免疫检查点抑制剂肌病:癌症免疫疗法的双刃剑

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY
Neurology Pub Date : 2024-12-10 Epub Date: 2024-11-08 DOI:10.1212/WNL.0000000000210031
Grayson Beecher, Iago Pinal-Fernandez, Andrew L Mammen, Teerin Liewluck
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引用次数: 0

摘要

免疫检查点抑制剂(ICI)疗法彻底改变了多种恶性肿瘤的治疗方法,提高了患者的生存率。这些单克隆抗体靶向免疫检查点,包括细胞毒性T淋巴细胞相关蛋白4(ipilimumab和tremelimumab)、程序性死亡1(nivolumab、pembrolizumab、cemiplimab和dostarlimab)、程序性死亡配体1(atezolizumab、avevelumab和durvalumab)和淋巴细胞活化基因3(relatlimab),并有效增强了针对肿瘤细胞的免疫反应。然而,松开免疫系统的 "刹车 "也会带来后果,即可能影响任何器官的免疫相关不良事件(irAEs)。神经系统irAEs占所有irAEs的1%-3%,其中免疫介导的肌病(ICI肌病)是最常见的表现。最近的大型患者系列研究和系统综述确定了 ICI 肌病的主要特征,并强调了对 ICI 肌病的新认识。ICI 肌病的特征是急性或亚急性起病的眼球和/或四肢近端无力,伴有或不伴有呼吸功能不全和心肌炎。肌酸激酶升高很常见。伴有或不伴有呼吸衰竭的眼球后肌无力可能会被误认为是神经肌肉接头紊乱,尤其是因为多达 40% 的患者体内存在乙酰胆碱受体抗体;然而,即使是严重无力的患者也往往没有神经肌肉传导缺陷的电诊断证据,这突出表明肌病过程才是这些表现背后的驱动力。肌肉组织病理学通常表现为多灶性坏死和再生纤维簇的独特特征,从而将 ICI 肌病与其他自身免疫性肌病区分开来。转录组分析发现了 ICI 肌病的不同亚群,揭示了受影响肌肉组织中不同程度的 1 型和 2 型干扰素通路激活,以及白细胞介素 (IL)-6 通路的显著上调。这一发现为通过使用抑制干扰素通路和靶向 IL-6 或其受体的疗法进行干预提供了一个前景广阔的途径。尽管以皮质类固醇为主要治疗手段的免疫调节疗法在临床上有所改善,但死亡率仍然很高,尤其是伴有心肌炎或呼吸衰竭需要插管的患者,死亡率高达 50%。停用 ICI 可导致癌症进展和死亡,因此需要改进 ICI 再挑战的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune Checkpoint Inhibitor Myopathy: The Double-Edged Sword of Cancer Immunotherapy.

Immune checkpoint inhibitor (ICI) therapy has revolutionized the treatment of several malignancies, with improved survival. These monoclonal antibodies target immune checkpoints, including cytotoxic T-lymphocyte-associated protein 4 (ipilimumab and tremelimumab), programmed death 1 (nivolumab, pembrolizumab, cemiplimab, and dostarlimab), programmed death ligand 1 (atezolizumab, avelumab, and durvalumab), and lymphocyte activation gene 3 (relatlimab), and effectively augment the immune response against tumor cells. Releasing the brakes on the immune system has consequences, however, in the form of immune-related adverse events (irAEs), which may affect any organ. Neurologic irAEs represent 1%-3% of all irAEs, with immune-mediated myopathy (ICI myopathy) being the most common manifestation. Recent large patient series and systematic reviews have established the key features and highlighted new insights into ICI myopathy. ICI myopathy is characterized by an acute or subacute onset of oculobulbar and/or proximal limb weakness, with or without associated respiratory insufficiency and myocarditis. Creatine kinase elevation is common. Oculobulbar presentations with or without respiratory failure may be misattributed to neuromuscular junction disorders, particularly because acetylcholine receptor antibodies are present in up to 40% of patients; however, an electrodiagnostic evidence of a defect of neuromuscular transmission is often absent even in patients with severe weakness, highlighting that the myopathic process is the driving force behind these presentations. Muscle histopathology commonly demonstrates a unique signature of multifocal clusters of necrotic and regenerating fibers, differentiating ICI myopathy from other autoimmune myopathies. Transcriptomic analysis has uncovered distinct subgroups within ICI myopathy, revealing varying degrees of type 1 and type 2 interferon pathway activation alongside notable upregulation of the interleukin (IL)-6 pathway in affected muscle tissue. This discovery presents a promising avenue for intervention through the use of therapies that suppress the interferon pathway and target IL-6 or its receptor. Despite clinical improvements with immunomodulatory therapy, with corticosteroids the mainstay of treatment, mortality remains high, particularly in those with associated myocarditis or respiratory failure requiring intubation, where mortality occurs in up to 50%. ICI withdrawal can lead to cancer progression and death, highlighting a need for improved approaches to ICI rechallenge, performed in limited patients with variable success to date.

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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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