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Phase II trial of merbarone in soft tissue sarcoma. A Southwest Oncology Group study.

Abstract
Thirty-seven patients with advanced soft tissue sarcoma were treated with merbarone utilizing a daily intravenous schedule for five days. Only one partial response was observed in the thirty-three evaluable patients. The major toxicities were renal, with elevation of creatinine and/or proteinuria, and gastrointestinal, with mild to moderate nausea and vomiting. Merbarone in this dose and schedule has minimal activity in soft tissue sarcoma.
AuthorsE H Kraut, J Bendetti, S P Balcerzak, J H Doroshow
JournalInvestigational new drugs (Invest New Drugs) Vol. 10 Issue 4 Pg. 347-9 (Nov 1992) ISSN: 0167-6997 [Print] United States
PMID1487411 (Publication Type: Clinical Trial, Clinical Trial, Phase II, Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antineoplastic Agents
  • Thiobarbiturates
  • merbarone
Topics
  • Adult
  • Aged
  • Antineoplastic Agents (administration & dosage, adverse effects, therapeutic use)
  • Drug Administration Schedule
  • Female
  • Humans
  • Infusions, Intravenous
  • Male
  • Middle Aged
  • Sarcoma (drug therapy)
  • Soft Tissue Neoplasms (drug therapy)
  • Thiobarbiturates (administration & dosage, adverse effects, therapeutic use)

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