Experimental study on TNF-alpha linked percutaneous isolated hepatic chemoperfusion (PIHP)

Recently, isolated hepatic perfusion (IHP) with high-dose TNF-alpha for hepatic malignancies has again attracted attention as a locoregional chemotherapy. A novel system of hepatic venous isolation and charcoal hemoperfusion (HVI.CHP) is a minimal invasive surgery for high-dose chemotherapy of the l...

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Bibliographic Details
Published inGan to kagaku ryoho Vol. 25; no. 9; p. 1278
Main Authors Kusunoki, N, Ku, Y, Kuroda, Y
Format Journal Article
LanguageJapanese
Published Japan 01.07.1998
Subjects
Animals
Autoantibodies - administration & dosage
Chemotherapy, Cancer, Regional Perfusion - methods
Dogs
Liver Neoplasms - metabolism
Liver Neoplasms - therapy
Recombinant Proteins - administration & dosage
Tumor Necrosis Factor-alpha - administration & dosage
Tumor Necrosis Factor-alpha - immunology
Tumor Necrosis Factor-alpha - pharmacokinetics
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Summary:Recently, isolated hepatic perfusion (IHP) with high-dose TNF-alpha for hepatic malignancies has again attracted attention as a locoregional chemotherapy. A novel system of hepatic venous isolation and charcoal hemoperfusion (HVI.CHP) is a minimal invasive surgery for high-dose chemotherapy of the liver. This study was undertaken to determine whether this novel system could limit systemic exposure to TNF-alpha following hepatic arterial infusion (HAI) when combined with anti TNF-alpha antibody. Beagles were allocated into two groups; group I (n = 4), TNF-alpha + anti TNF-alpha antibody and group II (n = 5), TNF-alpha only (control). All animals received HAI of 50 micrograms/kg of recombinant human TNF-alpha over 20 min with complete hepatic venous isolation. In group I, 250 micrograms/kg of antibody was administered into the hepatic venous outflow line over 30 min after the initiation of HAI. The Cmax (ng/ml) of systemic TNF level was significantly lower in group I (125 +/- 57) than in group II (825 +/- 283) (p < 0.05). The AUC (mg.min/ml) of the systemic TNF level was significantly lower in group I (2.0 +/- 1.0) than in group II (34.5 +/- 9.5) (p < 0.01). By use of anti TNF antibody, systemic exposure to TNF was reduced efficiently. These results indicated that HVI.CHP may be applicable to the TNF-alpha linked chemoperfusion to the liver in combination with anti TNF-alpha antibody.
ISSN:0385-0684