Boots Johannes M M, Christiaans Maarten H L, Van Duijnhoven Elly M, Van Suylen Robert-Jan, Van Hooff Johannes P
Department of Nephrology, University Hospital Maastricht, PO Box 5800, 6202 AZ Maastricht, The Netherlands.
Transplantation. 2002 Dec 27;74(12):1703-9. doi: 10.1097/00007890-200212270-00011.
With tacrolimus-based immunosuppression, it appears safe to withdraw steroids 3 to 6 months after renal transplantation. We hypothesized whether steroids could also be safely withdrawn early after transplantation.
Sixty-two patients (first or second transplant, with no previous immunological failure, and current panel reactive human leucocyte antigen [HLA] antibodies [PRA]<50%), treated with tacrolimus, were prospectively randomized to stop steroids (10 mg prednisolone) after day 7 posttransplantation (stop group [STOP], n=28) or to gradually wean off steroids in 3 to 6 months (tapering group [TAP], n=34). Analyses were performed on an intention-to-treat basis.
After a median follow-up of 2.7 years, patient and graft survival were 97 and 90% and comparable between both groups (P =0.11 and P=0.13, respectively). The incidence of acute rejection was 29 (STOP) versus 33% (TAP) ( P=0.30). The time to the first rejection was a median of 35 days (STOP) versus 11 days (TAP) ( =0.19). The severity of the rejections (1997 Banff classification) was comparable (P =0.57). Creatinine clearance and proteinuria were similar (P >0.70). The incidence of infections was comparable ( P>0.10). The incidence of new-onset diabetes mellitus, defined as the use of antidiabetic medication, was 8.0 (STOP) versus 30.3% (TAP) (P =0.04). All cases occurred in the STOP group after 1 year, while all cases occurred in TAP in the first 4 months ( P<0.001).
Compared with tapering in 3 to 6 months, stopping steroids 1 week posttransplantation results in comparable patient and graft survival and in a similar incidence of acute rejections. The incidence of new-onset diabetes may be reduced. The immunosuppressive benefit of adding 10 mg prednisolone to tacrolimus seems to be limited.
在基于他克莫司的免疫抑制治疗中,肾移植后3至6个月停用类固醇似乎是安全的。我们推测移植后早期停用类固醇是否也安全。
62例接受他克莫司治疗的患者(首次或第二次移植,既往无免疫失败史,当前群体反应性人类白细胞抗原[HLA]抗体[PRA]<50%),前瞻性随机分为移植后第7天停用类固醇(10mg泼尼松龙)组(停药组[STOP],n = 28)或在3至6个月内逐渐减量停用类固醇组(减量组[TAP],n = 34)。分析基于意向性治疗原则进行。
中位随访2.7年后,患者和移植物存活率分别为97%和90%,两组之间具有可比性(P分别为0.11和0.13)。急性排斥反应发生率为29%(STOP组)对33%(TAP组)(P = 0.30)。首次排斥反应的时间中位数为35天(STOP组)对11天(TAP组)(P = 0.19)。排斥反应的严重程度(1997年班夫分类)具有可比性(P = 0.57)。肌酐清除率和蛋白尿相似(P>0.70)。感染发生率具有可比性(P>0.10)。新发糖尿病的发生率,定义为使用抗糖尿病药物,为8.0%(STOP组)对30.3%(TAP组)(P = 0.04)。所有病例均发生在STOP组1年后,而所有病例均发生在TAP组的前4个月(P<0.001)。
与在3至6个月内逐渐减量相比,移植后1周停用类固醇导致患者和移植物存活率相当,急性排斥反应发生率相似。新发糖尿病的发生率可能降低。在他克莫司基础上加用10mg泼尼松龙的免疫抑制益处似乎有限。