Laftavi Mark R, Stephan Rabie, Stefanick Barbara, Kohli Romesh, Dagher Fadi, Applegate Mary, O'Keefe John, Pierce Drew, Rubino Andrea, Guzowski Haley, Leca Nicolae, Dayton Merril, Pankewycz Oleh
Departments of Surgery, SUNY-University at Buffalo, Buffalo General Hospital, Buffalo, NY, USA.
Surgery. 2005 Mar;137(3):364-71. doi: 10.1016/j.surg.2004.10.013.
Corticosteroid therapy after renal transplantation is associated with many adverse effects. Newer immunosuppressive agents may allow for safe and effective reductions in dose or early steroid withdrawal.
In this prospective, single-center clinical trial, 60 patients were randomized into 2 groups: control patients (n = 28), who received low doses of prednisone throughout, and study patients (n = 32), who were withdrawn from steroids 7 days posttransplant. Patients received a limited course of rabbit antilymphocyte globulin (rALG) induction therapy, tacrolimus (TAC), and mycophenolate mofetil (MMF). Patients were followed for clinical outcomes and renal function. Protocol biopsies were performed at 1, 6, and 12 months.
Clinical rejections occurred in 11% of controls and 13% of study patients. Renal function was well maintained and equivalent in both groups. In all, 111 protocol biopsies were performed without complications. Subclinical rejection was noted in only 2 protocol biopsies, and borderline changes were seen in 12 biopsies, all of which were distributed equally between both groups. Unsuspected acute TAC toxicity was seen in 8 biopsies. Protocol biopsies led to changes in therapy in 10% of patients. In both groups, serial protocol biopsies demonstrated increased allograft fibrosis over time, which was significant at 1 year in the steroid withdrawal group.
The immunosuppressive combination of rALG, TAC, and MMF prevents subclinical rejection and the need for high doses of steroids after transplantation. However, continual low-dose steroid therapy may aid in preventing chronic allograft fibrosis. Protocol biopsies help define the short-term and long-term risks of steroid withdrawal therapy.
肾移植后使用皮质类固醇疗法会带来许多不良反应。新型免疫抑制剂可能有助于安全有效地减少剂量或早期停用类固醇。
在这项前瞻性单中心临床试验中,60名患者被随机分为两组:对照组患者(n = 28),全程接受低剂量泼尼松治疗;研究组患者(n = 32),在移植后7天停用类固醇。患者接受了有限疗程的兔抗淋巴细胞球蛋白(rALG)诱导治疗、他克莫司(TAC)和霉酚酸酯(MMF)。对患者进行临床结局和肾功能随访。在1、6和12个月时进行方案规定的活检。
对照组11%的患者和研究组13%的患者发生临床排斥反应。两组肾功能均得到良好维持且相当。总共进行了111次方案规定的活检,无并发症发生。仅在2次方案规定的活检中发现亚临床排斥反应,12次活检出现临界变化,两组分布均匀。在8次活检中发现了未被怀疑的急性TAC毒性。方案规定的活检导致10%的患者治疗方案改变。两组中,系列方案规定的活检均显示随着时间推移移植肾纤维化增加,在停用类固醇组1年时差异显著。
rALG、TAC和MMF的免疫抑制组合可预防亚临床排斥反应以及移植后高剂量类固醇的使用需求。然而,持续低剂量类固醇治疗可能有助于预防慢性移植肾纤维化。方案规定的活检有助于明确停用类固醇治疗的短期和长期风险。