| Literature DB >> 33200345 |
Yuki Yoshikawa1,2, Michio Imamura1,2, Kenji Yamaoka1,2, Yumi Kosaka1,2, Eisuke Murakami1,2, Kei Morio1,2, Hatsue Fujino1,2, Takashi Nakahara1,2, Wataru Okamoto3, Masami Yamauchi1,2, Tomokazu Kawaoka1,2, Masataka Tsuge2,4, Akira Hiramatsu1,2, Clair Nelson Hayes1,2, Hiroshi Aikata1,2, Kazunori Fujitaka5, Kouji Arihiro6, Noboru Hattori5, Kazuaki Chayama7,8,9.
Abstract
Immune checkpoint inhibitor (ICI) therapy has potent anti-cancer effects but is associated with immune-related adverse events (irAEs). We present a case who developed secondary sclerosing cholangitis following treatment with nivolumab for non-small cell lung cancer who did not respond to immunosuppressive treatments and died of liver failure. A 75 year-old male with lung cancer who had been treated with nivolumab for non-small cell lung cancer developed Grade 3 liver injury with significant elevation of hepatobiliary enzymes. Magnetic resonance cholangiopancreatography (MRCP) revealed diffuse dilatation of the common bile duct and multifocal stenosis with prestenotic dilatation from the perihilar to intrahepatic bile duct, consistent with sclerosing cholangitis. Histological findings represented an infiltration of mainly CD8-positive T cells around the bile ducts in the liver. Despite treatments with ursodeoxycholic acid, prednisolone, and mycophenolate mofetil, the sclerosing cholangitis did not improve, and the patient died due to liver failure and aggravation of lung cancer. These findings suggest that immune checkpoint inhibitors may lead to resistance to immunosuppressive treatment as well as pose a risk of life-threatening sclerosing cholangitis.Entities:
Keywords: Magnetic resonance cholangiopancreatography; Nivolumab; Programmed cell death 1; Sclerosing cholangitis
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Year: 2020 PMID: 33200345 DOI: 10.1007/s12328-020-01287-1
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265