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本文引用的文献

1
Polymyalgia rheumatica and giant cell arteritis induced by immune checkpoint inhibitors: A systematic literature review highlighting differences from the idiopathic forms.免疫检查点抑制剂诱导的巨细胞动脉炎和风湿性多肌痛:系统文献综述强调与特发性疾病的差异。
Autoimmun Rev. 2024 Jul-Aug;23(7-8):103589. doi: 10.1016/j.autrev.2024.103589. Epub 2024 Aug 6.
2
Checkpoint inhibitor-related myasthenia-myocarditis-myositis overlap syndrome in the orbit.眼眶中与检查点抑制剂相关的重症肌无力-心肌炎-肌炎重叠综合征
Orbit. 2025 Apr;44(2):200-206. doi: 10.1080/01676830.2024.2351519. Epub 2024 May 26.
3
Defining D-irAEs: consensus-based disease definitions for the diagnosis of dermatologic adverse events from immune checkpoint inhibitor therapy.定义 D-irAEs:基于共识的免疫检查点抑制剂治疗相关皮肤不良反应诊断的疾病定义。
J Immunother Cancer. 2024 Apr 10;12(4):e007675. doi: 10.1136/jitc-2023-007675.
4
Impact of Immune Checkpoint Inhibitors on the Course of Multiple Sclerosis.免疫检查点抑制剂对多发性硬化病程的影响。
Neurol Neuroimmunol Neuroinflamm. 2024 Mar;11(2):e200202. doi: 10.1212/NXI.0000000000200202. Epub 2024 Feb 12.
5
Survival Among Veterans Receiving Steroids for Immune-Related Adverse Events After Immune Checkpoint Inhibitor Therapy.免疫检查点抑制剂治疗后免疫相关不良事件接受类固醇治疗的退伍军人的存活率。
JAMA Netw Open. 2023 Oct 2;6(10):e2340695. doi: 10.1001/jamanetworkopen.2023.40695.
6
Treatment of steroid-refractory immune checkpoint inhibitor-induced intestinal pseudo-obstruction with infliximab.英夫利昔单抗治疗类固醇难治性免疫检查点抑制剂诱导的肠道假性梗阻
Rev Esp Enferm Dig. 2024 Jul;116(7):383-384. doi: 10.17235/reed.2023.9796/2023.
7
Concurrent immune checkpoint inhibition and selective immunosuppressive therapy in patients with immune-related enterocolitis.免疫相关肠炎患者的免疫检查点抑制和选择性免疫抑制治疗的联合应用。
J Immunother Cancer. 2023 Jun;11(6). doi: 10.1136/jitc-2023-007195.
8
Pigmentary retinopathy associated with immune therapy for advanced cutaneous melanoma.与晚期皮肤黑色素瘤免疫治疗相关的色素性视网膜病变
Am J Ophthalmol Case Rep. 2023 Apr 18;30:101849. doi: 10.1016/j.ajoc.2023.101849. eCollection 2023 Jun.
9
Ophthalmic immune-related adverse events associated with immune checkpoint inhibitors.与免疫检查点抑制剂相关的眼部免疫相关不良反应。
Front Immunol. 2023 Mar 23;14:1130238. doi: 10.3389/fimmu.2023.1130238. eCollection 2023.
10
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.

免疫检查点抑制剂眼部免疫相关不良事件的共识性疾病定义。

Consensus disease definitions for ophthalmic immune-related adverse events of immune checkpoint inhibitors.

作者信息

Chang Eileen L, Liu Renee, Keyhanian Kiandokht, Huynh Katie, Berkenstock Meghan, Bhatti M Tariq, Chen John J, Chodosh James, Costello Fiona, Dalvin Lauren A, DeLott Lindsey B, Dinkin Marc, Egan Robert A, Fraser Clare L, Freitag Suzanne K, Gangaputra Sapna, Gordon Lynn K, Guidon Amanda C, Johnson Douglas B, Kombo Ninani, Kramer Michal, Lee Andrew G, Levy Michael, Lobo-Chan Anne-Marie, Mantopoulos Dimosthenis, Papaliodis George, Pless Misha, Pimkina Julia, Rubin Krista M, Sen H Nida, Shariff Afreen, Subramanian Prem S, Tsui Edmund, Yoon Michael K, McDunn Jon, Rine Johnathan, Reynolds Kerry L, Sobrin Lucia, Chwalisz Bart K

机构信息

Department of Ophthalmology, Mass Eye and Ear, Boston, Massachusetts, USA.

Department of Ophthalmology, Weill Cornell Medical College, New York, New York, USA.

出版信息

J Immunother Cancer. 2025 Apr 8;13(4):e011049. doi: 10.1136/jitc-2024-011049.

