University of Chicago Medical Center, Chicago, Illinois, USA.
Am J Respir Crit Care Med. 2011 Feb 1;183(3):379-87. doi: 10.1164/rccm.201005-0775OC. Epub 2010 Sep 10.
Lung transplantation has evolved into a life-saving therapy for select patients with end-stage lung diseases. However, long-term survival remains limited because of chronic rejection. Sirolimus is beneficial in preventing cardiac rejection and may decrease rejection after lung transplantation.
To determine the potential benefit versus risk of sirolimus in lung transplantation.
We conducted a multicenter randomized, open label controlled trial comparing sirolimus (SIR) with azathioprine (AZA) in a tacrolimus-based immunosuppressive regimen in lung transplantation. The primary end point was the incidence of acute rejection at 1 year after transplantation between the two study groups.
One hundred eighty-one patients were randomized to be included in this study. At 1 year after transplantation, there was no significant difference in the incidence of grade A acute rejection between the two study groups. Similarly, the incidence of chronic rejection and graft survival was no different between the two study groups. Cytomegalovirus infection was decreased in the SIR arm compared with the AZA arm (relative risk, 0.67 [95% confidence interval, 0.55, 0.82]; P < 0.01). There was a higher rate of adverse events leading to early discontinuation of SIR (64%) compared with AZA (49%) during the course of this study.
Sirolimus, an mTOR inhibitor, did not decrease the incidence of acute rejection at 1 year compared with azathioprine in lung transplantation. These results differ from previous results in cardiac and renal transplantation and emphasize the need for multicenter randomized controlled trials in lung transplantation. Clinical trial registered with www.clinicaltrials.gov (NCT 00321906).
肺移植已成为治疗终末期肺部疾病患者的一种救生疗法。然而,由于慢性排斥反应,长期存活率仍然有限。西罗莫司在预防心脏排斥反应方面有益,并可能减少肺移植后的排斥反应。
确定西罗莫司在肺移植中的潜在益处与风险。
我们进行了一项多中心随机、开放标签对照试验,比较了西罗莫司(SIR)与他克莫司为基础的免疫抑制方案中的硫唑嘌呤(AZA)在肺移植中的应用。主要终点是两组研究患者在移植后 1 年内急性排斥反应的发生率。
181 例患者随机分组纳入本研究。移植后 1 年,两组患者的 A 级急性排斥反应发生率无显著差异。同样,两组患者的慢性排斥反应发生率和移植物存活率也无差异。与 AZA 组相比,SIR 组巨细胞病毒感染减少(相对风险,0.67 [95%置信区间,0.55, 0.82];P < 0.01)。在本研究过程中,因不良事件导致 SIR 早期停药的发生率(64%)高于 AZA 组(49%)。
与硫唑嘌呤相比,mTOR 抑制剂西罗莫司在肺移植后 1 年内并未降低急性排斥反应的发生率。这些结果与心脏和肾脏移植中的先前结果不同,强调需要在肺移植中进行多中心随机对照试验。临床试验在 www.clinicaltrials.gov 注册(NCT 00321906)。