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单剂量阿替利珠单抗后发生急性肝衰竭,采用更新的RUCAM评估因果关系。

Acute Liver Failure following a Single Dose of Atezolizumab, as Assessed for Causality Using the Updated RUCAM.

作者信息

Tzadok Roie, Levy Sharon, Aouizerate Jessie, Shibolet Oren

机构信息

Department of Internal Medicine C, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Department of Gastroenterology and Hepatology, Tel Aviv Sourasky Medical Center and the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Case Rep Gastrointest Med. 2022 Mar 23;2022:5090200. doi: 10.1155/2022/5090200. eCollection 2022.


DOI:10.1155/2022/5090200
PMID:35368450
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8967548/
Abstract

Immune checkpoint inhibitors have become major therapeutic agents in oncology over the last few years. However, they are associated with a variety of potentially severe autoimmune phenomena. We present a patient with advanced adenocarcinoma of the lung, who presented with acute liver injury two weeks following his first treatment with atezolizumab, rapidly deteriorating to fulminant liver failure. A thorough evaluation of infectious, vascular, metabolic, and autoimmune etiologies did not yield any results. Liver pathology was nonspecific. Using RUCAM as a causality assessment method indicated probable connection between atezolizumab and liver damage. To our knowledge, this is the first documented report of a patient developing acute liver failure shortly after immune checkpoint inhibitor initiation.

摘要

在过去几年中,免疫检查点抑制剂已成为肿瘤学领域的主要治疗药物。然而,它们与多种潜在的严重自身免疫现象相关。我们报告一名晚期肺腺癌患者,在首次使用阿替利珠单抗治疗两周后出现急性肝损伤,并迅速恶化为暴发性肝衰竭。对感染、血管、代谢和自身免疫病因进行全面评估未得出任何结果。肝脏病理表现无特异性。使用RUCAM作为因果关系评估方法表明阿替利珠单抗与肝损伤之间可能存在关联。据我们所知,这是免疫检查点抑制剂开始使用后不久患者发生急性肝衰竭的首例文献报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc3/8967548/4eca06afc119/CRIGM2022-5090200.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc3/8967548/dd2af33c2481/CRIGM2022-5090200.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc3/8967548/4eca06afc119/CRIGM2022-5090200.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc3/8967548/dd2af33c2481/CRIGM2022-5090200.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc3/8967548/4eca06afc119/CRIGM2022-5090200.002.jpg

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[2]
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[3]
Checkpoint Inhibitor Induced Acute Liver Failure.

J Investig Med High Impact Case Rep. 2024

[4]
Human Leucocyte Antigen Genetics in Idiosyncratic Drug-Induced Liver Injury with Evidence Based on the Roussel Uclaf Causality Assessment Method.

Medicines (Basel). 2024-4-11

[5]
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[6]
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[7]
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本文引用的文献

[1]
Role of Corticosteroids in Drug-Induced Liver Injury. A Systematic Review.

Front Pharmacol. 2022-2-10

[2]
Anti-programmed cell death-1 and anti-programmed cell death ligand-1 immune-related liver diseases: from clinical pivotal studies to real-life experience.

Expert Opin Biol Ther. 2020-9

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Checkpoint inhibitor-induced liver injury: A novel form of liver disease emerging in the era of cancer immunotherapy.

Semin Diagn Pathol. 2019-7-24

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Association of Checkpoint Inhibitor-Induced Toxic Effects With Shared Cancer and Tissue Antigens in Non-Small Cell Lung Cancer.

JAMA Oncol. 2019-7-1

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JAMA Oncol. 2019-7-1

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J Hepatol. 2019-3-27

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J Oncol Pharm Pract. 2020-3

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World J Gastrointest Endosc. 2018-12-16

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Fatal Toxic Effects Associated With Immune Checkpoint Inhibitors: A Systematic Review and Meta-analysis.

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Immune checkpoint inhibitor-induced gastrointestinal and hepatic injury: pathologists' perspective.

J Clin Pathol. 2018-4-27

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