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ABSTRACT: Background
The tumor mutational burden (TMB) is a promising biomarker for immune checkpoint inhibitor (ICI). However, its relationships with clinical parameters have not been fully explored. We aimed to assess potential factors including age, microsatellite instability (MSI) state, tumor types, and gene mutations that might influence TMB value through analyzing 1,504 tissue samples and 496 blood samples from cancer patients.Methods
The TMB value of individual samples was calculated by whole-exome sequencing (WES) analysis and major cancer-related gene mutations were evaluated using panel sequencing. MSI was detected with MSI analysis system.Results
The results showed that for blood samples, compared to age 1 (age ≤56 years old) or age 2 (56< age <68 years old) group
SUBMITTER: Li L
PROVIDER: S-EPMC8908122 | biostudies-literature | 2022 Feb
REPOSITORIES: biostudies-literature