TY - JOUR
T1 - Survival after gamma interferon intratumoral injections in a model of hepatocarcinoma
AU - Peyrègne, Vincent
AU - Quash, Gerard
AU - Isaac, Sylvie
AU - Chantepie, Jacqueline
AU - Akiba, Hitoshi
AU - Scoazec, Jean Yves
AU - Gilly, Francois Noël
PY - 2004/7/1
Y1 - 2004/7/1
N2 - Background/Aims: Short-term efficacy of local gamma interferon delivered via a single injection of an adenovirus-gamma interferon vector has been reported in immunocompetent animals which develop spontaneous liver cancer. However the long-term outcome was not examined. The aim of this randomized trial was to assess in an immunodeficient mouse ectopic model the benefit, if any, of the long-term efficacy of intratumoral injections of gamma interferon itself. Methodology: 77 mice were randomly assigned to 4 groups. Gamma interferon treated groups received a dose of 5000, 10000 or 20000 IU per animal versus phosphate-buffered saline. The follow-up lasted 46 days. Results: Significant differences were noted in mice receiving 20000 IU compared to controls: increase in survival (p=0.0485), slowing down of tumor growth in large tumors (p=0.009), increase in necrosis (p=0.004). The preferential staining in necrotic areas with anti-Class II antibody and the accumulation of nuclear debris indicated that neutrophils were involved. Conclusions: Gamma interferon could accentuate the migration of non-specific immune cells to necrotic areas which occur spontaneously in large tumors. These results in animals bearing large tumor suggest that it may be worthwhile to explore local gamma interferon delivery to patients with extensive hepatocarcinoma.
AB - Background/Aims: Short-term efficacy of local gamma interferon delivered via a single injection of an adenovirus-gamma interferon vector has been reported in immunocompetent animals which develop spontaneous liver cancer. However the long-term outcome was not examined. The aim of this randomized trial was to assess in an immunodeficient mouse ectopic model the benefit, if any, of the long-term efficacy of intratumoral injections of gamma interferon itself. Methodology: 77 mice were randomly assigned to 4 groups. Gamma interferon treated groups received a dose of 5000, 10000 or 20000 IU per animal versus phosphate-buffered saline. The follow-up lasted 46 days. Results: Significant differences were noted in mice receiving 20000 IU compared to controls: increase in survival (p=0.0485), slowing down of tumor growth in large tumors (p=0.009), increase in necrosis (p=0.004). The preferential staining in necrotic areas with anti-Class II antibody and the accumulation of nuclear debris indicated that neutrophils were involved. Conclusions: Gamma interferon could accentuate the migration of non-specific immune cells to necrotic areas which occur spontaneously in large tumors. These results in animals bearing large tumor suggest that it may be worthwhile to explore local gamma interferon delivery to patients with extensive hepatocarcinoma.
KW - Ectopic model
KW - Hepatocarcinoma
KW - Interferon
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=3042558268&partnerID=8YFLogxK
M3 - Article
C2 - 15239257
AN - SCOPUS:3042558268
SN - 0172-6390
VL - 51
SP - 1115
EP - 1120
JO - Hepato-Gastroenterology
JF - Hepato-Gastroenterology
IS - 58
ER -