Phase II study of cytarabine in Hodgkin's disease. The EORTC Lymphoma Cooperative Group

Eur J Cancer. 1992;28A(4-5):857-9. doi: 10.1016/0959-8049(92)90133-m.

Abstract

Cytarabine was administered to 24 patients with previously treated Hodgkin's disease in the EORTC Lymphoma Cooperative Group. The drug was administered at the dose of 80 mg/m2 subcutaneously twice a day on 5 consecutive days every 3 weeks. The overall response rate was 17.6% (3 responses among 17 evaluable patients) with a short duration (2-6 months). The main toxicity was myelosuppression. Our experience in the EORTC Lymphoma Cooperative Group could not demonstrate a significant activity at this dose and schedule in Hodgkin's disease.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Cytarabine / adverse effects
  • Cytarabine / therapeutic use*
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Hodgkin Disease / drug therapy*
  • Humans
  • Male
  • Middle Aged

Substances

  • Cytarabine