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优化免疫检查点抑制剂(阿替利珠单抗、纳武利尤单抗或帕博利珠单抗)治疗后肝移植的安全洗脱期。

Optimizing the Safe Washout Period for Liver Transplantation Following Immune Checkpoint Inhibitors with Atezolizumab, Nivolumab, or Pembrolizumab.

机构信息

Division of Transplantation Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, Taiwan; School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

Division of Transplantation Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, Taiwan; Institute of Public Health, National Yang Ming Chiao Tung University, Taipei, Taiwan; School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

出版信息

Transplant Proc. 2023 May;55(4):878-883. doi: 10.1016/j.transproceed.2023.03.064. Epub 2023 Apr 29.

Abstract

BACKGROUND

Using immune checkpoint inhibitors (ICIs) as a downstaging therapy for liver transplantation (LT) has improved outcomes for patients with advanced hepatocellular carcinoma (HCC). However, this therapy carries a risk of post-transplant graft rejection. The washout (WO) period between the last ICI dose and LT seems critical in preventing postoperative rejection. This study aimed to optimize the WO period by balancing tumor burden suppression and rejection prevention using ICIs before LT.

METHODS

We reviewed published case reports or series from March 2020 to December 2022 regarding LT for HCC after downstaging or bridge therapy with ICIs and included 4 of our cases. Most patients received atezolizumab, nivolumab, or pembrolizumab; these ICIs shared a half-life of around 28 days. Therefore, we excluded cases without definite WO period data and those using non-atezolizumab/nivolumab/pembrolizumab ICIs and ultimately enrolled 22 patients for analysis. We compared their clinical outcomes and estimated the rejection-free survival for every 0.5 half-life interval.

RESULTS

Most study subjects received nivolumab (n = 25). Six patients had severe rejections (nivolumab group, n = 5) and needed rescue management. Of the 6 cases, 1 patient died after rejection, and 2 underwent re-transplantation. The median WO period in these 6 patients was 22 days (IQR: 9-35 days). In addition, we found that a 1.5 half-life (42 days) was the shortest safe WO period associated with significant rejection-free survival (P = .005).

CONCLUSIONS

Our results showed that 42 days was the safest WO period before LT for HCC after ICI with atezolizumab, nivolumab, or pembrolizumab.

摘要

背景

免疫检查点抑制剂(ICI)作为肝移植(LT)的降期治疗方法,改善了晚期肝细胞癌(HCC)患者的预后。然而,这种治疗方法存在移植后移植物排斥的风险。ICI 末次剂量与 LT 之间的洗脱(WO)期似乎对预防术后排斥反应至关重要。本研究旨在通过在 LT 前使用 ICI 平衡肿瘤负担抑制和排斥反应预防,优化 WO 期。

方法

我们回顾了 2020 年 3 月至 2022 年 12 月期间发表的关于 HCC 患者在接受 ICI 降期或桥接治疗后进行 LT 的病例报告或系列研究,并纳入了我们的 4 例病例。大多数患者接受阿替利珠单抗、纳武利尤单抗或帕博利珠单抗治疗;这些 ICI 半衰期约为 28 天。因此,我们排除了没有明确 WO 期数据的病例和使用非阿替利珠单抗/纳武利尤单抗/帕博利珠单抗 ICI 的病例,并最终纳入 22 例患者进行分析。我们比较了他们的临床结果,并估计了每 0.5 个半衰期间隔的无排斥生存。

结果

大多数研究对象接受了纳武利尤单抗治疗(n=25)。6 例患者出现严重排斥反应(纳武利尤单抗组,n=5),需要进行抢救管理。这 6 例中有 1 例患者在排斥反应后死亡,2 例患者进行了再次移植。这 6 例患者的 WO 期中位数为 22 天(IQR:9-35 天)。此外,我们发现 1.5 个半衰期(42 天)是与显著无排斥生存相关的最短安全 WO 期(P=0.005)。

结论

我们的结果表明,在接受阿替利珠单抗、纳武利尤单抗或帕博利珠单抗治疗的 HCC 患者进行 LT 前,42 天是最安全的 WO 期。

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