Efficacy and feasibility of IDEA therapy for refractory or relapsed non-Hodgkin's lymphoma

Anticancer Res. 2009 May;29(5):1749-54.

Abstract

Background: The effects of a novel salvage regimen, IDEA (ifosfamide, cytosine arabinoside, etoposide and dexamethasone), which does not include anthracycline or platinum, in patients with non-Hodgkin's lymphoma (NHL) were examined.

Patients and methods: Thirty-four patients with refractory or relapsed NHL were treated with IDEA.

Results: The overall remission and complete remission rates were 67.6% and 35.3%, respectively. The toxicity of IDEA was tolerable. With a median follow-up of 14 months, one-year overall survival (OS) and progression-free survival rates were 75.1% and 43.7%, respectively. Adequate numbers of CD34(+) cells were obtained in 77.8% of the patients assigned to receive autologous peripheral blood stem cell (PBSC) transplantation. High-dose chemotherapy with autologous PBSC transplantation was carried out in 14 patients; their 3-year OS was 75.0%, with a median follow-up of 38 months.

Conclusion: IDEA is an effective second-line chemotherapy regimen for NHL patients and has an excellent PBSC-mobilizing effect.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Cytarabine / adverse effects
  • Cytarabine / therapeutic use
  • Dexamethasone / adverse effects
  • Dexamethasone / therapeutic use
  • Etoposide / adverse effects
  • Etoposide / therapeutic use
  • Feasibility Studies
  • Female
  • Humans
  • Ifosfamide / adverse effects
  • Ifosfamide / therapeutic use
  • Lymphoma, Non-Hodgkin / drug therapy*
  • Male
  • Middle Aged
  • Recurrence
  • Retrospective Studies
  • Salvage Therapy

Substances

  • Cytarabine
  • Etoposide
  • Dexamethasone
  • Ifosfamide

Supplementary concepts

  • G-IDEA protocol