Impact of cyclosporine levels on the development of acute graft versus host disease after reduced intensity conditioning allogeneic stem cell transplantation

Mediators Inflamm. 2014:2014:620682. doi: 10.1155/2014/620682. Epub 2014 Jan 30.

Abstract

We analyze the impact of cyclosporine (CsA) levels in the development of acute graft-versus-host disease (aGVHD) after reduced intensity conditioning allogeneic hematopoietic transplantation (allo-RIC). We retrospectively evaluated 156 consecutive patients who underwent HLA-identical sibling allo-RIC at our institution. CsA median blood levels in the 1st, 2nd, 3rd and 4th weeks after allo-RIC were 134 (range: 10-444), 219 (54-656), 253 (53-910) and 224 (30-699) ng/mL; 60%, 16%, 11% and 17% of the patients had median CsA blood levels below 150 ng/mL during these weeks. 53 patients developed grade 2-4 aGVHD for a cumulative incidence of 45% (95% CI 34-50%) at a median of 42 days. Low CsA levels on the 3rd week and sex-mismatch were associated with the development of GVHD. Risk factors for 1-year NRM and OS were advanced disease status (HR: 2.2, P = 0.02) and development of grade 2-4 aGVHD (HR: 2.5, P < 0.01), while there was a trend for higher NRM in patients with a low median CsA concentration on the 3rd week (P = 0.06). These results emphasize the relevance of sustaining adequate levels of blood CsA by close monitoring and dose adjustments, particularly when engraftment becomes evident. CsA adequate management will impact on long-term outcomes in the allo-RIC setting.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Alleles
  • Cyclosporine / administration & dosage*
  • Female
  • Graft vs Host Disease / drug therapy*
  • HLA Antigens / chemistry
  • Humans
  • Immunosuppressive Agents / administration & dosage
  • Immunosuppressive Agents / therapeutic use
  • Male
  • Middle Aged
  • Retrospective Studies
  • Risk Factors
  • Stem Cell Transplantation / adverse effects*
  • Stem Cell Transplantation / methods
  • Time Factors
  • Transplantation Conditioning / methods*
  • Transplantation, Homologous / adverse effects*
  • Transplantation, Homologous / methods
  • Young Adult

Substances

  • HLA Antigens
  • Immunosuppressive Agents
  • Cyclosporine