GM-CSF instead of autologous bone-marrow transplantation after the BEAM regimen

Lancet. 1991 Sep 7;338(8767):601-2. doi: 10.1016/0140-6736(91)90609-s.

Abstract

Five patients with resistant non-Hodgkin lymphoma (NHL) were given granulocyte-macrophage colony-stimulating factor (GM-CSF, 250 micrograms/m2 daily) after the BEAM pretransplant chemotherapy regimen (carmustine 300 mg/m2, etoposide 1.2 g/m2, cytarabine 800 mg/m2, melphalan 140 mg/m2) because persistent lymphoma cell infiltration of the bone marrow precluded autologous bone-marrow transplantation (BMT). In three patients full haemopoietic reconstitution occurred, with similar kinetics to that seen after autologous BMT. The other two patients died without sustained haemopoietic recovery. GM-CSF may replace autologous BMT in highly selected cases of NHL with progressive disease and bone-marrow involvement.

Publication types

  • Clinical Trial

MeSH terms

  • Adolescent
  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Bone Marrow Transplantation
  • Carmustine / therapeutic use
  • Cytarabine / therapeutic use
  • Drug Evaluation
  • Etoposide / therapeutic use
  • Female
  • Granulocyte-Macrophage Colony-Stimulating Factor / therapeutic use*
  • Hematopoiesis / drug effects
  • Hematopoietic System / drug effects
  • Humans
  • Lymphoma, Non-Hodgkin / drug therapy*
  • Male
  • Melphalan / therapeutic use
  • Middle Aged
  • Transplantation, Autologous

Substances

  • Cytarabine
  • Etoposide
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Melphalan
  • Carmustine

Supplementary concepts

  • BEAM regimen