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[Phase II study of 5'-DFUR in gastrointestinal and breast cancer].

Abstract
Clinical effects of daily oral administration of 5'-DFUR were studied in patients with advanced or recurrent gastrointestinal cancer and breast cancer. Cases included 5 gastric cancer, 18 colorectal cancer, 27 breast cancer and 1 malignant melanoma. Out of 38 cases who completed the treatment, CR was observed in 2 and PR in 7, the response rate being 23.7%. Out of 23 cases with breast cancer who completed the treatment, CR was observed in 2 and PR in 6, the response rate being 34.8%. Safety was evaluated in 42 cases and diarrhea was found in 17.1% of cases; however, it was easily reduced by decreasing the dosage or discontinuing administration of the drug.
AuthorsT Tominaga, M Kitamura, K Hayashi, I Takahashi, G Kosaki
JournalGan to kagaku ryoho. Cancer & chemotherapy (Gan To Kagaku Ryoho) Vol. 12 Issue 11 Pg. 2172-8 (Nov 1985) ISSN: 0385-0684 [Print] Japan
PMID2933000 (Publication Type: Case Reports, English Abstract, Journal Article)
Chemical References
  • Antineoplastic Agents
  • Floxuridine
  • doxifluridine
Topics
  • Administration, Oral
  • Adult
  • Aged
  • Antineoplastic Agents (adverse effects, therapeutic use)
  • Breast Neoplasms (drug therapy)
  • Colonic Neoplasms (drug therapy)
  • Diarrhea (chemically induced)
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Floxuridine (adverse effects, therapeutic use)
  • Humans
  • Leukopenia (chemically induced)
  • Lymphatic Metastasis
  • Male
  • Melanoma (drug therapy)
  • Middle Aged
  • Nausea (chemically induced)
  • Rectal Neoplasms (drug therapy)
  • Stomach Neoplasms (drug therapy)

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