Camptothecin analogues/cisplatin: an effective treatment of advanced bladder cancer in a preclinical in vivo model system

J Urol. 1998 Jul;160(1):252-6. doi: 10.1016/s0022-5347(01)63099-4.

Abstract

Objective: To evaluate the impact of the camptothecin analogs on human TCC xenograft, both as monotherapy and in combination with cisplatin (CDDP).

Materials and methods: Human transitional cell carcinoma (TCC) xenograft tumor line (DU4184) tested by subrenal capsule assay in 112 nude mice(NM-SRCA). CDDP and the camptothecin analogs irinotecan (CPT-11) and 9-aminocamptothecin(9-AC) were evaluated.

Results: Both of the camptothecin analogs showed significant short term tumor inhibition which translated into enhanced survival. Maximal tumor inhibition (>95%) was achieved when either of the camptothecin analogs was combined with CDDP with minimal host toxicity. This translated into 400% increase in median survival. While all controls were dead 39 days following tumor implantation, none of the combination treated animals had died.

Conclusion: The combination of CDDP with these camptothecin analogs is an effective therapy against this model of advanced TCC. These observations suggest potential clinical value.

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Camptothecin / analogs & derivatives*
  • Camptothecin / therapeutic use
  • Cisplatin / therapeutic use*
  • Drug Screening Assays, Antitumor
  • Humans
  • Irinotecan
  • Mice
  • Mice, Inbred BALB C
  • Neoplasm Staging
  • Tumor Cells, Cultured / transplantation
  • Urinary Bladder Neoplasms / drug therapy*
  • Urinary Bladder Neoplasms / pathology

Substances

  • Antineoplastic Agents
  • 9-aminocamptothecin
  • Irinotecan
  • Cisplatin
  • Camptothecin