VM-26, a new anticancer drug with effectiveness in malignant lymphoma: an Eastern Cooperative Oncology Group Study (EST 1474)

Cancer Treat Rep. 1979 Jan;63(1):7-11.

Abstract

Thirty-six patients with stage III and IV Hodgkin's disease and non-Hodgkin's lymphoma, who had become refractory to conventional chemotherapy, were treated with VM-26. Complete remissions were documented in two patients with diffuse histiocytic lymphoma. Six patients (four with non-Hodgkin's lymphomas and two with Hodgkin's disease) had partial remissions. The overall response rate was 22% (eight of 36 patients). Hematologic toxicity was the most frequent dose-limiting toxicity. Nonhematologic toxic effects were mild and acceptable. This study demonstrates that VM-26 can produce tumor responses in refractory lymphomas. The Eastern Cooperative Oncology Group is currently planning two new phase II studies to incorporate VM-26 with other active new agents, one involving hexamethylmelamine and the other involving cis-dichlorodiammineplatinum(II).

Publication types

  • Clinical Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Blood Cell Count
  • Clinical Trials as Topic
  • Drug Evaluation
  • Female
  • Hodgkin Disease / drug therapy*
  • Humans
  • Lymphoma / drug therapy*
  • Male
  • Middle Aged
  • Podophyllotoxin / analogs & derivatives*
  • Teniposide / administration & dosage
  • Teniposide / adverse effects
  • Teniposide / therapeutic use*

Substances

  • Teniposide
  • Podophyllotoxin