<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Balbach ML</submitter><funding>NCI NIH HHS</funding><funding>National Comprehensive Cancer Network</funding><pagination>100306</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9010630</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(5)</volume><pubmed_abstract>The application of KRAS G12C inhibitors in the setting of NSCLC represents a major milestone for a previously "undruggable" target. Here, we present the second reported case of de novo &lt;i>KRAS&lt;/i> G12C-mutant primary SCLC. Would our patient benefit from a KRAS G12C inhibitor?</pubmed_abstract><journal>JTO clinical and research reports</journal><pubmed_title>De Novo &lt;i>KRAS&lt;/i> G12C-Mutant SCLC: A Case Report.</pubmed_title><pmcid>PMC9010630</pmcid><funding_grant_id>K12 CA090625</funding_grant_id><funding_grant_id>030763</funding_grant_id><pubmed_authors>Eisenberg R</pubmed_authors><pubmed_authors>Balbach ML</pubmed_authors><pubmed_authors>Iams WT</pubmed_authors></additional><is_claimable>false</is_claimable><name>De Novo &lt;i>KRAS&lt;/i> G12C-Mutant SCLC: A Case Report.</name><description>The application of KRAS G12C inhibitors in the setting of NSCLC represents a major milestone for a previously "undruggable" target. Here, we present the second reported case of de novo &lt;i>KRAS&lt;/i> G12C-mutant primary SCLC. Would our patient benefit from a KRAS G12C inhibitor?</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-04T19:31:56.906Z</modification><creation>2025-02-19T02:58:41.347Z</creation></dates><accession>S-EPMC9010630</accession><cross_references><pubmed>35434667</pubmed><doi>10.1016/j.jtocrr.2022.100306</doi></cross_references></HashMap>