Clinical trial · Interventional
Cetuximab and Combination Chemotherapy as First-Line Therapy in Treating Patients With Metastatic Colorectal Cancer
Phase II Study Evaluating the Efficacy and Safety of cétuximab Associated With the Protocol FOLFIRINOX (LV5FU Simplified Combined With Irinotecan and Oxaliplatin) in the First Line Treatment in Patients With Metastatic Colorectal Cancer Expressing EGFR or Not
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colorectal Cancer | Malignant Colorectal Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (5)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| cetuximab | Biological | Cetuximab | ALIAS |
| fluorouracil | Drug | Fluorouracil | ALIAS |
| irinotecan hydrochloride | Drug | Irinotecan | ALIAS |
| leucovorin calcium | Drug | Leucovorin | ALIAS |
| oxaliplatin | Drug | Oxaliplatin | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- ERBIRINOX
- description
- 5FU + Irinotecan + Oxaliplatine + Cetuximab
- interventionNames
- Biological: cetuximab
- Drug: fluorouracil
- Drug: irinotecan hydrochloride
- Drug: leucovorin calcium
- Drug: oxaliplatin
Primary outcomes (1)
- measure
- Complete response rate
- timeFrame
- 6 months
Secondary outcomes (5)
- measure
- Objective response rate
- timeFrame
- 6 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
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)
References
Publications (1)
- RESULTAssenat 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. PMID 22016477