Neurological adverse events associated with immune checkpoint inhibitors: Review of the literature

被引:0
|
作者
Cuzzubbo, S. [1 ,2 ]
Javeri, F. [1 ]
Tissier, M. [1 ]
Roumi, A. [1 ]
Barlog, C. [1 ,2 ]
Doridam, J. [1 ,2 ]
Lebbe, C. [3 ,4 ]
Belin, C. [1 ,2 ]
Ursu, R. [1 ,2 ]
Carpentier, A. F. [1 ,2 ]
机构
[1] Hop Avicenne, AP HP, Serv Neurol, Bobigny, France
[2] Univ Paris 13, UFR Sante Med & Biol Humaine, Bobigny, France
[3] Univ Paris Diderot, Sorbonne Paris Cite, Hop St Louis, APHP,Dermatol Dept,INSERM,U976, Paris, France
[4] Univ Paris Diderot, Sorbonne Paris Cite, Hop St Louis, APHP,CIC Dept,INSERM,U976, Paris, France
关键词
Anti-PD1; Anti-CTLA4; Immune checkpoint inhibitors; Neurological adverse events; LONG-TERM SAFETY; PHASE-II TRIAL; PRETREATED ADVANCED MELANOMA; RESISTANT PROSTATE-CANCER; GUILLAIN-BARRE-SYNDROME; CELL LUNG-CANCER; SINGLE-ARM; OPEN-LABEL; CTLA4; BLOCKADE; IPILIMUMAB TREATMENT;
D O I
10.1016/j.ejca.2016.12:001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune checkpoint inhibitors (ICIs) targeting CTLA4 and PD1 constitute a promising class of cancer treatment but are associated with several immune-related disorders. We here review the literature reporting neurological adverse events (nAEs) associated with ICIs. A systematic search of literature, up to February 2016, mentioning nAEs in patients treated with ICIs was conducted. Eligible studies included case reports and prospective trials. One case seen in our ward was also added. Within the 59 clinical trials (totalling 9208 patients) analysed, the overall incidence of nAEs was 3.8% with anti-CTLA4 antibodies, 6.1% with anti-PD1 antibodies, and 12.0% with the combination of both. The clinical spectrum of neurological disorders was highly heterogeneous. Most of these nAEs were grade 1-2 and consisted of non-specific symptoms such as headache (55%). The incidence of high grade nAEs was below 1% for all types of treatment. Headaches, encephalopathies and meningitis were the most commonly reported (21%, 19% and 15%, respectively). Among the 27 case reports, the most common nAEs were encephalopathies, meningoradiculoneuritis, Guillain-Barre like syndromes and myasthenic syndromes. The median time of nAEs onset was 6 weeks. In most cases, drug interruption and steroids led to neurological recovery, even in conditions where steroids are not usually recommended such as Guillain-Barre syndrome. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:1 / 8
页数:8
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