Ruggiero Rosanna, Stelitano Barbara, Fraenza Federica, di Mauro Gabriella, Scavone Cristina, Sportiello Liberata, Rafaniello Concetta, Di Napoli Raffaella, Danesi Romano, Del Re Marzia, Rossi Francesco, Capuano Annalisa
Campania Regional Centre for Pharmacovigilance and Pharmacoepidemiology, Naples, Italy.
Department of Experimental Medicine - Section of Pharmacology "L. Donatelli", University of Campania "Luigi Vanvitelli", Naples, Italy.
Front Oncol. 2022 Mar 15;12:824511. doi: 10.3389/fonc.2022.824511. eCollection 2022.
Immune checkpoint inhibitors (ICIs) are widely used improving clinical outcomes in many cancer patients. However, they can induce serious consequences, like neurological immune-related adverse drug reactions (NirADRs). Although these are rare complications, they can be serious with important impact on patients' quality of life. Our purpose is to describe these adverse events observed in the European clinical practice context. We carried out a descriptive analysis of individual case safety reports (ICSRs) related to ICIs collected until February 7, 2020, in the European spontaneous reporting database, EudraVigilance, and reported nervous disorders as suspect adverse drug reactions (ADRs). NirADRs were classified according to the Medical Dictionary for Regulatory Activities (MedDRA). In order to identify a hypothetical different reporting probability of the NirADR types between the ICI classes, we carried out a disproportionality analysis. The reporting odds ratio (ROR) with 95% CI was computed comparing the different ICI classes to each other based on their pharmacological target [the cytotoxic T-lymphocyte antigen-4 (CTLA-4), the programmed death-1 (PD-1) or its ligand (PD-L1)]. Finally, we researched in the literature the hypothesized mechanisms, which could explain the onset of these ICI-related neurological complications. Overall, we found 4,875 cases describing 6,429 ICI-related suspected NirADRs. ICI-related neurotoxicities include a wide range of central and peripheral events. These were mainly related to anti-PD-1 agents and occurred in male patients (59%). Our analysis confirmed a gender difference of NirADRs. Twenty-three percent of the events (comprising myasthenia gravis, neuropathy peripheral, and cerebral infarction) had unfavorable fallouts, including fatal outcome (7%). Majority of the NirADRs were categorized as "Neurological disorders NEC" HLGTs MedDRA (2,076; 32%). In 1,094 cases (22%), more NirADRs overlapped with other neurologic complications. An interesting overlapping of myasthenia gravis with myositis or myocarditis emerged. From our disproportionality analysis, an increased reporting probability of peripheral neuropathies and headaches emerged with ipilimumab when compared to anti-PD-1 and anti-PD-L1 agents. However, neuromuscular disorders were more probably reported with anti-PD-1. Several pathogenic mechanisms, including neuronal damage by T cells and autoantibodies and/or cytokine-mediated inflammation processes, have been hypothesized. However, the pathogenesis of these ICI-related complications is not completely understood. Considering the recent marketing authorizations of ICIs, further studies are strongly needed to monitor their neurologic safety profile.
免疫检查点抑制剂(ICIs)被广泛用于改善许多癌症患者的临床结局。然而,它们可能会引发严重后果,如神经免疫相关药物不良反应(NirADRs)。尽管这些是罕见的并发症,但可能很严重,会对患者的生活质量产生重大影响。我们的目的是描述在欧洲临床实践背景下观察到的这些不良事件。我们对截至2020年2月7日在欧洲自发报告数据库EudraVigilance中收集的与ICIs相关的个体病例安全报告(ICSRs)进行了描述性分析,并将神经障碍报告为可疑药物不良反应(ADRs)。NirADRs根据《监管活动医学词典》(MedDRA)进行分类。为了确定ICIs类别之间NirADR类型的假设不同报告概率,我们进行了不成比例分析。基于其药理学靶点[细胞毒性T淋巴细胞抗原4(CTLA-4)、程序性死亡1(PD-1)或其配体(PD-L1)],计算了不同ICIs类别相互比较的报告比值比(ROR)及其95%置信区间。最后,我们在文献中研究了可能解释这些与ICIs相关的神经并发症发生的假设机制。总体而言,我们发现4875例病例描述了6429例与ICIs相关的可疑NirADRs。与ICIs相关的神经毒性包括广泛的中枢和外周事件。这些主要与抗PD-1药物有关,且发生在男性患者中(59%)。我们的分析证实了NirADRs存在性别差异。23%的事件(包括重症肌无力、周围神经病变和脑梗死)产生了不良后果,包括致命结局(7%)。大多数NirADRs在MedDRA的“其他神经障碍”高级别组(HLGTs)中分类为“神经障碍,未另作说明”(2076例;32%)。在1094例病例(22%)中,更多的NirADRs与其他神经并发症重叠。出现了重症肌无力与肌炎或心肌炎有趣的重叠情况。从我们的不成比例分析中可以看出,与抗PD-1和抗PD-L1药物相比,使用伊匹单抗时周围神经病变和头痛的报告概率增加。然而,抗PD-1药物更有可能报告神经肌肉疾病。已经提出了几种致病机制,包括T细胞和自身抗体对神经元的损伤以及细胞因子介导的炎症过程。然而,这些与ICIs相关并发症的发病机制尚未完全了解。考虑到ICIs最近获得的上市许可,迫切需要进一步研究来监测其神经安全性概况。