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一名转移性葡萄膜黑色素瘤患者在经皮肝灌注和纳武单抗化学饱和后发生暴发性肝衰竭。

Fulminant Hepatic Failure after Chemosaturation with Percutaneous Hepatic Perfusion and Nivolumab in a Patient with Metastatic Uveal Melanoma.

作者信息

Teal Lindsey, Yorio Jeffrey

机构信息

The University of Texas at Austin Dell Medical School, Austin, Texas, USA.

Texas Oncology, Austin, Texas, USA.

出版信息

Case Rep Oncol Med. 2021 Mar 29;2021:8870334. doi: 10.1155/2021/8870334. eCollection 2021.

Abstract

Immune checkpoint inhibitors, such as nivolumab, a programmed death receptor-1 (PD-1) inhibitor, have dramatically improved the treatment of advanced melanomas. Chemosaturation with percutaneous hepatic perfusion (PHP) delivers chemotherapy in high doses directly to the liver and is a potentially effective treatment modality in metastatic uveal melanoma with liver metastases. Its safety and effectiveness have not been studied in patients also receiving immunotherapy. A 46-year-old male with a history of uveal melanoma of the right eye was found to have liver metastases. He was treated with PHP using high-dose melphalan for 6 months with a partial response followed by progression. Two months after his last PHP treatment, the patient was started on nivolumab. After two doses of nivolumab, the patient developed severe hepatitis that progressed to fulminant hepatic failure and death despite treatment with high-dose corticosteroids and mycophenolate mofetil. Nivolumab and other immune checkpoint inhibitors have been effective in treating advanced melanoma and extending life. However, there are serious immune adverse events that can occur. While hepatitis after taking nivolumab has been documented, fulminant hepatic failure is rare. We believe that prior PHP treatment contributed to the severity of the hepatitis and, ultimately, fulminant hepatic failure. To our knowledge, this is the only case of fulminant hepatic failure secondary to a checkpoint inhibitor with preceding PHP. Specific precautions should be made in patients who have been exposed to PHP in the past, and further studies should be done to assess the safety of using checkpoint inhibitors after PHP.

摘要

免疫检查点抑制剂,如程序性死亡受体1(PD-1)抑制剂纳武单抗,已显著改善了晚期黑色素瘤的治疗。经皮肝灌注化疗(PHP)通过高剂量直接向肝脏输送化疗药物,是转移性葡萄膜黑色素瘤伴肝转移的一种潜在有效治疗方式。其安全性和有效性尚未在同时接受免疫治疗的患者中进行研究。一名46岁有右眼葡萄膜黑色素瘤病史的男性被发现有肝转移。他接受了使用高剂量美法仑的PHP治疗6个月,有部分缓解,随后病情进展。在他最后一次PHP治疗两个月后,患者开始使用纳武单抗。在使用两剂纳武单抗后,患者出现严重肝炎,尽管接受了高剂量皮质类固醇和霉酚酸酯治疗,仍进展为暴发性肝衰竭并死亡。纳武单抗和其他免疫检查点抑制剂在治疗晚期黑色素瘤和延长生命方面已取得成效。然而,可能会发生严重的免疫不良事件。虽然服用纳武单抗后的肝炎已有记录,但暴发性肝衰竭很少见。我们认为先前的PHP治疗导致了肝炎的严重程度,最终导致暴发性肝衰竭。据我们所知,这是唯一一例在接受PHP治疗后继发于检查点抑制剂的暴发性肝衰竭病例。对于过去接触过PHP的患者应采取特定预防措施,并且应进一步开展研究以评估PHP治疗后使用检查点抑制剂的安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f13/8024064/3e62a4136075/CRIONM2021-8870334.001.jpg

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