Teniposide in advanced breast cancer. A phase II trial in patients with no prior chemotherapy

Ann Oncol. 1992 May;3(5):377-8. doi: 10.1093/oxfordjournals.annonc.a058210.

Abstract

The objective response rates were determined using teniposide as first-line chemotherapy for patients with recurrent breast cancer. Twenty-seven evaluable patients with advanced disease received teniposide 70 mg/m2 i.v. days 1-5 every 3 weeks. A total of 211 courses were given. Responses included one complete (4%) and 9 partial responses (33%) with a median duration of response of 9 months (range 2-31 months). The main toxicity was myelosuppression. The results show that teniposide has at least modest activity in patients with advanced breast cancer treated previously with endocrine therapy.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Breast Neoplasms / drug therapy*
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Humans
  • Middle Aged
  • Teniposide / adverse effects
  • Teniposide / therapeutic use*

Substances

  • Teniposide