Division of Thoracic Surgery, Department of Cardiothoracic Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Department of Pharmacy, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
Front Immunol. 2022 Jun 1;13:864545. doi: 10.3389/fimmu.2022.864545. eCollection 2022.
Induction therapy is used in about 80% of lung transplant centers and is increasing globally. Currently, there are no standards or guidelines for the use of induction therapy. At our institution, we have two induction strategies, basiliximab, and alemtuzumab. The goal of this manuscript is to share our experience and practice since this is an area of controversy.
We retrospectively reviewed 807 lung transplants performed at our institution between 2011 and 2020. Indications for the use of the basiliximab protocol were as follows: patients over the age of 70 years, history of cancer, hepatitis C virus or human immunodeficiency virus infection history, and cytomegalovirus or Epstein-Barr virus (donor positive/ recipient negative). In the absence of these clinical factors, the alemtuzumab protocol was used.
453 patients underwent alemtuzumab induction and 354 patients underwent basiliximab. There were significant differences in delayed chest closure (24.7% alemtuzumab vs 31.4% basiliximab, p = 0.037), grade 3 primary graft dysfunction observed within 72 hours (19.9% alemtuzumab vs 29.9% basiliximab, p = 0.002), postoperative hepatic dysfunction (8.8% alemtuzumab vs 14.7% basiliximab, p = 0.009), acute cellular rejection in first year (39.1% alemtuzumab vs 53.4% basiliximab, p < 0.001). The overall survival rate of the patients with alemtuzumab induction was significantly higher than those of the patients with basiliximab induction (5 years survival rate: 64.1% alemtuzumab vs 52.3%, basiliximab, p < 0.001). Multivariate Cox regression analysis confirmed lower 5-year survival for basiliximab induction (HR = 1.41, p = 0.02), recipient cytomegalovirus positive (HR = 1.49, p = 0.01), postoperative hepatic dysfunction (HR = 2.20, p < 0.001), and acute kidney injury requiring renal replacement therapy (HR = 2.27, p < 0.001).
In this single center retrospective review, there was a significant difference in survival rates between induction strategies. This outcome may be attributable to differences in recipient characteristics between the groups. However, the Alemtuzumab group experienced less episodes of acute cellular rejection within the first year.
诱导治疗约在 80%的肺移植中心使用,并且在全球范围内呈上升趋势。目前,尚无诱导治疗使用的标准或指南。在我们机构,我们有两种诱导策略,巴利昔单抗和阿仑单抗。本文的目的是分享我们的经验和实践,因为这是一个有争议的领域。
我们回顾性分析了 2011 年至 2020 年在我们机构进行的 807 例肺移植。使用巴利昔单抗方案的指征如下:年龄超过 70 岁、癌症史、丙型肝炎病毒或人类免疫缺陷病毒感染史、巨细胞病毒或 EBV(供体阳性/受体阴性)。在没有这些临床因素的情况下,使用阿仑单抗方案。
453 例患者接受阿仑单抗诱导,354 例患者接受巴利昔单抗诱导。阿仑单抗组延迟关胸(24.7% vs 31.4%,p = 0.037)、72 小时内 3 级原发性移植物功能障碍(19.9% vs 29.9%,p = 0.002)、术后肝功能障碍(8.8% vs 14.7%,p = 0.009)、第一年急性细胞排斥反应(39.1% vs 53.4%,p < 0.001)发生率显著较高。阿仑单抗诱导患者的总生存率明显高于巴利昔单抗诱导患者(5 年生存率:64.1% vs 52.3%,p < 0.001)。多变量 Cox 回归分析证实巴利昔单抗诱导的 5 年生存率较低(HR = 1.41,p = 0.02)、受体巨细胞病毒阳性(HR = 1.49,p = 0.01)、术后肝功能障碍(HR = 2.20,p < 0.001)和需要肾脏替代治疗的急性肾损伤(HR = 2.27,p < 0.001)。
在这项单中心回顾性研究中,诱导策略之间的生存率存在显著差异。这种结果可能归因于两组受体特征的差异。然而,阿仑单抗组在第一年发生急性细胞排斥反应的次数较少。