PubMed · 3690532
Phase I study of echinomycin.
Abstract
Echinomycin was administered to patients with advanced carcinoma in escalating doses ranging from 60 to 1500 micrograms/m2 given weekly by 15-minute iv infusions for four doses, with a subsequent 2-week rest period. Dose-limiting nausea, vomiting, and anorexia associated with varying degrees of renal and hepatic dysfunction proved dose-limiting at the 1500-micrograms/m2 level. Thrombocytopenia was noted in 15% of patients receiving greater than or equal to 700 micrograms/m2 and was severe in 11% without an evident dose-response relationship. Leukopenia was rare and mild when encountered. Allergic reactions were observed. Phase II trials are feasible using a dose schedule of 1200 micrograms/m2/week X 4 weeks.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
R Pazdur, C D Haas, L H Baker, C G Leichman, D Decker. 1987. Phase I study of echinomycin.. https://pubmed.ncbi.nlm.nih.gov/3690532/
Cite the original work for its findings. Save a collection to share your selection of sources.