Leucovorin, Fluorouracil, Cetuximab, and Oxaliplatin in Treating Patients With Stage IV Colorectal Cancer and Liver Metastases That Cannot Be Removed by Surgery

NCT ID: NCT00544349

Last Updated: 2011-05-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 45 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-10-31

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as leucovorin, fluorouracil, and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. 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. Giving more than one drug (combination chemotherapy) and giving them together with cetuximab may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving leucovorin together with fluorouracil, cetuximab, and oxaliplatin works in treating patients with stage IV colorectal cancer and liver metastases that cannot be removed by surgery.

Detailed Description

OBJECTIVES:

Primary

• Determine the efficacy of this regimen by the measurement of objective response rate (RECIST criteria).

Secondary

• Determine the toxicity of this regimen.
• Evaluate the duration of tumor response.
• Determine the duration and rate of tumor control.
• Determine the rate of secondary resectability of hepatic metastases.
• Evaluate progression-free survival
• Determine rate of progression of the tumor.
• Determine overall survival.

OUTLINE: This is a multicenter study.

Patients receive cetuximab IV over 1 hour, leucovorin calcium IV over 2 hours, and fluorouracil IV continuously over 46 hours. Patients also receive oxaliplatin by hepatic arterial infusion over 2 hours. Treatment continues for at least 3 months in the absence of disease progression or unacceptable toxicity.

Conditions

Colorectal Cancer; Metastatic Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

cetuximab

Intervention Type: BIOLOGICAL

fluorouracil

Intervention Type: DRUG

leucovorin calcium

Intervention Type: DRUG

oxaliplatin

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• WHO performance status 0-1
• Life expectancy > 3 months
• ANC ≥ 1,500/mm³
• Platelet count ≥ 100,000/mm³
• Hemoglobin ≥ 9 g/dL
• Creatinine ≤ 1.5 times normal
• Bilirubin ≤ 1.5 times upper limit of normal
• Transaminases ≤ 5 times normal
• Not pregnant or nursing
• Fertile patients must use effective contraception

Exclusion Criteria

• Contraindication or allergy grade 3-4 to any components of the study drugs
• Peripheral neuropathy
• Intestinal occlusion or subocclusion or prior inflammatory intestinal disease
• Severe cardiac disease including any of the following:

• Symptomatic coronary disease
• Myocardial infarction in the past 6 months
• New York Heart Association grade II-IV cardiac insufficiency
• Severe arrhythmia (even if treated)
• Active or uncontrolled infection
• Other concurrent serious disorder
• Severe uncontrolled medical condition
• Other malignancy within the past 5 years or concurrently except basal cell skin cancer or carcinoma in situ of the cervix
• Study impossible due to psychological, geographical, or social reasons
• Prisoners or patients under guardianship

PRIOR CONCURRENT THERAPY:

• Prior chemotherapy except adjuvant chemotherapy comprising fluorouracil, leucovorin calcium, capecitabine, oxaliplatin, irinotecan hydrochloride, and/or bevacizumab (completed > 6 months ago if oxaliplatin- or irinotecan-based)
• Prior epidermal growth factor (EGF), monoclonal antibody inhibiting transduction of EGF receptor (EGFR), or any other treatment targeting the EGFR
• Other concurrent anticancer immunotherapy, chemotherapy, or hormone therapy
• Participation in another study in the past 30 days

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Gustave Roussy, Cancer Campus, Grand Paris

OTHER

Sponsor Role: lead

Principal Investigators

David Malka, MD, PhD

Role:

Gustave Roussy, Cancer Campus, Grand Paris

Locations

Hopital Saint Andre

Bordeaux, , France

Centre Regional Francois Baclesse

Caen, , France

Centre de Lutte Contre le Cancer Georges-Francois Leclerc

Dijon, , France

CHU Pitie-Salpetriere

Paris, , France

Centre Eugene Marquis

Rennes, , France

Hopital Paul Brousse

Villejuif, , France

Institut Gustave Roussy

Villejuif, , France

Countries

France

Other Identifiers

FRE-IGR-CHOICE

Identifier Type: -

Identifier Source: secondary_id

IGR-1207

Identifier Type: -

Identifier Source: secondary_id

INCA-RECF0449

Identifier Type: -

Identifier Source: secondary_id

CDR0000564063

Identifier Type: -

Identifier Source: org_study_id