Transcatheter arterial embolization followed by octreotide and celecoxib synergistically prolongs survival of rabbits with hepatic VX2 allografts

J Dig Dis. 2013 Jan;14(1):29-37. doi: 10.1111/1751-2980.12001.

Abstract

Objective: To validate the efficacy of an innovative multimodality therapy with transcatheter arterial embolization (TAE) plus octreotide and celecoxib in reducing neoangiogenesis and prolonging the survival of rabbits with hepatocellular carcinoma.

Methods: Rabbits with hepatic VX2 allografts were divided into four groups: control group, TAE group, octreotide + celecoxib (O + C) group and the multimodality therapy (TAE + O + C) group. Survival of the rabbits was analyzed using the Kaplan-Meier method and the expression of CD31 in tumor tissues was detected by immunohistochemistry.

Results: Rabbits in the TAE + O + C group lived nearly 20 days longer than those in the control group. The survival rate of the TAE + O + C group was 50% at day 80 and was the highest among the four groups (P < 0.05). No VX2 allograft-bearing rabbits in the control group lived longer than 60 days. Compared with the control group, the survival time of the other two intervention groups were not prolonged significantly (P > 0.05). The CD31 expression induced by TAE was reduced significantly in TAE + O + C group (P < 0.05). Less metastasis was detected in TAE + O + C group.

Conclusion: TAE followed by the long-term administration of octreotide and celecoxib can synergistically prolong the survival of rabbits with hepatic VX2 allografts by inhibiting potential neoangiogenesis, tumor growth and metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Neoplasms / secondary
  • Analysis of Variance
  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Carcinoma, Hepatocellular / blood supply
  • Carcinoma, Hepatocellular / secondary
  • Carcinoma, Hepatocellular / therapy*
  • Celecoxib
  • Embolization, Therapeutic* / adverse effects
  • Kaplan-Meier Estimate
  • Liver Neoplasms, Experimental / blood supply
  • Liver Neoplasms, Experimental / pathology
  • Liver Neoplasms, Experimental / therapy*
  • Lung Neoplasms / secondary
  • Male
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / pathology
  • Octreotide / administration & dosage
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism
  • Pyrazoles / administration & dosage
  • Rabbits
  • Sulfonamides / administration & dosage
  • Survival Rate

Substances

  • Platelet Endothelial Cell Adhesion Molecule-1
  • Pyrazoles
  • Sulfonamides
  • Celecoxib
  • Octreotide