Colorectal cancer is the 3rd most common cancer in France and the 2nd cause of death from cancer. Between 30 to 60% of patients develop limited or predominant liver metastases. Surgical resection of these metastases, only curative treatment is not immediately possible in 10-15% of cases. In unresectable patients, current palliative treatments are based on systemic chemotherapy associated or not with the targeted therapies (anti-EGFR (panitumumab), anti-VEGF (bevacizumab)). In this patient population, special attention was paid to intensified treatment regimens in order to improve their efficiency and improving the tumoral response rate, the intensity of the response and its earliness correlate with improved overall and progression-free survival. The intra-arterial use of oxaliplatin coupled with IV chemotherapy has yielded OR levels of 64% in patients having survived one or more lines of chemotherapy IV and 62% in patients who have progressed on oxaliplatin IV. In addition, the HIA administration of oxaliplatin limits systemic and especially neurological toxicities, thanks to a greater hepatic clearance. In conclusion, the combination of systemic chemotherapy, targeted therapy and HIAC with oxaliplatin has showed promising efficacy results associated with good tolerance from the first line onwards. Indeed, we can expect from the Phase II recent data, a control rate close to 100%, with high response rates associated with early maturity and depth responses as well as prolonged survival. However, to date, in the absence of randomized trial testing this combination, this strategy does not have sufficient evidence to be integrated in our routine practices, and HIAC remains limited to a few expert centers in treatment catch-up.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
348
85 mg/m² in intravenous. 1 cycle each 15 days
5 fluorouracil : 400 mg/m² in bolus of 10 minutes (intravenous) following by 2400 mg/m² during 46 hours in intravenous
400 mg/m² in intravenous
85 mg/m² in intra-arterial. 1 cycle each 15 days
Only for patient RAS wild: 6 mg/Kg at each cycle in intravenous
5 mg/kg at each cycle in intravenous
2400 mg/m² intravenously over 46 hours
150 mg/m² intravenous
Hôpital Erasme
Brussels, Belgium
RECRUITINGChu Hotel Dieu
Angers, France
RECRUITINGInstitut de Cancérologie de l'Ouest
Angers, France
RECRUITINGHôpital Privé d'Antony
Antony, France
progression-free survival
comparison of radiological/clinical progression free survival
Time frame: 24 months after randomization
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CH Henri Duffaut
Avignon, France
NOT_YET_RECRUITINGInstitut du cancer Avignon Provence
Avignon, France
RECRUITINGCh Cote Basque
Bayonne, France
RECRUITINGClinique Belharra
Bayonne, France
RECRUITINGCentre Hospitalier
Beauvais, France
NOT_YET_RECRUITINGInstitut Bergonié
Bordeaux, France
RECRUITING...and 39 more locations