Study of Oxaliplatin, Capecitabine and Bevacizumab as First Line Treatment for Patients With Advanced Colorectal Cancer

Inclusion Criteria:

Histologically or cytologically confirmed metastatic or recurrent colorectal tumors with no previous treatment for advanced disease.
Age greater than or equal to 18 years
SWOG performance status 0-1.
At least one measurable lesion according to the RECIST criteria which has not been irradiated (i.e. newly arising lesions in previously irradiated areas are accepted). Minimum indicator lesion size: > 10 mm measured by spiral CT or >20mm measured by conventional techniques.
Have a negative serum pregnancy test within 7 days prior to initiation of chemotherapy (female patients of childbearing potential).
Availability of tumor biopsy (paraffin embedded or fresh frozen) at the time of diagnosis and/or prior to study entry is required.
Patients must agree to have a 20 cc blood sample drawn in addition to routine labs with each cycle of chemotherapy.

Exclusion Criteria:

Pregnant or lactating woman.
Life expectancy < 3 months.
Serious, uncontrolled, concurrent infection(s) or illness(es)
Any prior oxaliplatin treatment, with the exception of adjuvant therapy given > 12 months prior to the beginning of study therapy
Prior unanticipated severe reaction to fluoropyrimidine therapy, known hypersensitivity to 5-fluorouracil, or known DPD deficiency
Prior unanticipated severe reaction or hypersensitivity to platinum based compounds.
Treatment for other carcinomas within the last five years, except cured non-melanoma skin and treated in-situ cervical cancer.
Current, recent (within 4 weeks of first infusion on this study) or planned participation in an investigational drug study.
Clinically significant cardiac disease (e.g. congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmias not well controlled with medication) within the last 6 months.
History of clinically significant interstitial lung disease and/or pulmonary fibrosis.
History of persistent neurosensory disorder including but not limited to peripheral neuropathy.
Presence of central nervous system or brain mets.
Major surgery, open biopsy, or significant traumatic injury within 28 days prior to Day 0, or anticipation of need for major surgical procedure during the course of the study.
Lack of physical integrity of the upper gastrointestinal tract or malabsorption syndrome.

Any of the following laboratory values:

Abnormal hematologic values (neutrophils < 1.5 x 109/L, platelet count < 100 x 109/L)
Urine protein: creatinine ratio >/= 1.0 Impaired renal function with estimated creatinine clearance < 30 ml/min as calculated with Cockroft et Gault equation:
Serum bilirubin > 1.5 x upper normal limit. ALT, AST > 2.5 x upper normal limit (or > 5 x upper normal limit in the case of liver metastases)
Alkaline phosphatase > 2.5 x upper normal limit (or > 5 x upper normal limit in the case of liver metastases or > 10 x upper normal limit in the case of bone disease)
Minor surgical procedures, fine needle aspirations or core biopsies within 7 days prior to Day 0
Blood pressure > 150/100 mmHg
Unstable angina
New York Heart Association (NYHA) Grade II or greater congestive heart failure
History of myocardial infarction or stroke within 6 months
Clinically significant peripheral vascular disease
Evidence of bleeding diathesis or coagulopathy
History of abdominal fistula, gastrointestinal perforation or intraabdominal abscess within 28 days prior to Day 0.
Serious, non-healing wound, ulcer or bone fracture
Carcinoma of any histology in close proximity to a major vessel, cavitation or history of hemoptysis.
Completion of previous adjuvant chemotherapy regimen < four weeks prior to the start of study treatment (within six weeks of study treatment for mitomycin C and nitroureas), or with related toxicities unresolved prior to the start of study treatment.