Colorectal Cancer
Conditions
Brief summary
To assess the efficacy of FOLFOX4 in combination with cetuximab, weekly and FOLFOX4 in combination with cetuximab, biweekly.
Detailed description
This multicenter randomized phase II study will enroll approximately 150 patients with metastatic Colorectal Cancer. Patients are randomized in Arm A(FOLFOX4 in combination with weekly Cetuximab) or Arm B (FOLFOX4 in combination with biweekly Cetuximab). Both efficacy and safety data will be collected. The investigator will assess response to treatment every 8 weeks based on the imaging. Following permanent treatment cessation, patients will be followed-up for survival.
Interventions
DRUGFOLFOX4 (Oxaliplatin), Cetuximab
Arm A FOLFOX4: * Oxaliplatin 85 mg/m² d1 * Leucovorin 200 mg/m² d1+d2, followed by * Bolus 5FU 400 mg/m², followed by * Infusional 5FU 600 mg/m²,over 22 hours, every 2 weeks Cetuximab is administered to arm A of the study as an infusion with initial dose 400 mg/m² in week 1 followed by weekly doses of 250 mg/m². Arm B FOLFOX4: * Oxaliplatin 85 mg/m² d1 * Leucovorin 200 mg/m² d1+d2, followed by * Bolus 5FU 400 mg/m² , followed by * Infusional 5FU 600 mg/m², over 22 hours, every 2 weeks Cetuximab is administered to arm B of the study as infusions of 500 mg/m² every two weeks.
Sponsors
Central European Cooperative Oncology Group
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Signed written informed consent * Male or female ≥ 18 years of age * Diagnosis of histologically confirmed adenocarcinoma of the colon or rectum * Metastatic colorectal carcinoma not suitable for curative-intent resection- Availability of tumor sample (or able and willing to provide tumor sample) for EGFR assessment * Presence of at least one lesion measurable unidimensionally by CT scan or MRI. (Target lesion(s) must not lie within an irradiated area) * Karnofsky performance status of \> 80 at study entry * Leucocytes ≥ 3.0 x 10 9/L and neutrophils ≥1.5 x 10 9/L, platelets ≥ 100 x 10 9/L, and hemoglobin ≥ 9 g/dL. * Bilirubin ≥ 1.5 x ULN * ASAT and ALAT ≤ 2.5 x ULN (≤5 x ULN if liver metastasis are present) * Serum creatinine ≤ 1.5 x ULN
Exclusion criteria
* Brain metastasis (known or suspected) * Previous chemotherapy for metastatic disease. Prior adjuvant chemotherapy is allowed if the chemotherapy treatment free interval is \> 6 months. * Surgery (excluding diagnostic biopsy) or irradiation within 4 weeks prior to study entry * Concurrent chronic systemic immune therapy, chemotherapy, or hormone therapy not indicated in the study protocol * Any investigational agent(s) within 4 weeks prior to entry * Previous exposure to EGFR-pathway targeting therapy * Clinically relevant coronary artery disease or a history of a myocardial infarction within the last 12 months * Acute or subacute intestinal occlusion or history of inflammatory bowel disease * Pre-existing neuropathy \> grade 1. In case of prior oxaliplatin containing adjuvant chemotherapy: pre-existing neuropathy ≥ 1. * Known grade 3 or 4 allergic reaction to any of the components of the treatment. * Any concurrent malignancy other than non-melanoma skin cancer, or carcinoma in situ of the cervix. (Patients with a previous malignancy but without evidence of disease for ≥ 5 years will be allowed to enter the trial) * Pregnancy or lactation * Inadequate contraception (male or female patients) if of childbearing or procreational potential * Known drug abuse/ alcohol abuse * Legal incapacity or limited legal capacity * Medical or psychological condition which in the opinion of the investigator would not permit the patient to complete the study or sign meaningful informed consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The primary endpoint of the trial is: • Objective response (CR/PR), as assessed by RECIST criteria | The objective response rate - defined as the rate of subjects with complete response (CR) or partial response (PR) | Objective response (partial or complete) will be assessed using RECIST criteria. The objective response rate (defined as the rate of subjects with complete response (CR) or partial response (PR)) will be estimated and associated exact two-sided 95% confidence limit (Clopper-Pearson) will be calculated. In addition to the estimates within each treatment group odds ratios and associated 95% CI will be calculated using the Cochran Mantel-Haenszel procedure. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| • Progression Free Survival (PFS) • Overall survival • Safety/Adverse events Safety | he rate of subjects with complete response (CR) or partial response (PR) | Secondary objectives are the estimation of differences in PFS and overall survival. |
Countries
Austria, Bosnia and Herzegovina, Bulgaria, Croatia, Estonia, Greece, Hungary, Israel, Latvia, Romania, Serbia, Slovakia, Slovenia
Outcome results
None listed