First-line treatment of Waldenström's disease with cladribine. Arbeitsgemeinschaft Medikamentöse Tumortherapie

Ann Hematol. 1997 Jan;74(1):7-10. doi: 10.1007/s002770050247.

Abstract

Purpose: To assess the activity and side effects of cladribine (2-CdA) treatment in patients with advanced Waldenström's disease.

Patients and methods: Ten symptomatic patients without prior therapy were included in a prospective multicenter trial. 2-CdA was administered daily at 0.12 mg/kg body weight in a 2-h i.v. infusion over 5 consecutive days: this was repeated every 28 days for four cycles. Patients achieving a remission received interferon alfa-2c (1F) 15 micrograms s.c. three times a week for 1 year.

Results: All 10 patients responded to 2-CdA (100%; 95% confidence interval, 68-100%), with one complete (CR) and eight partial responders (PR): one patient had only one 2-CdA cycle and showed a minor improvement (MR). Patients tolerated the treatment well. Despite considerable immunosuppression, an infection occurred in only two patients. After a median observation period of 57 weeks, three patients had shown progression, including one who died of lymphoma.

Conclusion: 2-CdA induction and IF maintenance is a well-tolerated therapy for symptomatic untreated patients with advanced Waldenström's disease and offers excellent palliation.

Publication types

  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / therapeutic use*
  • Cladribine / adverse effects
  • Cladribine / therapeutic use*
  • Female
  • Humans
  • Interferon Type I / therapeutic use
  • Male
  • Middle Aged
  • Neutropenia / chemically induced
  • Prospective Studies
  • Recombinant Proteins
  • Remission Induction
  • Waldenstrom Macroglobulinemia / drug therapy*

Substances

  • Antineoplastic Agents
  • Interferon Type I
  • Recombinant Proteins
  • Cladribine