Overview

This trial is active, not recruiting.

Condition colorectal cancer
Treatments oxaliplatin, folinic acid, 5-fluoro-uracil, irinotecan, bevacizumab, cetuximab
Phase phase 2
Targets EGFR, VEGF
Sponsor UNICANCER
Start date December 2010
End date October 2015
Trial size 132 participants
Trial identifier NCT01442649, PRODIGE 18 / ACCORD 22/0906

Summary

The main objective is to evaluate progression-free survival (PFS) at 4 months.

The secondary objectives are to evaluate the objective response rate (OR) (= complete responses (CR) and partial responses (PR)) according to the RECIST v1.1 criteria, the progression-free survival (PFS), the overall survival (OS), the overall survival from the date of the first-line chemotherapy used on the metastatic disease, the treatment tolerance (NCI CTC AE V4 criteria, except for peripheral neurological toxicity (Lévi Scale)), the quality of life according to the EORTC QLQ-C30 criteria.

The objectives of the biological study are to evaluate potentially predictive anti-EGFR and anti-VEGF response factors and CEC rates as predictive biomarkers for the efficacy of bevacizumab associated with chemotherapy in mCRC treatment.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
Every 2 weeks : - mFOLFOX6 : Oxaliplatin 85 mg/m2 over 120 mn IV on D1, Folinic Acide 400 mg/m² (racemic) (or 200 mg/m² if L-folinic acid) over 2 h IV on D1, 5-fluoro-uracil 400 mg/m² in bolus IV on D1 and 5-fluoro-uracil 2400 mg/m² in infusion IV over 46 h. OR - FOLFIRI : Irinotecan 180 mg/m2 en 90 mn IV on day D1, Folinic acid 400 mg/m² (racemic) (or 200 mg/m² if L-folinic acid) over 2 h IV on D1, 5-fluoro-uracil 400 mg/m² in bolus IV on D1 and 5-fluoro-uracil 2400 mg/m² in infusion IV over 46 h. AND Bevacizumab 5 mg/kg IV every 2 weeks.
oxaliplatin
85mg/m² over 120 mn on D1 every 2 weeks up to progression or toxicity
folinic acid
400 mg/m² (racemic) (or 200 mg/m² if L-folinic acid) over 2 h IV on D1 (in the same time that oxaliplatin or irinotecan) every 2 weeks up to progression or toxicity
5-fluoro-uracil
400mg/m² in bolus on D1, then 2400mg/m² over 46 h every 2 weeks up to progression or toxicity
irinotecan
180 mg/m2 over 90 mn IV on D1 every 2 weeks up to progression or toxicity
bevacizumab
5 mg/kg IV over 90 mn on D1 every 2 weeks up to progression or toxicity
(Experimental)
Every 2 weeks : - mFOLFOX6 : Oxaliplatin 85 mg/m2 over 120 mn IV on D1, Folinic Acide 400 mg/m² (racemic) (or 200 mg/m² if L-folinic acid) over 2 h IV on D1, 5-fluoro-uracil 400 mg/m² in bolus IV on D1 and 5-fluoro-uracil 2400 mg/m² in infusion IV over 46 h. OR - FOLFIRI : Irinotecan 180 mg/m2 en 90 mn IV on day D1, Folinic acid 400 mg/m² (racemic) (or 200 mg/m² if L-folinic acid) over 2 h IV on D1, 5-fluoro-uracil 400 mg/m² in bolus IV on D1 and 5-fluoro-uracil 2400 mg/m² in infusion IV over 46 h. AND Cetuximab : 500 mg/m² IV every 2 weeks
oxaliplatin
85mg/m² over 120 mn on D1 every 2 weeks up to progression or toxicity
folinic acid
400 mg/m² (racemic) (or 200 mg/m² if L-folinic acid) over 2 h IV on D1 (in the same time that oxaliplatin or irinotecan) every 2 weeks up to progression or toxicity
5-fluoro-uracil
400mg/m² in bolus on D1, then 2400mg/m² over 46 h every 2 weeks up to progression or toxicity
irinotecan
180 mg/m2 over 90 mn IV on D1 every 2 weeks up to progression or toxicity
cetuximab
500mg/m² on D1 every 2 weeks up to progression or toxicity

