Safety and Efficacy Study of Combination Therapy With Cetuximab and FOLFOX4 in Patients With Colorectal Cancer

Spanish Cooperative Group for the Treatment of Digestive Tumours (TTD)

Status and phase

Completed

Phase 2

Conditions

Colorectal Cancer

Treatments

Drug: FOLFOX-4+cetuximab

Drug: FOLFOX-4

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00202787

eudract-number: 2004-001700-12

TTD-04-02

Details and patient eligibility

About

The purpose of this study is to determine confirmed objective response rate to combination therapy with cetuximab and FOLFOX4 or FOLFOX4 alone in patients with CRC and non-resectable hepatic metastases

Enrollment

136 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Written informed consent.
Men and women < 75 years
Histologically confirmed diagnosis of CRC
Metastatic colorectal carcinoma with exclusive non-resectable hepatic metastases, due to fulfillment of one of the following criteria:
1. Number of hepatic metastases > or= 4;
2. Size of one or more hepatic metastases > 5 cm diameter;
3. Vascular involvement and/or poor site that prevent complete resection of hepatic disease and/or require resection with the remaining liver mass less than 25-30% of functional liver.
Presence of at least one lesion detectable by two-dimensional measurement.
Karnofsky functional status >or=70% at the time of enrollment in study
Life expectancy greater than 3 months.
Patients must not have received chemotherapy for advanced/metastatic disease.
Patients with the following characteristics will be enrolled:
1. Recurrence after adjuvant treatment with 5-fluorouracil/folinic acid or capecitabine +/- radiotherapy with disease-free period > 6 months following conclusion of treatment.
2. Recurrence after surgical and/or radiotherapy treatment without adjuvant systemic treatment.
3. De novo diagnosis of disease.
Proper liver function, defined by aspartate aminotransferase (AST/SGOT) and alanine aminotransferase (ALT/SGPT) < or = 2.5 x ULN (< or = 5 x ULN if there are hepatic metastases) and total bilirubin count < 1.5 x ULN.
Proper kidney function, defined as serum creatinine < 1.5 x ULN.
Proper hematological function, defined as neutrophil count > or = 1.5 x 109/l , platelets > or = 100 X 109/l and hemoglobin > or = 9 g/dl.
Effective birth control method for men as well as women if there is possibility of pregnancy

Exclusion criteria

Documented or suspected cerebral and/or leptomeningeal metastases.
Metastasis in any other non-hepatic site, including extrahepatic lymph node metastases.
Surgery (excluding biopsy for diagnosis) and/or radiotherapy within 4 weeks prior to enrollment in the study.
Participation in another clinical trial with medication in the past 30 days.
Chronic, concomitant administration of systemic immunotherapy, chemotherapy, hormone therapy or any other investigational drug.
Prior malignant tumour in past 5 years, except history of basal cell skin carcinoma or pre-invasive cervical carcinoma.
Any investigational drug during the 4 weeks prior to enrolment.
Prior administration of monoclonal antibodies, EGFR signal transduction inhibitors or EGFR-targeted treatment.
Prior participation in study in which treatment with cetuximab can be assigned (whether or not treatment with cetuximab is received)
Acute or subacute intestinal occlusion or history of inflammatory intestinal disease.
Evidence of grade 3 or 4 allergic reaction to any of the treatment components.
Clinically relevant peripheral neuropathy.
Clinically relevant myocardial disease or history of myocardial infarction in the past 12 months.
Known abuse of alcohol / drugs, Legal incapacity or limited legal capacity.
Any medical or psychological disorder which, in the opinion of the investigator, does not allow the patient to conclude the study or sign the informed consent.
Pregnant or nursing woman