TY - JOUR
T1 - Oxaliplatin hepatic arterial infusion chemotherapy for hepatic metastases from colorectal cancer
T2 - A phase I-II clinical study
AU - Fiorentini, Giammaria
AU - Rossi, Susanna
AU - Dentico, Patrizia
AU - Meucci, Francesco
AU - Bonechi, Francesco
AU - Bernardeschi, Paolo
AU - Cantore, Maurizio
AU - Guadagni, Stefano
AU - De Simone, Michele
PY - 2004/5
Y1 - 2004/5
N2 - Oxaliplatin is a new drug active in the treatment of advanced colorectal cancer. Hepatic arterial infusion chemotherapy is under evaluation because of the high target dose and low general toxicity. Twelve patients with liver metastases from colorectal cancer were enrolled, all pretreated with evidence of progressive disease: three after a partial remission induced by oxaliplatin, folinic acid and 5-FU, three patients after a partial remission induced by irinotecan, folinic acid and 5-FU and six patients after failing a 5-FU and folinic acid regimen. They received hepatic arterial infusion chemotherapy with oxaliplatin as 30-min infusion on an out-patient basis every 3 weeks. Dose-limiting toxicity was observed at 175 mg/m 2/cycle and consisted of obliteration of the hepatic artery in one patient, abdominal pain requiring morphine in one patient and severe hypotension requiring plasma expander in a third. Following phase I, all patients received 150 mg/m 2 for six cycles. We reported four cases of partial remission (33%) lasting 24, 15, 12 and 10+ weeks, respectively, 2 stabilisation of disease (17%) lasting more than 12 weeks and six progressions (50%). Six patients (50%) presented CEA reduction of >30% and five patients (41%) showed an increase of >8% of body weight. The median survival was 13 months (range 6-19). Oxaliplatin did not present significant toxicity for liver parenchyma and biliary tree. We advise that further studies be undertaken with oxaliplatin 150 mg/m 2.
AB - Oxaliplatin is a new drug active in the treatment of advanced colorectal cancer. Hepatic arterial infusion chemotherapy is under evaluation because of the high target dose and low general toxicity. Twelve patients with liver metastases from colorectal cancer were enrolled, all pretreated with evidence of progressive disease: three after a partial remission induced by oxaliplatin, folinic acid and 5-FU, three patients after a partial remission induced by irinotecan, folinic acid and 5-FU and six patients after failing a 5-FU and folinic acid regimen. They received hepatic arterial infusion chemotherapy with oxaliplatin as 30-min infusion on an out-patient basis every 3 weeks. Dose-limiting toxicity was observed at 175 mg/m 2/cycle and consisted of obliteration of the hepatic artery in one patient, abdominal pain requiring morphine in one patient and severe hypotension requiring plasma expander in a third. Following phase I, all patients received 150 mg/m 2 for six cycles. We reported four cases of partial remission (33%) lasting 24, 15, 12 and 10+ weeks, respectively, 2 stabilisation of disease (17%) lasting more than 12 weeks and six progressions (50%). Six patients (50%) presented CEA reduction of >30% and five patients (41%) showed an increase of >8% of body weight. The median survival was 13 months (range 6-19). Oxaliplatin did not present significant toxicity for liver parenchyma and biliary tree. We advise that further studies be undertaken with oxaliplatin 150 mg/m 2.
KW - Hepatic arterial infusion chemotherapy
KW - Liver metastases from colorectal cancer
KW - Oxaliplatin
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M3 - Article
C2 - 15274406
AN - SCOPUS:3242679883
SN - 0250-7005
VL - 24
SP - 2093
EP - 2096
JO - Anticancer Research
JF - Anticancer Research
IS - 3 B
ER -