1 Department of Surgery, Regensburg University Hospital, Regensburg, Germany. 2 Department of General and Visceral Surgery, Frankfurt University Hospital, Goethe-University Frankfurt/Main, Frankfurt/Main, Germany. 3 Department of Anesthesiology, Regensburg University Hospital, Regensburg, Germany.
Transplantation. 2015 Dec;99(12):2565-75. doi: 10.1097/TP.0000000000000779.
Renal impairment and high model of end-stage liver disease scores before liver transplantation (LT) are increasingly common.
This was a single-arm, 2-step prospective trial of bottom-up calcineurin inhibitor (CNI)-free de novo immunosuppressive treatment (mycofenolate mofetil, steroids, basiliximab) with delayed introduction of sirolimus in patients with renal impairment. Primary endpoint was immunologic safety assessed by the incidence of steroid-resistant rejection within the first 30 days after liver transplantation.
Twenty-seven patients were included with a median age of 56 years and labMELD of 28. Baseline glomerular filtration rate was 38 (Cockroft-Gault) and 24 mL/min (modification of diet in renal disease). No steroid-resistant rejections occurred within 30 days. Incidence of biopsy proven acute rejection was 18.5%. Sirolimus was started on day 10 (range, day 1 to day 48). The rate switched to CNI treatment by 1 year was 44%; 1-year overall survival was 93%. Renal function improved significantly, reflected by a Δglomerular filtration rate of 31 mL/min from baseline to 1 year (P = 0.006). Per protocol analysis revealed freedom from CNI, but not presence of sirolimus within the first 30 days, as critical for renal recovery.
Initial de novo CNI-free immunosuppressive bottom-up treatment is safe in selected patient groups. The critical period for relevant recovery of renal function seems to be the early period (first 30 days), independent from presence of sirolimus.
在肝移植(LT)前,肾功能损害和高终末期肝病模型评分越来越常见。
这是一项单臂、两步前瞻性试验,采用自下而上的钙调神经磷酸酶抑制剂(CNI)免费的新型免疫抑制治疗(霉酚酸酯、类固醇、巴利昔单抗),并在肾功能损害患者中延迟引入西罗莫司。主要终点是通过肝移植后 30 天内类固醇耐药排斥反应的发生率评估免疫安全性。
27 例患者纳入研究,中位年龄为 56 岁,实验室 MELD 为 28。基线肾小球滤过率为 38(Cockroft-Gault)和 24ml/min(肾脏疾病饮食改良)。30 天内无类固醇耐药排斥反应发生。活检证实急性排斥反应发生率为 18.5%。西罗莫司于第 10 天(范围:第 1 天至第 48 天)开始使用。1 年内转换为 CNI 治疗的比例为 44%;1 年总生存率为 93%。肾功能显著改善,从基线到 1 年肾小球滤过率增加了 31ml/min(P=0.006)。根据方案分析显示,在最初的 30 天内,无 CNI 且无西罗莫司的情况下,肾功能恢复是关键。
在选定的患者群体中,最初的新型 CNI 免费免疫抑制自下而上治疗是安全的。肾功能恢复的关键时期似乎是早期(前 30 天),与西罗莫司的存在无关。