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.

Highlights

  • Melanoma incidence continues to rise, and unresectable metastatic melanoma is associated with high mortality [1]

  • Responses in advanced uveal melanoma have been very limited, so there remains no FDA-approved standard of care for metastatic uveal melanoma [8]

  • We present the case of a patient with metastatic uveal melanoma treated with percutaneous hepatic perfusion (PHP) followed by nivolumab who developed fulminant hepatic failure

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Summary

Introduction

Melanoma incidence continues to rise, and unresectable metastatic melanoma is associated with high mortality [1]. The development of immune checkpoint inhibitors, those targeting cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and programmed cell death-1 (PD-1), has dramatically improved long-term prognosis for patients with advanced cutaneous melanomas [4,5,6,7]. The incidence of grade 3 or 4 immune-related hepatitis is only seen in about 1% of patients, while fulminant hepatic failure has only rarely been reported [9, 13]. We present the case of a patient with metastatic uveal melanoma treated with PHP followed by nivolumab who developed fulminant hepatic failure. The patient was started on high-dose intravenous Solumedrol and liver function tests (LFTs), and symptoms initially improved during his first few hospital days. On the fourth hospital day (day 26 in Figure 1), his condition dramatically declined His LFTs rose rapidly to the thousands, resulting in fulminant liver failure. The fulminant hepatic failure was irreversible and led to death secondary to cardiorespiratory arrest

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