A case report on severe nivolumab-induced adverse events similar to primary sclerosing cholangitis refractory to immunosuppressive therapy.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
11 Jun 2021
Historique:
received: 30 01 2021
accepted: 15 04 2021
entrez: 11 6 2021
pubmed: 12 6 2021
medline: 25 6 2021
Statut: ppublish

Résumé

Immune checkpoint inhibitors (ICIs), particularly anti-PD-1 antibody, have dramatically changed cancer treatment; however, fatal immune-related adverse events (irAEs) can develop. Here, we describe a severe case of sclerosing cholangitis-like irAE. We report the use of 3 immunosuppressive agents that resulted in the death of the patient due to treatment inefficacy. According to a postmarketing study of nivolumab, the frequency of ICI-related sclerosing cholangitis is 0.27% and that of ICI-related cholangitis is 0.20%. There have been 4 case reports of sclerosing cholangitis-like irAE, with imaging findings, including typical intrahepatic bile duct beaded constriction in primary sclerosing cholangitis. Treatment starts with prednisolone and is combined with an immunosuppressant in refractory cases. There are no reports of severe cases that ultimately led to death. The patient is a 64-year-old male with Stage IV squamous cell lung carcinoma; he was hospitalized with abdominal pain and elevation of aspartate transaminase and alanine transaminase, approximately 4 months after ICI administration was suspended. This occurred because the patient treated with nivolumab as the second-line chemotherapy and developed type 1 diabetes mellitus after 11 courses. A grade 3 increase in bilirubin was observed and he was diagnosed with sclerosing cholangitis, based on magnetic resonance cholangiopancreatography imaging and pathological findings of the liver and bile duct. Prednisolone, mycophenolate mofetil, and tacrolimus combination therapy was administered. The treatment was difficult and failed. He died from liver failure 8 months after diagnosis. In this case, hepatitis and cholangitis, mainly alanine transaminase-dominant liver disorder, developed in the early stages of irAEs. Although he showed some improvement after prednisolone administration, bilirubin levels began rising again, and sclerosing cholangitis did not improve even with the use of 3 immunosuppressive agents recommended by the ESMO Clinical Practice Guidelines for immune-related hepatotoxicity management. Although the antitumor effect showed a complete response, liver failure led to death. This is the first case report on the ineffectiveness of triple immunosuppressant combination therapy recommended by the guidelines for immune-related hepatotoxicity. It is necessary to develop more appropriate treatment for severe sclerosing cholangitis-like irAE based on the robust evidence.

Identifiants

pubmed: 34114983
doi: 10.1097/MD.0000000000025774
pii: 00005792-202106110-00006
pmc: PMC8202549
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0
Immunosuppressive Agents 0
Nivolumab 31YO63LBSN
Prednisolone 9PHQ9Y1OLM
Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2
Tacrolimus WM0HAQ4WNM

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e25774

Informations de copyright

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

The authors have no funding and conflicts of interest to disclose.

