| Literature DB >> 28317087 |
Hisato Kawakami1, Junko Tanizaki2, Kaoru Tanaka2, Koji Haratani2, Hidetoshi Hayashi2, Masayuki Takeda2, Ken Kamata3, Mamoru Takenaka3, Masatomo Kimura4, Takaaki Chikugo4, Takao Sato5, Masatoshi Kudo3, Akihiko Ito4, Kazuhiko Nakagawa2.
Abstract
Background Nivolumab demonstrates promising efficacy for the treatment of non-small cell lung cancer and other malignancies. The clinical benefit of nivolumab, however, may be hampered by specific immune-related adverse events (irAEs), and little is known regarding nivolumab-related cholangitis. Methods A computerized search of our clinical database identified 3 metastatic non-small cell lung cancer patients with nivolumab-related cholangitis. All patients were treated with intravenous nivolumab monotherapy (3.0 mg/kg) every 2 weeks until disease progression or irAEs occurred. Clinical data regarding the duration of nivolumab treatment, symptoms, laboratory abnormalities, pathological findings of liver parenchyma biopsy specimens, and management of nivolumab-related cholangitis were analyzed. Results Our analysis revealed that nivolumab-related cholangitis was characterized by (1) localized extrahepatic bile duct dilation without obstruction; (2) diffuse hypertrophy of the extrahepatic bile duct wall; (3) a dominant increase in the biliary tract enzymes alkaline phosphatase and gamma-glutamyl transpeptidase relative to the hepatic enzymes aspartate and alanine aminotransferase; (4) normal or reduced levels of the serum immunological markers antinuclear antibody, antimitochondrial antibody, smooth muscle antibody, and immunoglobulin G4; (5) the pathological finding of biliary tract cluster of differentiation 8-positive T cell infiltration from liver biopsy; and (6) a moderate to poor response to steroid therapy. Conclusions Nivolumab-related cholangitis is associated with distinct imaging and clinicopathological features that distinguish it from acute cholangitis of common etiologies and other immune-related cholangitis. Further studies are warranted to establish the optimal management of patients with this irAE.Entities:
Keywords: Cholangitis; Immune-related adverse event; Nivolumab monotherapy; Programmed death-1
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Year: 2017 PMID: 28317087 DOI: 10.1007/s10637-017-0453-0
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850