Ontology highlight
ABSTRACT: Background
Esophageal cancer (EC) is an aggressive malignant tumor with poor prognosis and high incidence. It is the sixth leading cause of cancer-related death in the world, and the 5-year overall survival (OS) rate is only 12-20%. The rapid development of next-generation sequencing (NGS) has provided powerful help for the treatment and management of EC patients.Methods
Tumor tissue and blood samples of 43 Chinese patients with nonsurgical esophageal squamous cell carcinoma (ESCC) were sequenced using a 425 gene-panel. Genomic profiling was explored and and the Cox proportional hazards model was used to analyze the correlations between gene or signaling pathway alterations and prognosis.Results
In this study, the most common mutated genes were TP53 (90.5%),
SUBMITTER: Zhou X
PROVIDER: S-EPMC11009591 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature