TY - JOUR
T1 - Pharmacokinetic advantage of intra-arterial hepatic oxaliplatin administration
T2 - Comparative results with cisplatin using a rabbit VX2 tumor model
AU - Dzodic, Radan
AU - Gomez-Abuin, Gonzalo
AU - Rougier, Philippe
AU - Bonnay, Marc
AU - Ardouin, Patrice
AU - Gouyette, Alain
AU - Rixe, Olivier
AU - Ducreux, Michel
AU - Munck, Jean Nicolas
PY - 2004/7/1
Y1 - 2004/7/1
N2 - The aim of this study was to compare intra-arterial hepatic administration (IAH) versus i.v. administration of oxaliplatin and cisplatin in a VX2 tumor model in rabbits. VX2 tumors were implanted in the livers of White New Zealand female rabbits and 2 weeks later they received either cisplatin (4 mg/kg) or oxaliplatin (6 mg/kg) administered by IAH or i.v. Platinum pharmacokinetic parameters were measured by atomic absorption spectrometry at baseline, 2, 5 10, 20, 40 and 60 min, and then at 2, 4, 6 and 24 h after drug administration. Animals were sacrificed 24 h after drug administration to measure platinum concentrations in various tissues. After IAH oxaliplatin administration, we observed a significant decrease for total and filterable platinum in the C max compared with i.v. administration (12.4 versus 18.2 μg/l; p=0.02 and 11.2 versus 17.3 μg/l; p=0.02, respectively). Significant differences in various tissue concentrations were reported when comparing IAH and i.v. administration of oxaliplatin with IAH administration offering an advantage over i.v. administration. No differences in pharmacokinetic parameters or platinum tissue accumulation were apparent between the IAH and i.v. administration with cisplatin. We conclude that there is a significant pharmacokinetic advantage to using oxaliplatin for locoregional IAH chemotherapy compared with i.v. administration.
AB - The aim of this study was to compare intra-arterial hepatic administration (IAH) versus i.v. administration of oxaliplatin and cisplatin in a VX2 tumor model in rabbits. VX2 tumors were implanted in the livers of White New Zealand female rabbits and 2 weeks later they received either cisplatin (4 mg/kg) or oxaliplatin (6 mg/kg) administered by IAH or i.v. Platinum pharmacokinetic parameters were measured by atomic absorption spectrometry at baseline, 2, 5 10, 20, 40 and 60 min, and then at 2, 4, 6 and 24 h after drug administration. Animals were sacrificed 24 h after drug administration to measure platinum concentrations in various tissues. After IAH oxaliplatin administration, we observed a significant decrease for total and filterable platinum in the C max compared with i.v. administration (12.4 versus 18.2 μg/l; p=0.02 and 11.2 versus 17.3 μg/l; p=0.02, respectively). Significant differences in various tissue concentrations were reported when comparing IAH and i.v. administration of oxaliplatin with IAH administration offering an advantage over i.v. administration. No differences in pharmacokinetic parameters or platinum tissue accumulation were apparent between the IAH and i.v. administration with cisplatin. We conclude that there is a significant pharmacokinetic advantage to using oxaliplatin for locoregional IAH chemotherapy compared with i.v. administration.
KW - Hepatic
KW - Intra-arterial
KW - Oxaliplatin
UR - http://www.scopus.com/inward/record.url?scp=3142708548&partnerID=8YFLogxK
U2 - 10.1097/01.cad.0000131684.06390.fe
DO - 10.1097/01.cad.0000131684.06390.fe
M3 - Article
C2 - 15205611
AN - SCOPUS:3142708548
SN - 0959-4973
VL - 15
SP - 647
EP - 650
JO - Anti-Cancer Drugs
JF - Anti-Cancer Drugs
IS - 6
ER -