<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ruppert AM</submitter><funding>Roche</funding><funding>Novartis, France</funding><funding>Institut National Du Cancer, France</funding><funding>AstraZeneca</funding><pagination>100052</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8474404</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>1(3)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>&lt;i>KRAS&lt;/i> mutations are detected in 20% to 30% of NSCLC. However, &lt;i>KRAS&lt;/i> mutation subtypes may differently influence the outcome of patients with advanced NSCLC.&lt;h4>Methods&lt;/h4>In the Biomarkers France study, 4894 &lt;i>KRAS&lt;/i> mutations (26.2%) were detected in 4634 patients from the 17,664 enrolled patients with NSCLC. Survival and treatment data on noncurative stage III to IV NSCLC were available for 901 patients. First- and second-line treatment effects on progression-free survival and overall survival were analyzed according to the &lt;i>KRAS&lt;/i> mutations subtype.&lt;h4>Results&lt;/h4>Over 95% of patients with &lt;i>KRAS&lt;/i> mutation were smokers or former smokers who were white (99.5%), presenting with adenocarcinoma (82.5%). The most common &lt;i>KRAS&lt;/i> mutation subtyp</pubmed_abstract><journal>JTO clinical and research reports</journal><pubmed_title>Outcomes of Patients With Advanced NSCLC From the Intergroupe Francophone de Cancerologie Thoracique Biomarkers France Study by &lt;i>KRAS&lt;/i> Mutation Subtypes.</pubmed_title><pmcid>PMC8474404</pmcid><funding_grant_id>2011-038</funding_grant_id><pubmed_authors>Bringuier PP</pubmed_authors><pubmed_authors>Debieuvre D</pubmed_authors><pubmed_authors>Foucher P</pubmed_authors><pubmed_authors>Janicot H</pubmed_authors><pubmed_authors>Barlesi F</pubmed_authors><pubmed_authors>Westeel V</pubmed_authors><pubmed_authors>Ricordel C</pubmed_authors><pubmed_authors>Poudenx M</pubmed_authors><pubmed_authors>Escande F</pubmed_authors><pubmed_authors>Beau-Faller M</pubmed_authors><pubmed_authors>Ouafik L</pubmed_authors><pubmed_authors>Rouquette I</pubmed_authors><pubmed_authors>Lemoine A</pubmed_authors><pubmed_authors>Merlio JP</pubmed_authors><pubmed_authors>Ruppert AM</pubmed_authors><pubmed_authors>Mazieres J</pubmed_authors><pubmed_authors>Monnet I</pubmed_authors><pubmed_authors>Morin F</pubmed_authors><pubmed_authors>Langlais A</pubmed_authors><pubmed_authors>Souquet PJ</pubmed_authors><pubmed_authors>Wislez M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outcomes of Patients With Advanced NSCLC From the Intergroupe Francophone de Cancerologie Thoracique Biomarkers France Study by &lt;i>KRAS&lt;/i> Mutation Subtypes.</name><description>&lt;h4>Introduction&lt;/h4>&lt;i>KRAS&lt;/i> mutations are detected in 20% to 30% of NSCLC. However, &lt;i>KRAS&lt;/i> mutation subtypes may differently influence the outcome of patients with advanced NSCLC.&lt;h4>Methods&lt;/h4>In the Biomarkers France study, 4894 &lt;i>KRAS&lt;/i> mutations (26.2%) were detected in 4634 patients from the 17,664 enrolled patients with NSCLC. Survival and treatment data on noncurative stage III to IV NSCLC were available for 901 patients. First- and second-line treatment effects on progression-free survival and overall survival were analyzed according to the &lt;i>KRAS&lt;/i> mutations subtype.&lt;h4>Results&lt;/h4>Over 95% of patients with &lt;i>KRAS&lt;/i> mutation were smokers or former smokers who were white (99.5%), presenting with adenocarcinoma (82.5%). The most common &lt;i>KRAS&lt;/i> mutation subtyp</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2025-06-01T00:32:05.837Z</modification><creation>2025-06-01T00:32:05.837Z</creation></dates><accession>S-EPMC8474404</accession><cross_references><pubmed>34589947</pubmed><doi>10.1016/j.jtocrr.2020.100052</doi></cross_references></HashMap>