Phase III randomized, double-blind placebo-controlled trial of rhGM-CSF following allogeneic bone marrow transplantation

Bone Marrow Transplant. 1995 Jun;15(6):949-54.

Abstract

Preliminary studies in allogeneic BMT suggest that recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) is well tolerated. This is a prospective, multicenter, randomized, double-blind, placebo-controlled trial. Yeast-derived rhGM-CSF 250 micrograms/m2/day or placebo was administered by 4-hour i.v. infusion starting on the day of marrow infusion (day 0) to day 20. All patients received HLA-identical sibling marrow and cyclosporine and prednisone for GVHD prophylaxis. Fifty three patients received rhGM-CSF and 56 received placebo. Comparison of demographics revealed no differences. The time to achieve an absolute neutrophil count of > 0.5 x 10(9) cells/l was shortened in rhGM-CSF treated patients (day 13 vs. 17, P = 0.0001). The incidences of grade III-IV mucositis and infection were significantly reduced (P = 0.005, P = 0.001, respectively) and duration of hospitalization was modestly shortened by 1 day (P = 0.02) in rhGM-CSF treated patients. No differences in platelet recovery, erythrocyte recovery, incidence of veno-occlusive disease, GVHD severity, relapse or survival were observed. In conclusion, rhGM-CSF is well tolerated and reduces post-transplant morbidity in patients undergoing HLA-identical allogeneic BMT.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase III
  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Bone Marrow Transplantation* / adverse effects
  • Bone Marrow Transplantation* / mortality
  • Double-Blind Method
  • Female
  • Graft vs Host Disease / epidemiology
  • Graft vs Host Disease / etiology
  • Granulocyte-Macrophage Colony-Stimulating Factor / adverse effects
  • Granulocyte-Macrophage Colony-Stimulating Factor / therapeutic use*
  • HLA Antigens / immunology
  • Hematopoietic Cell Growth Factors / therapeutic use*
  • Hepatic Veno-Occlusive Disease / epidemiology
  • Hepatic Veno-Occlusive Disease / etiology
  • Humans
  • Infections / epidemiology
  • Leukemia / mortality
  • Leukemia / therapy
  • Leukocyte Count / drug effects
  • Lymphoma / mortality
  • Lymphoma / therapy
  • Male
  • Multiple Myeloma / mortality
  • Multiple Myeloma / therapy
  • Myelodysplastic Syndromes / mortality
  • Myelodysplastic Syndromes / therapy
  • Nuclear Family
  • Prospective Studies
  • Recombinant Proteins / adverse effects
  • Recombinant Proteins / therapeutic use
  • Tissue Donors
  • Transplantation, Homologous
  • Treatment Outcome

Substances

  • HLA Antigens
  • Hematopoietic Cell Growth Factors
  • Recombinant Proteins
  • Granulocyte-Macrophage Colony-Stimulating Factor