Références

Hossein Borghaei DO, Luis Paz-Ares MD, Leora Horn MD, et al. Nivolumab versus docetaxel in advanced nonsquamous non–small-cell lung cancer. N Engl J Med 2015;373:1627–39.
The Reports of Safety and Information on Proper Use. Ono Pharmaceutical Co., Ltd. Available at: https://www.opdivo.jp/basic-info/report/ [access date January 20, 2020].
Haanen JBAG, Carbonnel F, Robert C, et al. Management of toxicities from immunotherapy: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2017;28: (Suppl 4): iv119–42.
Gelsomino F, Vitale G, D’Errico A, et al. Nivolumab-induced cholangitic liver disease: a novel form of serious liver injury. Ann Oncol 2017;28:671–2.
Kawakami H, Tanizaki J, Tanaka K, et al. Imaging and clinicopathological features of nivolumab-related cholangitis in patients with non-small cell lung cancer. Invest New Drugs 2017;35:529–36.
Sawada K, Shonaka T, Nishikawa Y, et al. Successful treatment of nivolumab-related cholangitis with prednisolone: a case report and review of the literature. Intern Med 2019;58:1747–52.
Kashima J, Okuma Y, Shimizuguchi R, et al. Bile duct obstruction in a patient treated with nivolumab as second-line chemotherapy for advanced non-small-cell lung cancer: a case report. Cancer Immunol Immunother 2018;67:61–5.
Doherty GJ, Duckworth AM, Davies SE, et al. Severe steroid-resistant anti-PD1 T-cell checkpoint inhibitor-induced hepatotoxicity driven by biliary injury. ESMO Open 2017;2:e000268.
Kuraoka N, Hara K, Terai S, et al. Peroral cholangioscopy of nivolumab-related (induced) ulcerative cholangitis in a patient with non-small cell lung cancer. Endoscopy 2018;50:E259–61.
Cho JH, Sun JM, Lee SH, et al. Late-onset cholecystitis with cholangitis after avelumab treatment in non-small cell lung cancer. J Thorac Oncol 2018;13:e34–6.
Zachou K, Gatselis N, Papadamou G, et al. Mycophenolate for the treatment of autoimmune hepatitis: prospective assessment of its efficacy and safety for induction and maintenance of remission in a large cohort of treatment-naïve patients. J Hepatol 2011;55:636–46.
Hlivko JT, Shiffman ML, Stravitz RT, et al. A single center review of the use of mycophenolate mofetil in the treatment of autoimmune hepatitis. Clin Gastroenterol Hepatol 2008;6:1036–40.
Chmiel KD, Suan D, Liddle C, et al. Resolution of severe ipilimumab-induced hepatitis after antithymocyte globulin therapy. J Clin Oncol 2011;29:e237–40.
Spänkuch I, Gassenmaier M, Tampouri I, et al. Severe hepatitis under combined immunotherapy: resolution under corticosteroids plus anti-thymocyte immunoglobulins. Eur J Cancer 2017;81:203–5.
Noda-Narita S, Mizuno S, Noguchi S, et al. Development of mild drug-induced sclerosing cholangitis after discontinuation of nivolumab. Eur J Cancer 2019;107:93–6.
Kono M, Sakurai T, Okamoto K, et al. Efficacy and safety of chemotherapy following anti-PD-1 antibody therapy for gastric cancer: a case of sclerosing cholangitis. Intern Med 2019;58:1263–6.
Ogawa K, Kamimura K, Terai S. Antiprogrammed cell death-1 immunotherapy-related secondary sclerosing cholangitis. Hepatology 2019;69:914–6.
Koya Y, Shibata M, Shinohara N, et al. Secondary sclerosing cholangitis with hemobilia induced by pembrolizumab: case report and review of published work. Hepatol Res 2019;49:950–6.
Doycheva I, Watt KD, Gulamhusein AF. Autoimmune hepatitis: current and future therapeutic options. Liver Int 2019;39:1002–13.
Terziroli Beretta-Piccoli B, Mieli-Vergani G, Vergani D. Autoimmune hepatitis: standard treatment and systematic review of alternative treatments. World J Gastroenterol 2017;23:6030–48.
Efe C, Hagström H, Ytting H, et al. Efficacy and safety of mycophenolate mofetil and tacrolimus as second-line therapy for patients with autoimmune hepatitis. Clin Gastroenterol Hepatol 2017;15:1950–6.
Zhang X, Ran Y, Wang K, et al. Incidence and risk of hepatic toxicities with PD-1 inhibitors in cancer patients: a meta-analysis. Drug Des Devel Ther 2016;10:3153–61.
Eigentler TK, Hassel JC, Berking C, et al. Diagnosis, monitoring and management of immune-related adverse drug reactions of anti-PD-1 antibody therapy. Cancer Treat Rev 2016;45:07–18.
Simonelli M, Di Tommaso L, Baretti M, et al. Pathological characterization of nivolumab-related liver injury in a patient with glioblastoma. Immunotherapy 2016;8:1363–9.
De Martin E, Michot JM, Papouin B, et al. Characterization of liver injury induced by cancer immunotherapy using immune checkpoint inhibitors. J Hepatol 2018;68:1181–90.

Auteurs

Yuya Hirasawa (Y)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Kiyoshi Yoshimura (K)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.
Department of Clinical Immuno-Oncology, Clinical Research Institute of Clinical Pharmacology and Therapeutics, Showa University.

Hiroto Matsui (H)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Yutaro Kubota (Y)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Hiroo Ishida (H)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Jun Arai (J)

Division of Gastroenterology, Department of Medicine.

Masashi Sakaki (M)

Division of Gastroenterology, Department of Medicine.

Nao Oguro (N)

Division of Rheumatology, Department of Medicine.

Midori Shida (M)

Department of Clinical Immuno-Oncology, Clinical Research Institute of Clinical Pharmacology and Therapeutics, Showa University.

Makoto Taniguchi (M)

Department of Clinical Immuno-Oncology, Clinical Research Institute of Clinical Pharmacology and Therapeutics, Showa University.

Kazuyuki Hamada (K)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Hirotsugu Ariizumi (H)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Tomoyuki Ishiguro (T)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Ryotaro Ohkuma (R)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Takehiko Sambe (T)

Division of Clinical Pharmacology, Department of Pharmacology, Showa University School of Medicine.

Atsushi Horiike (A)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

Chiyo K Imamura (CK)

Advanced Cancer Translational Research Institute, Showa University.

Eisuke Shiozawa (E)

Department of Pathology and Laboratory Medicine, Showa University School of Medicine.

Satoshi Wada (S)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.
Department of Clinical Diagnostic Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University.

Junji Tsurutani (J)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.
Advanced Cancer Translational Research Institute, Showa University.

Sanju Iwamoto (S)

Division of Physiology and Pathology, Department of Pharmacology, Toxicology and Therapeutics, Showa University School of Pharmacy.

Naoki Uchida (N)

Division of Clinical Pharmacology, Department of Pharmacology, Showa University School of Medicine.

Yuji Kiuchi (Y)

Division of Medical Pharmacology, Department of Pharmacology, Showa University School of Medicine.

Genshu Tate (G)

Department of Pathology and Laboratory Medicine, Showa University School of Medicine.

Shinichi Kobayashi (S)

Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Takuya Tsunoda (T)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine.

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