Overview
Cetuximab and Combination Chemotherapy as First-Line Therapy in Treating Patients With Metastatic Colorectal Cancer
Status:
Completed
Completed
Trial end date:
2011-11-17
2011-11-17
Target enrollment:
0
0
Participant gender:
All
All
Summary
RATIONALE: Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving cetuximab together with combination chemotherapy may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving cetuximab together with combination chemotherapy works as first-line therapy in treating patients with metastatic colorectal cancer.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Institut du Cancer de Montpellier - Val d'AurelleTreatments:
Calcium
Cetuximab
Fluorouracil
Irinotecan
Leucovorin
Levoleucovorin
Oxaliplatin
Criteria
DISEASE CHARACTERISTICS:- Histologically confirmed colorectal cancer
- Metastatic, unresectable disease
- May or may not express the EGFR gene
- Measurable disease, defined as ≥ 1 measurable lesion by MRI or CT scan
- Lesion must be outside an irradiated area
PATIENT CHARACTERISTICS:
- WHO performance status 0-1
- Life expectancy > 3 months
- ANC ≥ 1,500/mm³
- Platelet count ≥ 100,000/mm³
- Hemoglobin ≥ 9 g/dL
- Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
- Transaminases ≤ 2.5 times ULN (5 times ULN if hepatic metastases are present)
- Creatinine ≤ 1.5 times ULN
- Not pregnant or nursing
- Fertile patients must use effective contraception
- No peripheral or symptomatic neuropathy ≥ grade 2 (NCI-CTCAE)
- No complete or partial intestinal blockage
- No intestinal inflammatory disease (e.g., Crohn's disease or ulcerative colitis)
- No chronic diarrhea
- No severe unstable cardiac disease (despite treatment)
- No myocardial infarction within the past 6 months
- No neurological or psychiatric illness, including epilepsy or dementia
- No uncontrolled active infection
- No other prior or concurrent malignancy within the past 5 years except for curatively
treated basal cell skin cancer
- No psychological, familial, social, or geographic reason that would preclude study
follow-up
PRIOR CONCURRENT THERAPY:
- No prior chemotherapy for metastatic disease
- Prior fluorouracil-based adjuvant chemotherapy allowed provided it was
administered ≥ 4 weeks ago
- At least 4 weeks since prior and no other concurrent experimental therapy
- No prior irinotecan hydrochloride, oxaliplatin, or monoclonal antibody
- No prior intestinal resection (e.g., hemicolectomy or extended resection of the small
intestine)