Chemo-immunotherapy of ovarian cancer in a murine tumour model

Citation
Ah. Klimp et al., Chemo-immunotherapy of ovarian cancer in a murine tumour model, ANTICANC R, 20(4), 2000, pp. 2585-2592
Citations number
32
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
4
Year of publication
2000
Pages
2585 - 2592
Database
ISI
SICI code
0250-7005(200007/08)20:4<2585:COOCIA>2.0.ZU;2-9
Abstract
Background: As a majority of ovarian cancer patients will ultimately develo p recurrent disease, there is an urgent need for alternative or additional approaches in the treatment of this cancer. Materials and Methods: The anti tumour effect of i.p. administered cisplatin, liposomal muramyltripeptide p hosphatidylethanolamine (L-MTP-PE) and granulocyte-macrophage colony-stimul ating factor (GM-CSF) were investigated using an ip. growing murine ovarian tumour. Tumour growth was followed by measuring weight and survival of the mice. Results: An i.p. injection of L-MTP-PE in non-tumour bearing mice re sulted in an approximately 10-fold increase in the number of peritoneal cel ls, which were highly cytotoxic. Nonetheless, treatment of mice inoculated with MOT cells with cisplatin, L-MTP-PE and GM-CSF using different treatmen t schedules did not result in inhibited tumour growth when compared to trea tment with cisplatin alone. Conclusion: Although L-MTP-PE showed art enormo us increase in peritoneal cells with high tumour cytotoxic capacity, the im munotherapeutic treatment with GM-CSF and L-MTP-PE, aimed at the recruitmen t and activation of the peritoneal cell population, failed to result in a s ignificant prolongation of survival.