Phase II study of teniposide in patients with AIDS-related Kaposi's sarcoma

Eur J Cancer. 1991;27(12):1637-9. doi: 10.1016/0277-5379(91)90434-f.

Abstract

Antitumour activity of cytotoxic agents, evaluated in patients with AIDS-related Kaposi's sarcoma (KS), is about 30-80%. However, responses are mostly partial and short. Experience with etoposide is similar. Teniposide has a longer elimination half-life and superior antitumour activity compared with etoposide in some experimental models. Thus a phase II trial was done in 25 patients with AIDS-related KS. Teniposide was given by 60-min infusion at 360 mg/m2 every 3 weeks. 10 (40%) showed a partial response, median duration of 9 (6-20) weeks. The main side-effects were leukopenia, thrombocytopenia, nausea and vomiting, alopecia and mucositis.

MeSH terms

  • Acquired Immunodeficiency Syndrome / complications*
  • Adult
  • Alopecia / chemically induced
  • Drug Evaluation
  • Humans
  • Leukopenia / chemically induced
  • Male
  • Nausea / chemically induced
  • Sarcoma, Kaposi / drug therapy*
  • Sarcoma, Kaposi / etiology
  • Teniposide / adverse effects
  • Teniposide / therapeutic use*
  • Thrombocytopenia / chemically induced
  • Time Factors

Substances

  • Teniposide