<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Peng TR</submitter><funding>Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation</funding><pagination>3676</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11545475</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(21)</volume><pubmed_abstract>&lt;b>Background&lt;/b>: The KRAS G12C mutation, prevalent in various malignancies, including non-small cell lung cancer (NSCLC), represents a unique therapeutic target. Adagrasib and sotorasib, two FDA-approved agents specifically targeting this mutation, have shown promise in clinical trials. This study aims to compare their efficacy in treating KRAS G12C-mutated NSCLC, drawing insights from pivotal clinical trials. &lt;b>Methods&lt;/b>: We analyzed data from three key clinical trials: KRYSTAL-1, CodeBreak100, and CodeBreak200. Our methodology involved reconstructing individual patient data from published Kaplan-Meier curves using the IPDfromKM tool (Version 0.1.10). The primary endpoints were progression-free survival (PFS) and overall survival (OS), evaluated through hazard ratios (HRs) and the re</pubmed_abstract><journal>Cancers</journal><pubmed_title>Comparative Efficacy of Adagrasib and Sotorasib in KRAS G12C-Mutant NSCLC: Insights from Pivotal Trials.</pubmed_title><pmcid>PMC11545475</pmcid><funding_grant_id>TCRD-TPE-113-50</funding_grant_id><funding_grant_id>TCRD-TPE-113-54</funding_grant_id><pubmed_authors>Yi TY</pubmed_authors><pubmed_authors>Wu AJ</pubmed_authors><pubmed_authors>Peng TR</pubmed_authors><pubmed_authors>Wu TW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative Efficacy of Adagrasib and Sotorasib in KRAS G12C-Mutant NSCLC: Insights from Pivotal Trials.</name><description>&lt;b>Background&lt;/b>: The KRAS G12C mutation, prevalent in various malignancies, including non-small cell lung cancer (NSCLC), represents a unique therapeutic target. Adagrasib and sotorasib, two FDA-approved agents specifically targeting this mutation, have shown promise in clinical trials. This study aims to compare their efficacy in treating KRAS G12C-mutated NSCLC, drawing insights from pivotal clinical trials. &lt;b>Methods&lt;/b>: We analyzed data from three key clinical trials: KRYSTAL-1, CodeBreak100, and CodeBreak200. Our methodology involved reconstructing individual patient data from published Kaplan-Meier curves using the IPDfromKM tool (Version 0.1.10). The primary endpoints were progression-free survival (PFS) and overall survival (OS), evaluated through hazard ratios (HRs) and the re</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-04-08T19:44:59.602Z</modification><creation>2025-04-19T17:29:05.305Z</creation></dates><accession>S-EPMC11545475</accession><cross_references><pubmed>39518114</pubmed><doi>10.3390/cancers16213676</doi></cross_references></HashMap>