High dose epirubicin in refractory or relapsed non-seminomatous testicular cancer: a phase II study

Ann Oncol. 1990 Sep;1(5):375-6. doi: 10.1093/oxfordjournals.annonc.a057778.

Abstract

Sixteen patients with metastatic nonseminomatous testicular cancer refractory to cisplatinum combination chemotherapy, were treated with epirubicin 100-120 mg/m2 q d 22. One partial remission lasting 6 months was achieved. Two additional patients had stabilisation of disease for 3 and 4 months. Median time to progression was 43 days. Myelosuppression was dose-limiting, with a WBC nadir of 1900/microliters. 4/30 cycles (13%) were associated with granulocytopenic fever. One patient developed a decline in cardiac ejection fraction without clinical signs of congestive heart failure. Epirubicin in this dosage and schedule has no major therapeutic activity in heavily pretreated non-seminomatous testicular cancer.

Publication types

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

MeSH terms

  • Combined Modality Therapy
  • Drug Administration Schedule
  • Drug Evaluation
  • Epirubicin / administration & dosage*
  • Humans
  • Male
  • Neoplasm Recurrence, Local / drug therapy*
  • Remission Induction
  • Survival Rate
  • Testicular Neoplasms / drug therapy*
  • Testicular Neoplasms / mortality

Substances

  • Epirubicin