Hepatic Arterial Infusion With Floxuridine and Systemic Irinotecan After Surgery in Treating Patients With Hepatic (Liver) Metastases From Colorectal Cancer

You may be eligible if

• DISEASE CHARACTERISTICS:
• Histologically confirmed metastatic colorectal adenocarcinoma
• * Primary colorectal adenocarcinoma that has been completely resected (R0 disease)
• * No evidence of residual, viable tumor by abdominal/pelvic helical CT scan or MRI with IV contrast
• * Metastatic disease
• * No more than 9 liver metastases
• * All lesions completely resected or completely treated by ablation (with or without resection)
• * All lesions treated by ablation must have been less than 5 cm in size and at least 5 mm away from main/left/right portal vein, common bile duct, and inferior vena cava
• * All resected lesions must have a negative surgical margin (R0)
• Disease progression after prior systemic irinotecan for metastatic disease allowed
• No extrahepatic metastases confirmed by chest CT scan except colorectal mesenteric lymph node metastases resected at the time of primary tumor resection
• * No other prior resection of extrahepatic metastases
• Must have the entire liver remnant perfused with a single catheter
• Must have a nuclear medicine macro-aggregated albumin flow scan to confirm the area of pump perfusion before study registration
• PATIENT CHARACTERISTICS:
• Age
• 18 and over
• Performance status
• ECOG 0-2 OR
• Zubrod 0-2
• Life expectancy
• Not specified
• Hematopoietic
• WBC at least 3,000/mm\^3
• Absolute granulocyte count at least 1,500/mm\^3
• Absolute neutrophil count at least 1,500/mm\^3
• Platelet count at least 100,000/mm\^3
• Hepatic
• Bilirubin no greater than 2 mg/dL
• Alkaline phosphatase no greater than 2.0 times upper limit of normal (ULN)
• AST and ALT no greater than 2.0 times ULN
• No active hepatitis B or C infection
• No histological evidence of cirrhosis
• Renal
• Creatinine no greater than 1.5 times ULN
• Calcium less than 1.3 times ULN
• Other
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• * Postmenopausal women must be amenorrheic for at least 12 consecutive months to be deemed not fertile
• Medically fit to begin chemotherapy between 4 and 8 weeks after surgery
• Prior cancer allowed if all of the following criteria are met:
• * Undergone potentially curative therapy for all prior malignancies
• * No other malignancy within the past 5 years except the following:
• * Effectively treated basal cell or squamous cell skin cancer
• * Carcinoma in situ of the cervix that has been effectively treated by surgery alone
• * Lobular carcinoma in situ of the ipsilateral or contralateral breast treated by surgery alone
• * No evidence of recurrence of any prior malignancy
• No prior hepatic arterial infusion pump malfunction, malperfusion, or infection
• PRIOR CONCURRENT THERAPY:
• Biologic therapy
• No concurrent immunologic or biologic therapy
• Chemotherapy
• No prior chemotherapy within 4 weeks before hepatic resection or hepatic ablation (with or without resection)
• No prior hepatic arterial infusion with fluorouracil or floxuridine
• Radiotherapy
• No concurrent adjuvant radiotherapy to the pelvis
• No other concurrent radiotherapy
• Other
• No other concurrent systemic therapy