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Suppressive effect of bevacizumab on peritoneal dissemination from gastric cancer in a peritoneal metastasis model

Purpose Vascular endothelial growth factor (VEGF) has been reported to enhance vascular permeability and angiogenesis in the abdominal wall, thereby contributing to peritoneal dissemination with malignant ascites. We conducted this experimental study to find out if bevacizumab, a humanized monoclona...

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Published in:Surgery today (Tokyo, Japan) Japan), 2010-09, Vol.40 (9), p.851-857
Main Authors: Imaizumi, Takuya, Aoyagi, Keishiro, Miyagi, Motoshi, Shirouzu, Kazuo
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container_title Surgery today (Tokyo, Japan)
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creator Imaizumi, Takuya
Aoyagi, Keishiro
Miyagi, Motoshi
Shirouzu, Kazuo
description Purpose Vascular endothelial growth factor (VEGF) has been reported to enhance vascular permeability and angiogenesis in the abdominal wall, thereby contributing to peritoneal dissemination with malignant ascites. We conducted this experimental study to find out if bevacizumab, a humanized monoclonal antibody against VEGF, had a suppressive effect on peritoneal dissemination from gastric cancer, in an experimental nude mouse model of peritoneal metastasis. Methods Each mouse was treated with a single intraperitoneal (i.p.) injection of bevacizumab. Five mice were killed, and we measured their body weight, the mean number of tumor nodules, and the volume of ascites. We also extracted retroperitoneal tissues for histological examination, to count the frequency of mitosis, and to calculate the mitotic index. Another five mice were monitored until death, and their mean survival duration was calculated. Results The volume of ascites and the mitotic index were significantly lower in the therapy group than in the nontherapy group ( P = 0.042 and P < 0.01, respectively). The survival curve of the therapy group was significantly higher than that of the nontherapy group ( P = 0.005). Conclusion Bevacizumab may suppress peritoneal dissemination from gastric cancer.
doi_str_mv 10.1007/s00595-009-4154-y
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We conducted this experimental study to find out if bevacizumab, a humanized monoclonal antibody against VEGF, had a suppressive effect on peritoneal dissemination from gastric cancer, in an experimental nude mouse model of peritoneal metastasis. Methods Each mouse was treated with a single intraperitoneal (i.p.) injection of bevacizumab. Five mice were killed, and we measured their body weight, the mean number of tumor nodules, and the volume of ascites. We also extracted retroperitoneal tissues for histological examination, to count the frequency of mitosis, and to calculate the mitotic index. Another five mice were monitored until death, and their mean survival duration was calculated. Results The volume of ascites and the mitotic index were significantly lower in the therapy group than in the nontherapy group ( P = 0.042 and P &lt; 0.01, respectively). The survival curve of the therapy group was significantly higher than that of the nontherapy group ( P = 0.005). 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subjects Angiogenesis Inhibitors - administration & dosage
Animals
Antibodies, Monoclonal - administration & dosage
Antibodies, Monoclonal, Humanized
Ascites - pathology
Bevacizumab
Cell Line, Tumor
Injections, Intraperitoneal
Male
Medicine
Medicine & Public Health
Mice
Mice, Inbred BALB C
Mice, Nude
Mitotic Index
Neoplasm Transplantation
Original Article
Peritoneal Neoplasms - pathology
Peritoneal Neoplasms - prevention & control
Peritoneal Neoplasms - secondary
Stomach Neoplasms - pathology
Surgery
Surgical Oncology
Vascular Endothelial Growth Factor A - immunology
title Suppressive effect of bevacizumab on peritoneal dissemination from gastric cancer in a peritoneal metastasis model
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