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Phase II study of 3-deazauridine in advanced colorectal adenocarcinoma.

Abstract
A phase II study of 3-deazauridine (DAUR) showed poor activity in previously treated patients with advanced colorectal adenocarcinoma. There were no responses among 15 patients treated on a dose schedule of 1200 mg/m2/day for 5 days repeated at 3-week intervals. Toxicity included mild nausea and vomiting, occasional mucositis, diarrhea, and dizziness. A minimal degree of myelosuppression was observed.
AuthorsS Bruno, P J Creaven, E Ledesma, D Poster, J Yoon, A Mittelman
JournalAmerican journal of clinical oncology (Am J Clin Oncol) Vol. 5 Issue 1 Pg. 69-71 (Feb 1982) ISSN: 0277-3732 [Print] United States
PMID7081140 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antineoplastic Agents
  • 3-Deazauridine
  • Uridine
Topics
  • 3-Deazauridine (administration & dosage, adverse effects)
  • Adenocarcinoma (drug therapy)
  • Adult
  • Aged
  • Antineoplastic Agents (administration & dosage, adverse effects)
  • Colonic Neoplasms (drug therapy)
  • Digestive System (drug effects)
  • Drug Evaluation
  • Female
  • Humans
  • Male
  • Middle Aged
  • Rectal Neoplasms (drug therapy)
  • Uridine (analogs & derivatives)

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