Gassmann Dimitri, Weiler Stefan, Mertens Joachim C, Reiner Cäcilia S, Vrugt Bart, Nägeli Mirjam, Mangana Joanna, Müllhaupt Beat, Jenni Fabienne, Misselwitz Benjamin
Department of Internal Medicine, University Hospital Zurich and University of Zurich, Zürich, Switzerland.
Department of Clinical Pharmacology and Toxicology, University Hospital Zurich and University of Zurich, Zürich, Switzerland.
Transplant Direct. 2018 Jul 20;4(8):e376. doi: 10.1097/TXD.0000000000000814. eCollection 2018 Aug.
Orthotopic liver transplantation (OLT) is a potential curative treatment in patients with hepatocellular carcinoma (HCC); however, treatment options for recurrent HCC after OLT are limited. Immune checkpoint inhibitors, such as nivolumab, an inhibitor of programmed cell death protein 1, have been successfully used for metastatic HCC but data on safety of nivolumab following solid organ transplantation are limited.
We report a 53-year-old woman with HCC who was treated with OLT. After 2 years, HCC recurred. Initial treatment with sorafenib was discontinued due to side effects and disease progression. Progressive HCC in the lung and lymph nodes was subsequently treated with nivolumab. One week after the first nivolumab dose, rapid progressive liver dysfunction was noted. Liver biopsy revealed severe cellular graft rejection prompting treatment with intravenous steroids and tacrolimus. Liver function continued to decline, leading to severe coagulopathy. The patient succumbed to intracranial hemorrhage.
A systematic PubMed search revealed 29 cases treated with a checkpoint inhibitor following solid organ transplantation. Loss of graft was described in 4 (36%) of 11 cases with OLT and in 7 (54%) of 13 cases after kidney transplantation. However, cases with favorable outcome were also described. Eighteen cases with adverse events were identified upon searching the World Health Organization database VigiBase, including 2 cases with fatal outcome in liver transplant recipients due to graft loss.
Experience with checkpoint inhibitors in solid organ transplant recipients is limited. Published cases so far suggest severe risks for graft loss as high as 36% to 54%.
原位肝移植(OLT)是肝细胞癌(HCC)患者潜在的治愈性治疗方法;然而,OLT术后复发性HCC的治疗选择有限。免疫检查点抑制剂,如程序性细胞死亡蛋白1抑制剂纳武单抗,已成功用于转移性HCC,但关于实体器官移植后纳武单抗安全性的数据有限。
我们报告一名53岁的HCC女性患者接受了OLT治疗。2年后,HCC复发。由于副作用和疾病进展,索拉非尼的初始治疗中断。随后,肺部和淋巴结进展性HCC接受了纳武单抗治疗。首次使用纳武单抗剂量一周后,发现肝功能迅速进行性减退。肝活检显示严重的细胞移植排斥反应,促使给予静脉类固醇和他克莫司治疗。肝功能持续下降,导致严重凝血功能障碍。患者死于颅内出血。
PubMed系统检索显示,29例实体器官移植后接受检查点抑制剂治疗的病例。11例OLT患者中有4例(36%)和13例肾移植后患者中有7例(54%)出现移植物丢失。然而,也有预后良好的病例报道。在搜索世界卫生组织数据库VigiBase时,确定了18例不良事件病例,包括2例肝移植受者因移植物丢失导致的致命结果。
实体器官移植受者使用检查点抑制剂的经验有限。迄今为止发表的病例表明,移植物丢失的严重风险高达36%至54%。