首页 | 本学科首页   官方微博 | 高级检索  
检索        


Early steroid withdrawal after liver transplantation: The canadian tacrolimus versus microemulsion cyclosporin a trial: 1-year follow-up
Institution:1. Département des Sciences de l''activité physique, Université du Québec à Montréal (UQÀM), Montréal, Québec, Canada;2. Groupe de recherche en activité physique adaptée, Université du Québec à Montréal (UQÀM), Montréal, Québec, Canada;3. Centre de recherche de l''institut universitaire de gériatrie de Montréal, Montréal, Québec, Canada;4. Department of Biomedical Sciences, University of Padova, Padova, Italy;5. Centre Hospitalier Universitaire de Lyon Sud, Lyon, France;6. Université Claude Bernard Lyon1, Faculté Lyon Sud, Inserm U 1060, France;1. Aix Marseille Univ, CNRS, LPC, Marseille, France;2. Institut Jean Nicod, Département d’études cognitives, ENS, EHESS, PSL Research University, CNRS, Paris France;3. Centre for Language Evolution, School of Philosophy, Psychology, and Language Sciences, University of Edinburgh, Edinburgh EH8 9AD, United Kingdom;4. Departments of Cognitive Science and of Philosophy, Central European University, Budapest, Hungary;5. Institut Jean Nicod (CNRS, EHESS, ENS), Paris, France
Abstract:Corticosteroid therapy contributes significant toxicity to liver transplantation. The safety and efficacy of early steroid withdrawal were determined in patients treated with either tacrolimus or microemulsion cyclosporin A (micro-CsA). The primary outcome was the proportion of patients who were steroid-free 1 year posttransplantation. From the seven Canadian adult liver transplant centers, 143 patients were randomly allocated oral treatment with either tacrolimus (n = 71) or micro-CsA (n = 72), together with corticosteroids and azathioprine. Eligibility criteria for steroid withdrawal included freedom from acute rejection for a minimum of 3 months, and prednisone ≤0.15 mg/kg/d. In eligible patients, the daily steroid dose was reduced by 2.5 mg each month until complete discontinuation was achieved. At 1 year after transplantation, 75% of the tacrolimus patients and 63% of the micro-CsA patients were steroid-free (P = .20). Of all of the patients who became eligible for steroid withdrawal, steroid discontinuation was achieved in over 80%. One-year patient survival was 97% with tacrolimus and 89% with micro-CsA (P = .052) . Graft survival was 97% and 86%, respectively (P = .017). The overall incidence of acute rejection during the first year was 35% with tacrolimus and 43% with micro-CsA (P = .26). There was no difference in survival, acute rejection, or rate of steroid withdrawal when adjusting for hepatitis C. All acute rejection episodes experienced during steroid withdrawal were steroid-responsive. Steroid-resistant rejection occurred in 5.6% of the tacrolimus and 9.7% of the micro-CsA patients. One patient, in the micro-CsA group, experienced refractory rejection. Chronic rejection was not observed in either group. The toxicity profiles were similar. Postoperative serum creatinine levels were similar, and dialysis was required in less than 10% of patients in each group. Infectious complications were similar in both groups. Neurotoxicity was a serious adverse event in 13% and 10% of patients receiving tacrolimus and micro-CsA, respectively. Early steroid withdrawal is safe and effective after liver transplantation using either tacrolimus plus azathioprine or micro-CsA plus azathioprine immunoprophylaxis. (Liver Transpl 2003;9:587-595.)
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号