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免疫检查点抑制剂的肝脏免疫介导不良反应:真实世界经验分析

Hepatic immune-mediatedadverseeffects of immune checkpoint inhibitors: analysis of real-life experience.

作者信息

da Silva Joana Alves, Falcão Daniela, Cardoso Cláudia, Pires Ana Luísa, Araújo António, Castro-Poças Fernando

机构信息

Gastroenterology, Centro Hospitalar Universitário do Porto, Porto, Portugal.

Gastroenterology, Centro Hospitalar Universitário do Porto, Porto, Portugal.

出版信息

Ann Hepatol. 2021 Dec;26:100561. doi: 10.1016/j.aohep.2021.100561. Epub 2021 Oct 13.

Abstract

INTRODUCTION AND OBJECTIVES

Immune Checkpoint Inhibitors (ICI) have shifted the paradigm of cancer therapy treatment. Despite their efficacy, ICIs may induce immune-related adverse events (irAE), which can affect various organs, namely the liver. This study intends to perform a comprehensive clinical description of the hepatic irAEs associated with ICI in a Portuguese population of a tertiary hospital centre.

MATERIALS AND METHODS

A retrospective analysis of patients who developed immune-mediated liver injury (IMLI), among a cohort of patients treated with ICIs between March 15 of 2015 and December 15 of 2019 in a tertiary hospital. We used both Common Terminology Criteria for Adverse Events (CTCAE) and Drug-Induced Liver Injury Network (DILIN) criteria to define liver injury.

RESULTS

Among 151 patients, eight (5.3%) patients developed liver injury grade ≥3, of which five had hepatic metastasis. As such, only 3 cases were classified as IMLI. All IMLI presented with cholestasis pattern; the median duration from ICI initiation to IMLI was 84 days and/or 4 ICI cycles; one patient registered IMLI one month after nivolumab suspension; all were treated with steroids and one was successfully submitted to ICI re-challenge; a favourable outcome was seen in all patients; the median time to hepatic biochemistries normalization was 150 days. Among 10 patients with previous hepatic conditions, only one developed liver injury grade 2.

CONCLUSIONS

Clinically significant ICI-related hepatotoxicity was uncommon; Immune-mediated liver injury may present a cholestatic pattern predominance. There was a low rate of liver injury of any kind in patients with previous hepatic disease while on ICI.

摘要

引言与目的

免疫检查点抑制剂(ICI)已改变癌症治疗模式。尽管ICI疗效显著,但可能引发免疫相关不良事件(irAE),可累及多个器官,包括肝脏。本研究旨在对一家葡萄牙三级医院中心人群中与ICI相关的肝脏irAE进行全面临床描述。

材料与方法

对2015年3月15日至2019年12月15日在一家三级医院接受ICI治疗的患者队列中发生免疫介导性肝损伤(IMLI)的患者进行回顾性分析。我们使用不良事件通用术语标准(CTCAE)和药物性肝损伤网络(DILIN)标准来定义肝损伤。

结果

在151例患者中,8例(5.3%)患者发生≥3级肝损伤,其中5例有肝转移。因此,仅3例被归类为IMLI。所有IMLI均表现为胆汁淤积模式;从开始使用ICI至发生IMLI的中位时间为84天和/或4个ICI周期;1例患者在纳武单抗停药1个月后发生IMLI;所有患者均接受了类固醇治疗,1例成功接受了ICI再激发治疗;所有患者均预后良好;肝生化指标恢复正常的中位时间为150天。在10例既往有肝脏疾病的患者中,仅1例发生2级肝损伤。

结论

临床上具有显著意义的ICI相关肝毒性并不常见;免疫介导性肝损伤可能以胆汁淤积模式为主。既往有肝脏疾病的患者在使用ICI期间发生任何类型肝损伤的发生率较低。

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