DOI:10.1136/jitc-2024-011049
PMID:40199607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11979595/
Abstract

Ophthalmic immune-related adverse events (Eye-irAEs) from immune checkpoint inhibitors can cause visual morbidity. The absence of standardized definitions for Eye-irAEs not only impedes the development of evidence-based treatments but also progress in translational research. The objective of this study was to develop consensus guidance for an approach to Eye-irAEs.Four ophthalmic physicians (uveitis specialists and neuro-ophthalmologists) drafted Eye-irAE consensus guidance and definitions, which were reviewed by the multidisciplinary Eye-irAE definition panel. The panel was divided into Group A (Neuro-ophthalmology/Orbital Disease) and Group B (Uveitis/Ocular Surface Disease). A modified Delphi consensus process was used, with two rounds of anonymous ratings by panelists and two meetings to discuss areas of controversy. For each disorder, five diagnostic components were evaluated: symptoms, examination findings, laboratory studies/imaging findings, diagnostic criteria, and treatment. Panelists rated content for usability, appropriateness and accuracy on 9-point scales in electronic surveys and provided free-text comments. Aggregated survey responses were incorporated into revised definitions. Consensus was based on numeric ratings using the RAND Corporation/ University of California Los Angeles Health Services Utilization Study (RAND/UCLA) Appropriateness Method with prespecified definitions.29 panelists from 25 academic medical centers voted on 114 rating scales (66 neuro-ophthalmic/orbital disease components, 48 uveitis/ocular surface disease components); of these, 86.3% (57/66) in Group A and 89.6% (43/48) in Group B reached first-round consensus. After revisions, all items except 6.1% (4/66) in Group A and 1.6% (1/60) in Group B received second-round consensus. Consensus definitions were achieved for 10/11 neuro-ophthalmic/orbital disorders: optic neuritis, inflammatory optic disc edema, arteritic ischemic optic neuropathy, optic perineuritis, orbital inflammation, thyroid eye disease-like orbital inflammation, cavernous sinus syndrome, oculomotor mononeuritis, trochlear mononeuritis, and abducens mononeuritis. Consensus definitions were achieved for 9/10 uveitis/ocular surface disorders: anterior uveitis, intermediate uveitis, posterior uveitis, panuveitis, Vogt-Koyanagi-Harada-like syndrome, sarcoidosis-like syndrome, acute macular neuroretinopathy, dry eye disease, and scleritis.These disease definitions establish a standardized classification for Eye-irAE, highlighting differences between irAEs and other inflammatory disorders. Importantly, diagnostic certainty does not always align directly with the need to treat as an Eye-irAE. Given the consensus from this representative panel group, it is anticipated the definitions will be used broadly across clinical and research settings.

摘要

免疫检查点抑制剂引起的眼科免疫相关不良事件(眼部免疫相关不良反应)可导致视力损害。眼部免疫相关不良反应缺乏标准化定义,不仅阻碍了循证治疗的发展,也影响了转化研究的进展。本研究的目的是制定眼部免疫相关不良反应处理方法的共识指南。四位眼科医生(葡萄膜炎专家和神经眼科医生)起草了眼部免疫相关不良反应的共识指南和定义,由多学科眼部免疫相关不良反应定义小组进行审核。该小组分为A组(神经眼科/眼眶疾病)和B组(葡萄膜炎/眼表疾病)。采用改良的德尔菲共识法,小组成员进行两轮匿名评分,并召开两次会议讨论有争议的领域。对于每种疾病,评估五个诊断要素:症状、检查结果、实验室检查/影像学检查结果、诊断标准和治疗。小组成员在电子调查中以9分制对内容的可用性、适宜性和准确性进行评分,并提供自由文本评论。汇总的调查回复被纳入修订后的定义中。共识基于使用兰德公司/加利福尼亚大学洛杉矶分校卫生服务利用研究(RAND/UCLA)适宜性方法及预先指定定义的数值评分。来自25个学术医学中心的29名小组成员对114个评分量表进行了投票(66个神经眼科/眼眶疾病要素,48个葡萄膜炎/眼表疾病要素);其中,A组86.3%(57/66)和B组89.6%(43/48)达成第一轮共识。修订后,A组除6.1%(4/66)、B组除1.6%(1/60)的所有项目均达成第二轮共识。对于10/11种神经眼科/眼眶疾病达成了共识定义:视神经炎、炎性视盘水肿、动脉炎性缺血性视神经病变、视神经周围炎、眼眶炎症、甲状腺眼病样眼眶炎症、海绵窦综合征、动眼神经单神经炎、滑车神经单神经炎和展神经单神经炎。对于9/10种葡萄膜炎/眼表疾病达成了共识定义:前葡萄膜炎、中间葡萄膜炎、后葡萄膜炎、全葡萄膜炎、Vogt-小柳-原田样综合征、结节病样综合征、急性黄斑神经视网膜病变、干眼症和巩膜炎。这些疾病定义为眼部免疫相关不良反应建立了标准化分类,突出了免疫相关不良反应与其他炎症性疾病的差异。重要的是,诊断的确定性并不总是与作为眼部免疫相关不良反应进行治疗的必要性直接相关。鉴于该代表性小组达成的共识,预计这些定义将在临床和研究环境中广泛应用。