Phase II trial of 5-fluorouracil and recombinant interferon alfa-2B in metastatic colorectal carcinoma

Eur J Cancer. 1992;28A(11):1820-3. doi: 10.1016/0959-8049(92)90012-q.

Abstract

Between February 1990 and April 1991, 59 previously untreated patients with progressive and/or symptomatic metastatic colorectal carcinoma were enrolled in a phase II study of 5-fluorouracil (5-FU) and interferon alfa-2b (IFN-alpha). 5-FU 750 mg/m2/day was administered as continuous infusion for 5 days, then weekly in a dose of 750 mg/m2 as intravenous push injection starting on day 15. IFN-alpha 9 MU was given subcutaneously three times a week. Treatment was given for a maximum of 6 months. 55 patients are evaluable for response and 51 for toxicity. 17 patients (31%) achieved a partial remission, 15 (27%) had stable disease and 21 patients (38%) had progressive disease. Median duration of remission was 5 months and median survival for all patients 10 months. Toxicity was important with two treatment-related deaths and severe leukopenia, fever, diarrhoea and mucositis in about one third of the patients. In our opinion, this regimen is effective but rather toxic in metastatic colorectal carcinoma.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Colorectal Neoplasms / drug therapy*
  • Diarrhea / chemically induced
  • Drug Evaluation
  • Female
  • Fluorouracil / administration & dosage
  • Humans
  • Interferon Type I / administration & dosage
  • Leukopenia / chemically induced
  • Male
  • Middle Aged
  • Recombinant Proteins
  • Stomatitis / chemically induced

Substances

  • Interferon Type I
  • Recombinant Proteins
  • Fluorouracil