Journal
PHARMACOGENOMICS
Volume 12, Issue 1, Pages 27-39Publisher
FUTURE MEDICINE LTD
DOI: 10.2217/PGS.10.163
Keywords
colorectal cancer; estrogen receptor beta; gender; oxaliplatin; polymorphism
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Funding
- San Pedro Guild [K24CA8275401, P30CA14089]
- NATIONAL CANCER INSTITUTE [P30CA014089, K24CA082754] Funding Source: NIH RePORTER
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Aims: Survival and response rates in metastatic colorectal cancer remain poor, despite advances in drug development. There is increasing evidence to suggest that gender-specific differences may contribute to poor clinical outcome. We tested the hypothesis that genomic profiling of metastatic colorectal cancer is dependent on gender. Materials & methods: A total of 152 patients with metastatic colorectal cancer who were treated with oxaliplatin and continuous infusion 5-fluorouracil were genotyped for 21 polymorphisms in 13 cancer-related genes by PCR. Classification and regression tree analysis tested for gender-related association of polymorphisms with overall survival, progression-free survival and tumor response. Results: Classification and regression tree analysis of all polymorphisms, age and race resulted in gender-specific predictors of overall survival, progression-free survival and tumor response. Polymorphisms in the following genes were associated with gender-specific clinical outcome: estrogen receptor beta, EGF receptor, xeroderma pigmentosum group D, voltage-gated sodium channel and phospholipase A2. Conclusion: Genetic profiling to predict the clinical outcome of patients with metastatic colorectal cancer may depend on gender.
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