Combination Chemotherapy With or Without Cetuximab in Treating Patients With Stage III Colon Cancer That Was Completely Removed By Surgery

Federation Francophone de Cancerologie Digestive

Status and phase: Completed; Phase 3

Conditions: Colorectal Cancer

Treatments: Drug: Cetuximab; Drug: Folfox

Study type: Interventional

Funder types: Other

Identifiers

NCT00265811

PETACC-8

EU-20547

MERCK-FFCD-PETACC-8

FFCD-PETACC-8 (Other Identifier)

CDR0000453839

2005-003463-23 (EudraCT Number)

Details and patient eligibility

About

RATIONALE: Drugs used in chemotherapy, such as oxaliplatin, leucovorin, or fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. 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. Cetuximab may also stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving combination chemotherapy with or without cetuximab after surgery may kill any remaining tumor cells and keep colon cancer from coming back. It is not yet known whether giving combination chemotherapy together with cetuximab is more effective than giving combination chemotherapy alone in treating colon cancer.

PURPOSE: This randomized phase III trial is studying combination chemotherapy and cetuximab to see how well they work compared to combination chemotherapy alone in treating patients with stage III colon cancer that was completely removed by surgery.

Full description

OBJECTIVES:

Primary

• Compare the disease-free survival rates in patients with completely resected stage III colon cancer treated with adjuvant oxaliplatin, leucovorin calcium, and fluorouracil with vs without cetuximab.

Secondary

• Compare the 3-year disease-free survival rate and 5-year overall survival rate in patients treated with these regimens.
• Compare the overall survival of patients treated with these regimens.
• Compare the treatment compliance of patients treated with these regimens.
• Determine the prognostic factors and markers predictive for relapse and/or treatment efficacy in patients treated with these regimens.
• Compare the safety of these regimens in these patients.

OUTLINE: This is an open-label, randomized, controlled, multicenter study. Patients are stratified according to obstruction/perforation status (no obstruction and no perforation vs obstruction and/or perforation), N stage (N1 vs N2), and T stage (T1-3 vs T4). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive oxaliplatin IV over 2 hours on day 1 and leucovorin calcium IV over 2 hours and fluorouracil IV continuously over 22 hours on days 1 and 2.
• Arm II: Patients receive chemotherapy as in arm I plus cetuximab IV over 1-2 hours on days 1 and 8.

In both arms, treatment repeats every 14 days for up to 12 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed periodically for approximately 5 years.

PROJECTED ACCRUAL: A total of 2,000 patients will be accrued for this study.

Enrollment: 2,559 patients

Sex: All

Ages: 18 to 74 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed stage III adenocarcinoma of the colon

• Must have undergone curative resection (R0) within the past 28-56 days

  • No radiotherapy prior to surgery

• carcinoembryonic antigen (CEA) ≤ 1.5 times upper limit of normal (ULN) after surgery

• No rectal cancer located within 15 cm from the anal verge by endoscopy or under the peritoneal reflection at surgery

• No metastatic spread at baseline assessment

• No prior or concurrent CNS disease by physical exam

PATIENT CHARACTERISTICS:

Performance status

• WHO 0-1

Life expectancy

• At least 5 years

Hematopoietic

• WBC ≥ 3,000/mm^3
• Absolute neutrophil count ≥ 1,500/mm^3
• Platelet count ≥ 100,000/mm^3
• Hemoglobin ≥ 9 g/dL

Hepatic

• Bilirubin ≤ 1.5 times ULN
• AST and ALT ≤ 2.5 times ULN
• Alkaline phosphatase ≤ 1.5 times ULN

Renal

• Creatinine ≤ 1.5 times ULN

Cardiovascular

• No coronary artery disease
• No myocardial infarction within the past 12 months
• No high risk of uncontrolled arrhythmia

Other

• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No inflammatory bowel disease
• No other malignancy within the past 5 years except basal cell skin cancer or carcinoma in situ of the cervix
• No significant traumatic injury within the past 28 days
• No known hypersensitivity to any of the components of the study drugs
• No medical, geographical, sociological, psychological, or legal condition that would preclude study participation
• No peripheral neuropathy ≥ grade 1
• No other significant disease that would preclude study participation

PRIOR CONCURRENT THERAPY:

Chemotherapy

• No prior chemotherapy

Radiotherapy

• See Disease Characteristics
• No prior abdominal or pelvic irradiation

Surgery

• See Disease Characteristics
• Recovered from prior surgery
• More than 28 days since prior major surgical procedure or open biopsy
• No concurrent major surgical procedure

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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2,559 participants in 2 patient groups

Folfox+Cetuximab

Experimental group

Description:

FOLFOX-4 Cetuximab alone every 2 weeks

Treatment:

Drug: Cetuximab

Drug: Folfox

Folfox

Active Comparator group

Description:

FOLFOX-4 alone every 2 weeks

Treatment:

Drug: Folfox