Zimmerman Michael A, Trotter James F, Wachs Michael, Bak Tom, Campsen Jeffrey, Skibba Afshin, Kam Igal
Division of Transplant Surgery, University of Colorado Health Sciences Center, Denver, CO 80045, USA.
Liver Transpl. 2008 May;14(5):633-8. doi: 10.1002/lt.21420.
Experience with sirolimus (SRL)-based immunosuppression following orthotopic liver transplantation (OLT) is rapidly accumulating. In combination with calcineurin inhibitors (CNIs), SRL may reduce the incidence of acute rejection and lower overall required drug levels. This study sought to quantify long-term outcome following OLT in patients with cirrhosis and concomitant hepatocellular carcinoma (HCC) who were treated with an SRL-based regimen as a primary therapy. From January 2000 to June 2007, 97 patients underwent OLT for end-stage liver disease and HCC at the University of Colorado Health Sciences Center. Of those, 45 patients received SRL, in addition to CNIs, as a component of their primary immunosuppression regimen post-OLT. Conversely, 52 patients received the standard immunosuppression regimen including CNIs, mycophenolate mofetil, and corticosteroids. The 2 treatment groups were compared with respect to the following variables: age, gender, tumor stage by explant, grade, size, presence of vascular invasion, focality, Child's class, baseline creatinine, and warm and cold ischemic times. The 2 groups were comparable by all factors save for cold ischemic time, which was significantly longer in the CNI-treated group. Overall survival at 1 and 5 years post-OLT for patients treated with SRL was 95.5% and 78.8%, respectively. Conversely, survival in patients treated with CNIs exclusively at the same time intervals was 83% and 62%. Although there was no difference in the incidence of major complications, the SRL group experienced a modest improvement in renal function. Cumulatively, these data suggest a potential survival benefit with SRL-based therapy in patients undergoing OLT for end-stage liver disease and concomitant malignancy.
原位肝移植(OLT)后基于西罗莫司(SRL)的免疫抑制经验正在迅速积累。与钙调神经磷酸酶抑制剂(CNI)联合使用时,SRL可能会降低急性排斥反应的发生率并降低总体所需药物水平。本研究旨在量化以SRL为基础方案作为主要治疗方法的肝硬化合并肝细胞癌(HCC)患者OLT后的长期结局。2000年1月至2007年6月,97例患者在科罗拉多大学健康科学中心因终末期肝病和HCC接受了OLT。其中,45例患者在OLT后接受了SRL加CNI作为其主要免疫抑制方案的一部分。相反,52例患者接受了包括CNI、霉酚酸酯和皮质类固醇的标准免疫抑制方案。比较了两个治疗组在以下变量方面的情况:年龄、性别、移植肝肿瘤分期、分级、大小、血管侵犯情况、病灶情况、Child分级、基线肌酐以及热缺血和冷缺血时间。除冷缺血时间外,两组在所有因素方面均具有可比性,CNI治疗组的冷缺血时间明显更长。接受SRL治疗患者OLT后1年和5年总体生存率分别为95.5%和78.8%。相反,仅接受CNI治疗患者在相同时间间隔的生存率分别为83%和62%。虽然主要并发症的发生率没有差异,但SRL组的肾功能有适度改善。总体而言,这些数据表明,对于因终末期肝病和合并恶性肿瘤而接受OLT的患者,基于SRL的治疗可能具有生存益处。