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免疫检查点抑制剂诱导的炎性关节炎。

Immune checkpoint inhibitor-induced inflammatory arthritis.

作者信息

Fisher Benjamin A, Allard Andrew, Dubey Shirish, Mankia Kulveer, Pratt Arthur G, Pallan Lalit

机构信息

Rheumatology Research Group, Department of Inflammation and Ageing, School of Infection, Inflammation and Immunology, University of Birmingham, Birmingham, UK; Department of Rheumatology and NIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Royal National Hospital for Rheumatic Diseases, Royal United Hospitals Bath NHSFT, Bath BA1 3NG, UK.

出版信息

Clin Med (Lond). 2025 Aug 6;25(5):100496. doi: 10.1016/j.clinme.2025.100496.

DOI:10.1016/j.clinme.2025.100496
PMID:40774545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12391593/
Abstract

Immune checkpoint inhibitors (ICI) used for the treatment of malignancy are associated with immune-related adverse events, which include inflammatory arthritis. ICI-induced inflammatory arthritis (ICI-IA) is a new clinical entity that may lead to functional impairment and may be persistent even after ICI cessation. We discuss the clinical features, investigation and differential diagnosis. Management needs to consider the safety of immunosuppression in the context of the underlying cancer, and current practice will be further informed by ongoing clinical trials.

摘要

用于治疗恶性肿瘤的免疫检查点抑制剂(ICI)与免疫相关不良事件有关,其中包括炎性关节炎。ICI诱导的炎性关节炎(ICI-IA)是一种新的临床实体,可能导致功能障碍,甚至在停用ICI后仍可能持续存在。我们讨论了其临床特征、检查及鉴别诊断。管理需要在潜在癌症的背景下考虑免疫抑制的安全性,正在进行的临床试验将为当前的实践提供进一步的依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eb3/12391593/7cf7332b0dfd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eb3/12391593/7cf7332b0dfd/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eb3/12391593/7cf7332b0dfd/gr1.jpg

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本文引用的文献

1
Whole-body MRI in patients with arthralgia or inflammatory arthritis after exposure to immune checkpoint inhibitors: a single-centre prospective imaging study.免疫检查点抑制剂暴露后关节痛或炎性关节炎患者的全身MRI:一项单中心前瞻性影像学研究
Lancet Rheumatol. 2025 Jun 10. doi: 10.1016/S2665-9913(25)00061-X.
2
Chronicity of Immune Checkpoint Inhibitor-Associated Inflammatory Arthritis After Immunotherapy Discontinuation: Results From the Canadian Research Group of Rheumatology in Immuno-Oncology Database.免疫治疗停药后免疫检查点抑制剂相关炎性关节炎的慢性化:加拿大免疫肿瘤学风湿病研究组数据库的结果
ACR Open Rheumatol. 2025 Feb;7(2):e70002. doi: 10.1002/acr2.70002.
3
2024 EULAR points to consider on the initiation of targeted therapies in patients with inflammatory arthritis and a history of cancer.
2024年欧洲抗风湿病联盟关于炎性关节炎合并癌症病史患者开始使用靶向治疗的考虑要点
Ann Rheum Dis. 2024 Dec 20. doi: 10.1136/ard-2024-225982.
4
Corticosteroids for Immune-Related Adverse Events and Checkpoint Inhibitor Efficacy: Analysis of Six Clinical Trials.皮质类固醇类药物治疗免疫相关不良事件及检查点抑制剂疗效:六项临床试验分析。
J Clin Oncol. 2024 Nov;42(31):3713-3724. doi: 10.1200/JCO.24.00191. Epub 2024 Aug 7.
5
JAKing up immunity.激活免疫。
Science. 2024 Jun 21;384(6702):1303-1304. doi: 10.1126/science.adq1717. Epub 2024 Jun 20.
6
Rapid onset pembrolizumab-induced inflammatory arthritis diagnosed using musculoskeletal ultrasound.采用肌肉骨骼超声诊断快速发作的帕博利珠单抗诱导的炎症性关节炎。
BMJ Case Rep. 2024 Apr 24;17(4):e258706. doi: 10.1136/bcr-2023-258706.
7
Comparative safety and effectiveness of TNF inhibitors, IL6 inhibitors and methotrexate for the treatment of immune checkpoint inhibitor-associated arthritis.比较 TNF 抑制剂、IL6 抑制剂和甲氨蝶呤治疗免疫检查点抑制剂相关关节炎的安全性和有效性。
Ann Rheum Dis. 2023 Jul;82(7):920-926. doi: 10.1136/ard-2023-223885. Epub 2023 Apr 5.
8
Management of toxicities from immunotherapy: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up.免疫疗法毒性的管理:ESMO诊断、治疗及随访临床实践指南
Ann Oncol. 2022 Dec;33(12):1217-1238. doi: 10.1016/j.annonc.2022.10.001. Epub 2022 Oct 18.
9
Imaging Findings in Patients with Immune Checkpoint Inhibitor-Induced Arthritis.免疫检查点抑制剂诱导的关节炎患者的影像学表现
Diagnostics (Basel). 2022 Aug 13;12(8):1961. doi: 10.3390/diagnostics12081961.
10
Checkpoint Inhibition Reduces the Threshold for Drug-Specific T-Cell Priming and Increases the Incidence of Sulfasalazine Hypersensitivity.检查点抑制降低了药物特异性 T 细胞启动的阈值,并增加了柳氮磺胺吡啶过敏的发生率。
Toxicol Sci. 2022 Feb 28;186(1):58-69. doi: 10.1093/toxsci/kfab144.