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[Phase II study of FF-705 by Clinical Cooperative Study Group].

Abstract
Clinical efficacy of new fluorouridine derivative, FF-705, was studied in 108 patients with advanced malignant tumors. Partial responses were observed in 8 of 61 evaluable cases (13.1%): 4 of 9 patients with breast cancer, 1 of 19 patients with gastric cancer, 1 of 15 patients with lung cancer, 1 of 3 patients with kidney cancer and 1 of 1 patient with pancreas cancer. In the analysis of adverse effects of FF-705, gastrointestinal toxicity was major toxicity. Especially, diarrhea was observed in 41 of 108 patients (38.0%) within a total dose of 10 g shortly after drug administration.
Authors
JournalGan to kagaku ryoho. Cancer & chemotherapy (Gan To Kagaku Ryoho) Vol. 11 Issue 1 Pg. 150-6 (Jan 1984) ISSN: 0385-0684 [Print] Japan
PMID6230055 (Publication Type: English Abstract, Journal Article)
Chemical References
  • Capsules
  • Floxuridine
  • 2'-deoxy-3',5'-di-O-acetyl-5-fluoro-3-(3-methylbenzoyl)uridine
Topics
  • Administration, Oral
  • Adult
  • Aged
  • Breast Neoplasms (drug therapy)
  • Capsules
  • Colonic Neoplasms (drug therapy)
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Floxuridine (analogs & derivatives, therapeutic use)
  • Humans
  • Lung Neoplasms (drug therapy)
  • Male
  • Middle Aged
  • Neoplasms (drug therapy)
  • Stomach Neoplasms (drug therapy)

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