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纳武单抗诱导的免疫性脑炎的临床特征、治疗及预后

Clinical features, treatment, and prognosis of nivolumab induced immune encephalitis.

作者信息

Wu Zhaoquan, Lei Haibo, Li Ronghui, Liu Xiang, Wang Chunjiang

机构信息

College of pharmacy, Changsha Medical University, No. 1501 Leifeng Avenue, Xiangjiang New District, Changsha, Hunan, 410219, China.

Hunan Provincial Key Laboratory of the Research and Development of Novel Pharmaceutical Preparations, Changsha Medical University, Changsha, Hunan, 410219, China.

出版信息

Invest New Drugs. 2025 Apr;43(2):293-300. doi: 10.1007/s10637-025-01522-x. Epub 2025 Mar 10.

Abstract

Immune encephalitis (IE) is an immune-mediated adverse events (irAEs) linked to nivolumab therapy, and its clinical characteristics remain unclear. This study aimed to analyze the clinical patterns of nivolumab-induced IE to inform diagnosis, treatment, and prevention strategies. We conducted a retrospective analysis of nivolumab-induced IE by reviewing case reports from the database until October 31, 2024. Among the 86 patients (53.5% male), the median age was 64 years (range 17, 83). The median time to the onset of IE was 38 days (range 4, 1430), and the median treatment cycle was 2 cycles (range 1, 18). The most prevalent symptoms included altered mental status (38.4%) and fever (37.2%). Cerebrospinal fluid analysis revealed elevated protein levels, normal glucose, and pleocytosis. Antineuronal antibodies were present in 29.1% of patients. MRI findings typically showed T2/FLAIR hyperintense signals in 52.3%. EEG results indicated diffuse slowing (16.3%). Following drug discontinuation and treatment, 86% of patients exhibited recovery or improvement, while 5.8% unfortunately succumbed to the condition. IE represents a rare yet severe irAEs associated with nivolumab. Clinicians must remain vigilant for signs of IE in patients undergoing nivolumab treatment. Diagnostic tests for nivolumab-induced IE generally do not reveal specific abnormalities. For individuals diagnosed with IE, it is crucial to initiate systemic steroid treatment without delay.

摘要

免疫性脑炎(IE)是一种与纳武利尤单抗治疗相关的免疫介导的不良事件(irAEs),其临床特征仍不明确。本研究旨在分析纳武利尤单抗诱导的IE的临床模式,为诊断、治疗和预防策略提供依据。我们通过回顾数据库中截至2024年10月31日的病例报告,对纳武利尤单抗诱导的IE进行了回顾性分析。在86例患者中(男性占53.5%),中位年龄为64岁(范围17至83岁)。IE发病的中位时间为38天(范围4至1430天),中位治疗周期为2个周期(范围1至18个周期)。最常见的症状包括精神状态改变(38.4%)和发热(37.2%)。脑脊液分析显示蛋白水平升高、葡萄糖正常和细胞增多。29.1%的患者存在抗神经元抗体。MRI检查结果通常显示52.3%的患者有T2/FLAIR高信号。脑电图结果显示弥漫性减慢(16.3%)。停药并治疗后,86%的患者病情恢复或改善,而不幸的是5.8%的患者死于该病。IE是一种与纳武利尤单抗相关的罕见但严重的irAEs。临床医生在纳武利尤单抗治疗的患者中必须对IE的迹象保持警惕。纳武利尤单抗诱导的IE的诊断检查一般不会发现特异性异常。对于诊断为IE的个体,及时启动全身类固醇治疗至关重要。

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