<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(10)</volume><submitter>Wang MM</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Kirsten rat sarcoma viral oncogene homolog (&lt;i>KRAS&lt;/i>) mutation seemingly suffered less effective therapeutic regimens in the absence of widely-accepted targeted drugs compared with other mutation types in non-small cell lung cancer (NSCLC). However, whether these non-selective therapy schedules for &lt;i>KRAS&lt;/i> mutation matters is still under debate. Correspondingly, we aimed to compare the long term expectancy of indicated therapeutic regimes and further explore the optimal schemes of &lt;i>KRAS&lt;/i> mutated NSCLC in the absence of targeted drugs in this retrospective study cohort.&lt;h4>Methods&lt;/h4>We conducted a single-center retrospective analysis among 66 patients diagnosed with &lt;i>KRAS&lt;/i>-mutant advanced NSCLC from November 2018 to December 2020. These enrolled cases w</pubmed_abstract><journal>Translational lung cancer research</journal><pagination>2030-2039</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10654440</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical outcomes of &lt;i>KRAS&lt;/i>-mutant non-small cell lung cancer under untargeted therapeutic regimes in the real world: a retrospective observational study.</pubmed_title><pmcid>PMC10654440</pmcid><pubmed_authors>Shan HL</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Wu S</pubmed_authors><pubmed_authors>Qu SY</pubmed_authors><pubmed_authors>Yang XM</pubmed_authors><pubmed_authors>Wang MM</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Song LQ</pubmed_authors><pubmed_authors>Zhang SY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical outcomes of &lt;i>KRAS&lt;/i>-mutant non-small cell lung cancer under untargeted therapeutic regimes in the real world: a retrospective observational study.</name><description>&lt;h4>Background&lt;/h4>Kirsten rat sarcoma viral oncogene homolog (&lt;i>KRAS&lt;/i>) mutation seemingly suffered less effective therapeutic regimens in the absence of widely-accepted targeted drugs compared with other mutation types in non-small cell lung cancer (NSCLC). However, whether these non-selective therapy schedules for &lt;i>KRAS&lt;/i> mutation matters is still under debate. Correspondingly, we aimed to compare the long term expectancy of indicated therapeutic regimes and further explore the optimal schemes of &lt;i>KRAS&lt;/i> mutated NSCLC in the absence of targeted drugs in this retrospective study cohort.&lt;h4>Methods&lt;/h4>We conducted a single-center retrospective analysis among 66 patients diagnosed with &lt;i>KRAS&lt;/i>-mutant advanced NSCLC from November 2018 to December 2020. These enrolled cases w</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2026-06-03T09:46:25.308Z</modification><creation>2025-04-05T10:23:25.872Z</creation></dates><accession>S-EPMC10654440</accession><cross_references><pubmed>38025817</pubmed><doi>10.21037/tlcr-23-449</doi></cross_references></HashMap>