[DNA topoisomerase inhibitor]

Gan To Kagaku Ryoho. 1992 Nov;19(13):2140-5.
[Article in Japanese]

Abstract

CPT-11 and Topotecan are a new semisynthetic derivative of CPT, and have been shown to inhibit DNA topoisomerase I and to have a strong antitumor activity with low toxicity against murine tumor. On the other hard, the new antitumor compounds, NC-190 and IST-622 have been shown to inhibit DNA topoisomerase II, and the clinical study are currently under progress. A phase II study of CPT-11 demonstrated that CPT-11 was a very active agent which a acceptable toxicities against patient with advanced non-small cell lung cancer and small cell lung cancer.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / therapeutic use*
  • Camptothecin / administration & dosage
  • Camptothecin / analogs & derivatives*
  • Camptothecin / therapeutic use
  • Carcinoma, Non-Small-Cell Lung / drug therapy
  • Carcinoma, Small Cell / drug therapy
  • Drug Administration Schedule
  • Female
  • Humans
  • Irinotecan
  • Lung Neoplasms / drug therapy*
  • Male
  • Mice
  • Phenazines / therapeutic use
  • Topoisomerase I Inhibitors*
  • Topotecan

Substances

  • Antineoplastic Agents
  • Phenazines
  • Topoisomerase I Inhibitors
  • NC 190
  • Irinotecan
  • Topotecan
  • Camptothecin