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ABSTRACT: Background
The clinical impact of SMARCA4 mutations (SMARCA4ms) in gastroesophageal adenocarcinoma (GEA) remains underexplored. This study aimed to examine the association of SMARCA4ms with clinical outcomes and co-occurrence with other gene mutations identified through a next-generation sequencing (NGS) panel in GEA patients.Methods
A total of 256 patients with metastatic or recurrent GEA who underwent NGS panel profiling at the MD Anderson Cancer Center between 2016 and 2022 were included. Comparative analyses were performed to assess clinical outcomes related to SMARCA4ms. The frequency and types of SMARCA4ms and their co-occurrence with other gene mutations were also examined.Results
SMARCA4ms were identified in 19 patients (7.4%). These SMARCA4ms were significa
SUBMITTER: Yamashita K
PROVIDER: S-EPMC11010836 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature