A phase I clinical trial of didemnin B.

Abstract

Didemnin B is a depsipeptide extracted from the marine tunicate Trididemnin cyanophorum. This agent is a potent inhibitor of L1210 growth in vitro and has activity against murine B16 melanoma, P388 leukemia, and M5076 sarcoma in vivo. The results of preclinical toxicologic tests demonstrated abnormalities in clotting parameters thought to be secondary to drug-induced liver dysfunction. Thirty-five patients with advanced cancer received didemnin B according to a 5-day bolus schedule with dose levels ranging from 0.03 to 2.00 mg/m2/d. The dose-limiting toxicity was nausea and vomiting. Sporadic elevation of the hepatic enzyme level occurred but was not dose limiting. Two patients had anaphylactic symptoms possibly related to the 5% polyoxyethylated castor oil (Cremophor EL, BASF, Ludwigshafen, Germany) vehicle during the drug infusion. Clinical bleeding was not observed and myelosuppression was not significant. No partial or complete tumor responses were seen. The recommended Phase II dose for the 5-day schedule is 1.6 mg/m2/d.

• Authors: J A Stewart, J B Low, J D Roberts, A Blow
• Journal: Cancer (Cancer) Vol. 68 Issue 12 Pg. 2550-4 (Dec 15 1991) ISSN: 0008-543X [Print] United States
• PMID: 1933801 (Publication Type: Clinical Trial, Journal Article, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Antineoplastic Agents
• Depsipeptides
• Peptides, Cyclic
• didemnins

Topics

• Adult
• Aged
• Antineoplastic Agents (adverse effects, therapeutic use)
• Depsipeptides
• Drug Evaluation
• Female
• Humans
• Male
• Middle Aged
• Molecular Structure
• Neoplasms (drug therapy)
• Peptides, Cyclic (adverse effects, therapeutic use)