Recombinant leukocyte interferon, doxorubicin, and 5FUDR in patients with hepatocellular carcinoma-A phase II trial

J Cancer Res Clin Oncol. 2003 Jan;129(1):17-20. doi: 10.1007/s00432-002-0398-2. Epub 2003 Jan 9.

Abstract

Purpose: To study the combination of 5FUDR, recombinant leukocyte interferon (IFN), and doxorubicin in patients with unresectable hepatocellular carcinoma.

Methods: IFN was administered at a dose of 6 miu/m(2) subcutaneously followed in 2 h by doxorubicin 20 mg/m(2) intravenously. After doxorubicin, 5FUDR was given as a 24-h infusion at a starting dose of 80 mg/kg. The dose of IFN was escalated to three times a week if tolerated. Both doxorubicin and 5FUDR were administered once weekly.

Results: There were 30 patients entered into the study. Among the 30 patients, there were two partial responses (7%) and one patient had stable disease. Toxicity was generally tolerable with fever, and chills, fatigue, and myelosuppression as the most common side effects.

Conclusions: This chemotherapy combination was generally well tolerated, but has limited activity in unresectable, advanced hepatocellular carcinoma.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Carcinoma, Hepatocellular / drug therapy*
  • Doxorubicin / administration & dosage
  • Drug Administration Schedule
  • Female
  • Floxuridine / administration & dosage
  • Humans
  • Infusions, Intravenous
  • Interferons / administration & dosage
  • Leukocytes
  • Liver Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Recombinant Proteins / administration & dosage
  • Treatment Failure

Substances

  • Recombinant Proteins
  • Floxuridine
  • Doxorubicin
  • Interferons