Primary Outcomes

Measure
Progression-free survival (PFS) at 4 months
time frame: 4 months

Secondary Outcomes

Measure
Objective response rate (OR)
time frame: 12 months
Progression-free survival (PFS)
time frame: 4 months
Overall survival (OS)
time frame: until death or progression (24 months)
Overall survival from the date of the first-line chemotherapy used on the metastatic disease
time frame: until death or progression (24 months)
Treatment tolerance
time frame: Every 2 weeks, during the treatment.
Quality of life
time frame: every 6 weeks

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: - Histologically or cytologically proven adenocarcinoma of the colon expressing non-mutated (wild-type) KRAS. - Progressive metastatic disease after first-line treatment with chemotherapy alone: based on 5-FU (iv or per os) with irinotecan or oxaliplatin associated to bevacizumab. - Prior adjuvant chemotherapy (of the primary tumor) with fluoropyrimidine and oxaliplatin is allowed if the time interval between the end of this chemotherapy and the beginning of the first-line metastatic treatment is ≥ 6 months. - Measurable disease (at least one measurable metastatic lesion) according to the RECIST V1.1 criteria (the lesion should not be located in a previous field of radiation). - Previous radiotherapy is authorized if discontinued ≥ 15 days prior to randomization and if the measurable metastatic lesions are outside the radiation area. - Sites of disease evaluated within 28 days prior to randomization with thoracic-abdominal-pelvic CT scan (or abdominal-pelvic MRI plus Chest Xray) - Age ≥18 years - Patient with ECOG 0 or 1 - Life Expectancy ≥ 3 months - Hematologic function (polynuclear neutrophiles ≥ 1.5.109/L ; platelets ≥ 100.109/L ; hemoglobin ≥ 9 g/dL - Hepatic transaminases ≤ 2.5 times upper limit of normal (ULN) (≤ 5 ULN in case of hepatic metastases), alkaline phosphatases ≤ 2.5 ULN (≤ 5 ULN in case of hepatic metastases), total bilirubinemia ≤ 1.5 ULN - Renal function (creatinemia ≤1.5 ULN; creatine clearance ≥ 50 mL/mn (Cockcroft and Gault) ; urine test strip < 2+. If proteinuria is ≥ +2 at inclusion, the serum urea test must be redone and show proteinuria ≤ 1 g/L within 24 h) - Completion of the EORTC QLQ-C30 quality of life form - Negative pregnancy test for women of child-bearing age - Information given to the patient and signed informed consent - Public Health insurance coverage Exclusion Criteria: - Known meningeal or brain metastases - Pre-treatment with anti-EGFR - Specific contraindication or known hypersensitivity to one treatment product - Patient with known allergy or hypersensitivity to monoclonal antibodies (bevacizumab, cetuximab - Clinically significant affection of the coronaries or myocardial infarction within 6 months prior to inclusion. - Peripheral neuropathy of grade > 1 (CTCAE scale version 4.0). - Known depletion of the dihydropyrimidine dehydrogenase (DPD). - Acute intestinal obstruction or sub-obstruction, history of inflammatory intestinal disease or extended resection of the small intestine. Presence of a colic prosthesis. - Uncontrolled Arterial hypertension (systolic pressure > 150 mmHg and/or diastolic pressure > 100 mmHg with and without antihypertensive medication. Patients with high hypertension are eligible if antihypertensive medication lowers their arterial pressure to the level of acceptability specified by the inclusion criteria. - History of hypertensive crisis or hypertensive encephalopathy - Other concomitant malignancy or history cancer (except carcinoma in situ of the cervix, or non melanoma skin cancer, with curative intent treatment, when considered in complete remission for at least 5 years before randomization. - Any treatment including an experimental drug, or participation in another clinical trial within 28 days preceding inclusion. - Persons deprived of liberty or under guardianship. - Psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule.

Additional Information

Official title Phase II, Multicentric Randomized Trial, Evaluating the Efficacy of Fluoropyrimidine-based Standard Chemotherapy, Associated to Either Cetuximab or Bevacizumab, in KRAS Wild-type Metastatic Colorectal Cancer Patients With Progressive Disease After Receiving First-line Treatment With Bevacizumab
Principal investigator Jaafar BENNOUNA, Dr
Trial information was received from ClinicalTrials.gov and was last updated in June 2016.
Information provided to ClinicalTrials.gov by UNICANCER.