Combination Chemotherapy in Treating Patients With Colorectal Cancer and Resectable Metastases
- Sponsor
- GERCOR - Multidisciplinary Oncology Cooperative Group
- Study ID
- NCT00268398
- Phase
- PHASE3
- Status
- Completed
Conditions
- Chemotherapy
- Colorectal Cancer
- Metastatic Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- oxaliplatin, folinic acid, fluorouracil — DRUGfolinic acid 200 mg/m² (day 1\&2) oxaliplatin 85 mg/m² (day 1) bolus 5FU 400 mg/m² (day 1\&2) continuous 5FU 600mg/m² (day 1 to 2)
- oxaliplatin, irinotecan, folinic acid, fluorouracil — DRUGFOLFOX7 folinic acid 400 mg/m² (day 1) oxaliplatin 130 mg/m² (day 1) continuous 5FU 3000mg/m² (day 1 to 2) FOLFIRI folinic acid 400 mg/m² (day 1) irinotecan 180 mg/m² (day 1) bolus 5FU 400 mg/m² (day 1) continuous 5FU 2400mg/m² (day 1 to 2)
Study Details
PURPOSE: This randomized phase III trial is studying two different combination chemotherapy regimens to compare how well they work in treating patients with colorectal cancer and resectable metastases.
Key Dates
- Start date
- Jul 31, 2002
- Status verified
- May 2012
- Primary completion
- Dec 31, 2011
Study Design
- Enrollment
- 284 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: FOLFOX4
- Experimental: FOLFOX7 followed by FOLFIRI
Primary Outcome Measure
disease-free survival [ Time Frame: 2-year ]
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