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ABSTRACT: Purpose
Despite expanding options for systemic treatment, survival for metastatic colorectal cancer (mCRC) remains limited and individual response is difficult to predict. In search of pre-treatment predictors, pharmacogenetic research has mainly used a candidate gene approach. Genome wide association (GWA) studies offer the benefit of simultaneously analyzing a large number of SNPs, in both known and still unidentified functional regions. Using a GWA approach, we searched for genetic markers affecting progression free survival (PFS) in mCRC patients treated with first-line capecitabine, oxaliplatin and bevacizumab (CAPOX-B), with or without cetuximab.Patients and methods
755 patients were included in the CAIRO2-trial, a multicenter phase III trial, randomizing between firs
SUBMITTER: Pander J
PROVIDER: S-EPMC4519298 | biostudies-literature | 2015
REPOSITORIES: biostudies-literature