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CompletedNCT00556413Updated Feb 5, 2026

Cetuximab and Combination Chemotherapy as First-Line Therapy in Treating Patients With Metastatic Colorectal Cancer

A Phase 2 interventional study of cetuximab and fluorouracil in Colorectal Cancer, sponsored by Institut du Cancer de Montpellier - Val d'Aurelle. Completed at 1 site in France. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-02-05.

Sponsored by Institut du Cancer de Montpellier - Val d'Aurelle · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
42
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study 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.

Read the detailed description

OBJECTIVES:

Primary

  • Determine the complete response rate in patients with metastatic colorectal cancer treated with cetuximab and FOLFIRINOX chemotherapy comprising oxaliplatin, irinotecan hydrochloride, leucovorin calcium, and fluorouracil as first-line therapy.

Secondary

  • Determine the objective response rate in patients treated with this regimen.
  • Assess the tolerability of this regimen in these patients.
  • Determine the time to response and time to progression in patients treated with this regimen.
  • Determine the survival of patients treated with this regimen.

OUTLINE: This is a multicenter study.

Patients receive cetuximab IV over 1-2 hours on days 1 and 8. Patients also receive FOLFIRINOX chemotherapy comprising oxaliplatin IV over 2 hours, irinotecan hydrochloride IV over 30-90 minutes, and leucovorin calcium IV over 2 hours on day 1 and fluorouracil IV continuously over 46 hours on days 1 and 2. Treatment repeats every 15 days for up to 12 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 3 months.

02

Conditions studied

  • Colorectal Cancer

Keywords

  • stage IV colon cancer
  • stage IV rectal cancer
  • recurrent colon cancer
  • recurrent rectal cancer
03

In context

Colorectal Neoplasms

5,599 studies on the registry are indexed under Colorectal Neoplasms; 1,459 are open to participants now.

This study's enrollment of 42 is below the median of 77 across 4,123 interventional studies indexed under Colorectal Neoplasms.

Browse Colorectal Neoplasms studies →

Lead sponsor

Institut du Cancer de Montpellier - Val d'Aurelle is the lead sponsor of 138 studies on the registry; 47 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility 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)
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Enrollment
42 participants (actual)

Study arms

  • Experimental
    ERBIRINOX

    5FU + Irinotecan + Oxaliplatine + Cetuximab

    Biological: cetuximab · Drug: fluorouracil · Drug: irinotecan hydrochloride · Drug: leucovorin calcium · Drug: oxaliplatin

Interventions

  • Biologicalcetuximab
  • Drugfluorouracil
  • Drugirinotecan hydrochloride
  • Drugleucovorin calcium
  • Drugoxaliplatin
06

What researchers measure

Primary outcomes

  1. Complete response rate

    Time frame: 6 months

Secondary outcomes

  1. Objective response rate

    Time frame: 6 months

  2. Adverse events by using NCI-CTC

    Time frame: 6 months

  3. Time to response

    Time frame: 6 months

  4. Time to progression

    Time frame: 6 months

  5. Survival

    Time frame: 6 months

07

Study locations

1 site
  • Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle
    Montpellier, 34298, France
08

References and documents

Publications

  • Assenat E, Desseigne F, Thezenas S, Viret F, Mineur L, Kramar A, Samalin E, Portales F, Bibeau F, Crapez-Lopez E, Bleuse JP, Ychou M. Cetuximab plus FOLFIRINOX (ERBIRINOX) as first-line treatment for unresectable metastatic colorectal cancer: a phase II trial. Oncologist. 2011;16(11):1557-64. doi: 10.1634/theoncologist.2011-0141. Epub 2011 Oct 20. PubMed 22016477 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00556413
Lead sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
Responsible party
Sponsor
First posted
Nov 12, 2007
Start date
Sep 2005
Primary completion
May 2011
Completion
Nov 17, 2011
Last update
Feb 5, 2026

Study contacts

Marc Ychou, MD, PhD
study chair · Institut du Cancer de Montpellier - Val d'Aurelle

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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