Immunosuppression without steroids in liver transplantation is safe and reduces infection and metabolic complications: results from a prospective multicenter randomized study

J Hepatol. 2006 Apr;44(4):710-6. doi: 10.1016/j.jhep.2005.12.010. Epub 2006 Jan 24.

Abstract

Background/aims: The purpose of this study was to evaluate the efficacy of a steroid-free immunosuppression protocol.

Methods: From 2001 to 2004, 198 liver-transplant patients were randomized to receive immunosuppression with Basiliximab and cyclosporine, with (St Group) or without (NoSt Group) prednisone. The primary end points were acute rejection, and patient and graft survival. The secondary end points were infection, metabolic complications, and hepatitis C-virus recurrence.

Results: Overall rejection rate was 15%, with no differences (St: 13% vs NoSt: 18%; P=0.33). Infection rate was similar in both groups (St: 51% vs NoSt: 47%; P=0.56), but diabetic patients in the St Group had a significantly higher rate of bacterial infections (St: 54% vs NoSt: 14%; P=0.005). The six-month protocol biopsies showed hepatitis C recurrence in 90% of patients, without differences between groups. Hypertension was more frequent in the St Group (St: 44% vs NoSt: 25%; P=0.006). De novo diabetes rate was higher in the St Group (month 1: St: 29% vs NoSt: 18%; P=0.06), with higher glycatedHb (5.1+/-1.1 vs 4.4+/-0.8; P=0.002). Six-month survival rates were similar (St: 89% vs NoSt: 94%, P=0.62).

Conclusions: Immunosuppression without steroids is safe and reduces infection and metabolic complications.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / therapeutic use*
  • Basiliximab
  • Cyclosporine / immunology
  • Cyclosporine / therapeutic use*
  • Diabetes Mellitus / etiology
  • Diabetes Mellitus / physiopathology
  • Drug Therapy, Combination
  • Female
  • Graft Rejection
  • Graft Survival
  • Hepacivirus / immunology
  • Hepatitis C / drug therapy*
  • Hepatitis C / etiology*
  • Hepatitis C / mortality
  • Hepatitis C / surgery
  • Humans
  • Hypertension / etiology
  • Hypertension / physiopathology
  • Immunosuppression Therapy / methods*
  • Immunosuppressive Agents / adverse effects
  • Immunosuppressive Agents / immunology
  • Immunosuppressive Agents / therapeutic use*
  • Liver / chemistry
  • Liver / pathology
  • Liver / virology
  • Liver Transplantation / adverse effects*
  • Liver Transplantation / immunology
  • Liver Transplantation / mortality
  • Male
  • Middle Aged
  • Prednisone / immunology
  • Prednisone / therapeutic use*
  • Prospective Studies
  • Recombinant Fusion Proteins / immunology
  • Recombinant Fusion Proteins / therapeutic use*
  • Recurrence
  • Steroids / immunology
  • Steroids / therapeutic use
  • Survival Rate
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Immunosuppressive Agents
  • Recombinant Fusion Proteins
  • Steroids
  • Cyclosporine
  • Basiliximab
  • Prednisone