Cytotoxic agents active against mucinous adenocarcinoma of the ovary

Oncol Rep. 1998 Jan-Feb;5(1):99-101. doi: 10.3892/or.5.1.99.

Abstract

The purpose of the present study was to evaluate cytotoxic agents active for mucinous adenocarcinoma of the ovary (MACO) which is considered to be intrinsically platinum-resistant. We first conducted in vitro chemosensitivity tests assessing cytotoxic activities of various anti-cancer agents against MACO using a cell line, designated OMC-3, established from ascites of a patient with histologically pure MACO. The most active single agent was SN-38 (active substance of CPT-11 in vivo). The second most potent agent was mitomycin-C (MMC) followed by doxorubicin (DOX). In vivo chemo-sensitivity test of agents on OMC-3 transplanted into Balb/c nude mice demonstrated that MMC was most potent, followed by DOX. Moreover, a combination of CPT-11 and MMC exhibited the highest anti-tumor activity in this animal model. Cisplatin was found to be ineffective in both the in vitro and in vivo experimental system. Clinical trial with a combination of MMC and CPT-11 are justified in patients with MACO.

MeSH terms

  • Adenocarcinoma, Mucinous / drug therapy*
  • Adenocarcinoma, Mucinous / pathology
  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Agents / toxicity
  • Antineoplastic Agents, Phytogenic / therapeutic use
  • Antineoplastic Agents, Phytogenic / toxicity
  • Camptothecin / analogs & derivatives
  • Camptothecin / therapeutic use
  • Camptothecin / toxicity
  • Cell Division / drug effects
  • Cisplatin / therapeutic use*
  • Cisplatin / toxicity
  • Doxorubicin / therapeutic use
  • Doxorubicin / toxicity
  • Drug Resistance, Neoplasm
  • Etoposide / therapeutic use
  • Etoposide / toxicity
  • Female
  • Humans
  • Irinotecan
  • Mice
  • Mice, Nude
  • Mitomycin / therapeutic use
  • Mitomycin / toxicity
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / pathology
  • Transplantation, Heterologous
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Antineoplastic Agents, Phytogenic
  • Mitomycin
  • Etoposide
  • Irinotecan
  • Doxorubicin
  • Cisplatin
  • Camptothecin