubmed_abstract><journal>BMC cancer</journal><pubmed_title>Genetic and treatment profiles of patients with concurrent Epidermal Growth Factor Receptor (EGFR) and Anaplastic Lymphoma Kinase (ALK) mutations.</pubmed_title><pmcid>PMC8520304</pmcid><funding_grant_id>PX2019038</funding_grant_id><funding_grant_id>202001001</funding_grant_id><funding_grant_id>QML20191112</funding_grant_id><funding_grant_id>2018000021469G262</funding_grant_id><funding_grant_id>PX2020044</funding_grant_id><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Zhuo M</pubmed_authors><pubmed_authors>Xia X</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Zhong J</pubmed_authors><pubmed_authors>Yu Z</pubmed_authors><pubmed_authors>Chen R</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic and treatment profiles of patients with concurrent Epidermal Growth Factor Receptor (EGFR) and Anaplastic Lymphoma Kinase (ALK) mutations.</name><description>&lt;h4>Background&lt;/h4>EGFR and ALK alternations often contribute to human malignancies, including lung cancer. EGFR and ALK mutations are usually sensitive to EGFR-tyrosine kinase inhibitors (TKIs) and ALK-TKIs. Although generally mutually exclusive, these mutations do co-exist in rare cases. This study investigated the frequencies, clinical characteristics, therapeutic efficacies, and genetic profiles of lung cancer patients with EGFR and ALK co-mutations.&lt;h4>Methods&lt;/h4>Patients with concurrent EGFR and ALK mutations were included in this study, which analyzed mutation profiles and treatment histories. SPSS20.0 were used for survival analysis.&lt;h4>Results&lt;/h4>Among 271 ALK-positive (ALK-pos) and 2975 EGFR-positive (EGFR-pos) patients in our database, nine (2.6% of ALK-pos and 0.2% of EGFR-po</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-22T11:27:11.662Z</modification><creation>2025-04-05T23:58:42.005Z</creation></dates><accession>S-EPMC8520304</accession><cross_references><pubmed>34654390</pubmed><doi>10.1186/s12885-021-08824-2</doi></cross_references></HashMap>