Annotation Detail

Information
Associated Genes
TP53
Associated Variants
TP53 WILD TYPE
TP53 WILD TYPE
Associated Disease
colorectal cancer
Source Database
CIViC Evidence
Description
In this retrospective biomarker analysis of the EXPERT-C trial, patients with TP53 wild-type status had a statistically significant better progression free survival (PFS) (89.3% vs 65.0% at 5 years; hazard ratio [HR] = 0.23; 95% confidence interval [CI] = 0.07 to 0.78; two-sided P = .02 by Cox regression) and overall survival (OS) (92.7% vs 67.5% at 5 years; HR = 0.16; 95% CI = 0.04 to 0.70; two-sided P = .02 by Cox regression) when treated with Cetuximab + CAPOX (Capecitabine, Oxaliplatin) than in the control arm without Cetuximab.
Variant Origin
N/A
Variant Origin
N/A
Evidence URL
https://civic.genome.wustl.edu/links/evidence_items/875
Gene URL
https://civic.genome.wustl.edu/links/genes/45
Variant URL
https://civic.genome.wustl.edu/links/variants/369
Rating
3
Evidence Type
Predictive
Disease
Colorectal Cancer
Evidence Direction
Supports
Drug
Oxaliplatin,Capecitabine,Cetuximab
Evidence Level
B
Clinical Significance
Sensitivity/Response
Pubmed
24957073
Drugs
Drug NameSensitivitySupported
CapecitabineSensitivitytrue
CetuximabSensitivitytrue
OxaliplatinSensitivitytrue