| Literature DB >> 28197377 |
Diane Goltz1, Heidrun Gevensleben1, Jörn Dietrich2, Dimo Dietrich3.
Abstract
This study evaluates promoter methylation of the programmed cell death ligand 1 (PD-L1) as a biomarker in a cohort of 383 colorectal cancer patients. PD-L1 methylation (mPD-L1) was inversely correlated with PD-L1 mRNA expression (p = 0.001) and was associated with significantly shorter overall survival (OS, p = 0.003) and recurrence-free survival (RFS, p < 0.001). In age-stratified multivariate Cox proportional hazards analyses including sex, tumor, nodal, distant metastasis categories, microsatellite instability (MSI)-status, and PD-L1 mRNA, mPD-L1 is classified as an independent prognostic factor (OS: p = 0.030; RFS: p < 0.001). Further studies are needed to evaluate PD-L1 methylation as a biomarker for response prediction of immunotherapies targeting the PD-1/PD-L1 axis.Entities:
Keywords: CD274; DNA methylation; PD-L1; colorectal cancer; immunotherapeutic; immunotherapies; immunotherapy; microsatellite instability; prognostic biomarker
Year: 2016 PMID: 28197377 PMCID: PMC5283627 DOI: 10.1080/2162402X.2016.1257454
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110