Exploratory Study Of The ERCC-1 Gene

Inclusion Criteria:

Histologically confirmed diagnosis of colorectal cancer.
ECOG Performance Status 0-2 (Appendix A).
Patient is a candidate for oxaliplatin based therapy either in the adjuvant or in the metastatic setting.
Consent to donate 4 tubes of PBMC of 7 ml of blood each.
Willing to consider additional post therapy tumor biopsy if applicable (refusal to consent is not an exclusion criteria).

Adequate organ function as defined as:

Neutrophil count > 1500/μl
Platelets > 75,000/ μl
Hemoglobin > 8 g/dl
Bilirubin < 2.0 X upper limit of normal
Creatinine < 2 mg% or calculated clearance > 40 ml/mt
The patient must have signed a consent form approved by the Albert Einstein College of Medicine Cancer Center CCI and Montefiore Medical Center IRB

Exclusion Criteria:

No other significant underlying medical condition that will, in the opinion of the principal investigator or designees, make administration of oxaliplatin unusually hazardous, such as significant hepatic, bone marrow and/or cardiac disease, requiring active medical treatment.
Pregnant women or women of child bearing potential not practicing birth control or sexually active males unwilling to practice contraception during the study.
Patients undergoing major surgical procedures (they will be delayed enrollment until complete recovery from their surgery - 4 wk for major or 2 wk from minor surgery).
Patients with grade 2 neuropathy will not be eligible for the study.
The patient must not have received chemotherapy within 4 weeks of beginning oxaliplatin treatment. At least 6 weeks must elapse if prior therapy included mitomycin C or nitrosoureas. At least 2 weeks must have elapsed since the end of prior palliative radiation therapy.