Teniposide (VM-26) in patients with advanced refractory ovarian cancer: a phase II study of the Netherlands Joint Study Group for Ovarian Cancer

Eur J Cancer Clin Oncol. 1987 Jul;23(7):997-8. doi: 10.1016/0277-5379(87)90348-8.

Abstract

In 23 evaluable patients with advanced ovarian epithelial cancer refractory to combination therapy with cisplatin and an alkylating agent, teniposide (VM-26) was administered as a short-term i.v. infusion at a dose of 100 mg/m2 on days 1 and 2, every 3 weeks. Toxicity was moderate and comparable to the pattern known from other studies. No objective response has been observed, showing that teniposide is not active as second-line therapy in this disease.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Drug Evaluation
  • Female
  • Hematologic Diseases / chemically induced
  • Humans
  • Nausea / chemically induced
  • Ovarian Neoplasms / drug therapy*
  • Podophyllotoxin / analogs & derivatives*
  • Prognosis
  • Teniposide / adverse effects
  • Teniposide / therapeutic use*

Substances

  • Teniposide
  • Podophyllotoxin