Immune-related encephalitis after immune checkpoint inhibitor therapy

免疫系统 脑炎 免疫学 医学 免疫检查点 病毒学 免疫疗法 病毒
作者
Monica Buckley,Aanika Balaji,Julie R. Brahmer,Laura C. Cappelli,William H. Sharfman,Ephraim J. Fuchs,Hyunseok Kang,Patrick M. Forde,Douglas E. Gladstone,Richard F. Ambinder,Ronan J. Kelly,Evan J. Lipson,Ivana Gojo,Edward J. Lee,Tory P. Johnson,Shiv Saidha,R. Llinás,Lyle W. Ostrow,Jarushka Naidoo,John C. Probasco
出处
期刊:Oncologist [AlphaMed Press]
卷期号:30 (1) 被引量:3
标识
DOI:10.1093/oncolo/oyae186
摘要

Immune checkpoint inhibitors (ICI) have revolutionized cancer treatment but can trigger immune-related encephalitis. We report one of the largest case series of patients with immune-related encephalitis and review of the literature. Retrospective series of patients with immune-related encephalitis and literature review. Fourteen patients with cancer treated with ICI (50% combination therapy) developed immune-related encephalitis. Diagnostic testing revealed cerebral spinal fluid (CSF) lymphocytic pleocytosis (85%) and elevated protein (69%), abnormal brain magnetic resonance imaging(MRI) (33%) or brain FDG-PET (25%), electroencephalogram (EEG) abnormalities (30%), and autoantibodies (31%). Encephalitis treatment included: corticosteroids (86%), intravenous immunoglobulin (IVIg) (36%), plasmapheresis (7%), and rituximab (29%). There were no deaths and 12 patients had significant recovery, although long-term complications were observed. All patients discontinued ICI. Longitudinal follow-up demonstrated anti-cancer response to ICI at 3 months (85%) and 6 months post-ICI initiation (77%). A literature review identified 132 patients with immune-related encephalitis. Most were treated with PD-1 inhibitors (18% combination). Common abnormalities included elevated CSF protein (84%) or pleocytosis (77%), abnormal brain MRI (65%), or autoantibodies (47%). Nearly all were treated with corticosteroids, many required additional therapy with IVIg (26%) or rituximab (12%). Most patients had clinical improvement (81%) but a minority (10%) had a clinical relapse after completing corticosteroid taper. ICIs were resumed in 7 patients (5%), with relapse in 3. Immune-related encephalitis is treatable and improves with corticosteroids in most cases but may require additional immunosuppression. Re-emergence of encephalitis is rare and does not typically result in adverse outcomes, and this should be considered in neurological immune-related adverse event management guidelines.

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