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Phase I evaluation of beta-2'-deoxythioguanosine in pediatric patients with leukemia.

Abstract
Thirty-one pediatric patients with acute leukemia who had relapsed on either 6-mercaptopurine or 6-thioguanine were treated with beta-2'-deoxythioguanosine, which was administered as an iv infusion every 12 hours for three or six doses every 2 weeks. Severe nausea and vomiting and urate nephropathy were the dose-limiting toxic effects. Therapeutic responses occurred in four of 24 children with acute lymphocytic leukemia and in two of seven with acute nonlymphoblastic leukemia.
AuthorsG R Higgins, D C Jamin, N A Shore, R Momparler, G Hartman, S E Siegel
JournalCancer treatment reports (Cancer Treat Rep) Vol. 69 Issue 6 Pg. 699-701 (Jun 1985) ISSN: 0361-5960 [Print] United States
PMID3860294 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Thionucleosides
  • Uric Acid
  • beta-2'-deoxythioguanosine
  • Deoxyguanosine
Topics
  • Acute Disease
  • Acute Kidney Injury (chemically induced)
  • Child
  • Deoxyguanosine (analogs & derivatives, therapeutic use, toxicity)
  • Drug Evaluation
  • Humans
  • Leukemia (drug therapy)
  • Leukemia, Lymphoid (drug therapy)
  • Nausea (chemically induced)
  • Thionucleosides (therapeutic use, toxicity)
  • Uric Acid (urine)
  • Vomiting (chemically induced)

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