Phase II study of high-dose ifosfamide in hepatocellular carcinoma

Cancer Chemother Pharmacol. 1993;31(4):338-9. doi: 10.1007/BF00685682.

Abstract

A phase II study of high-dose ifosfamide in hepatocellular carcinoma was conducted among 17 Chinese patients. The dose of ifosfamide used was 2.5 g/m2 daily given as a continuous infusion for 5 days. In all, 15 patients were evaluable for tumour response. There was no complete or partial responder. The treatment was well tolerated. The most frequent toxicity was alopecia, which occurred in 11 patients, and 5 patients developed mild haematological toxicity. There was no evidence of liver or bladder toxicity. Overall, 14 patients were evaluable for survival. The median survival was 92 days (range, 30-568 days). We conclude that high-dose ifosfamide is well tolerated but ineffective in hepatocellular carcinoma in Chinese patients.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Alopecia / chemically induced
  • Carcinoma, Hepatocellular / drug therapy*
  • Clinical Trials, Phase II as Topic
  • Female
  • Humans
  • Ifosfamide / adverse effects
  • Ifosfamide / therapeutic use*
  • Liver Neoplasms / drug therapy*
  • Male
  • Middle Aged

Substances

  • Ifosfamide