Response to immunotherapy in anti‐IgLON5 disease: A systematic review

The aim of this study was to evaluate the frequency of response to immunotherapy in patients with anti‐IgLON5 disease through a systematic review of the literature. MEDLINE and Embase databases were searched for studies that included patients with anti‐IgLON5 disease who received immunotherapy (IT)....

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Veröffentlicht in:Acta neurologica Scandinavica 2020-04, Vol.141 (4), p.263-270
Hauptverfasser: Cabezudo‐García, Pablo, Mena‐Vázquez, Natalia, Estivill Torrús, Guillermo, Serrano‐Castro, Pedro
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container_issue 4
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container_title Acta neurologica Scandinavica
container_volume 141
creator Cabezudo‐García, Pablo
Mena‐Vázquez, Natalia
Estivill Torrús, Guillermo
Serrano‐Castro, Pedro
description The aim of this study was to evaluate the frequency of response to immunotherapy in patients with anti‐IgLON5 disease through a systematic review of the literature. MEDLINE and Embase databases were searched for studies that included patients with anti‐IgLON5 disease who received immunotherapy (IT). Review inclusion criteria were met by 18 studies. The main study variable was response to IT, defined as the frequency of patients with an improvement greater than mild in at least one of the main symptoms defined by the clinical phenotype. Data were also gathered on the rate of response to last follow‐up, the line(s) of IT received, the administration of monotherapy or combination therapy, and clinical and analytical characteristics. Selected studies included a total of 46 patients. A response to IT was observed in 20 (43.4%) and the presence of response to last follow‐up in 15 (32.6%). Response was achieved more frequently with combination therapy vs monotherapy (14/21 [66.6%] vs 7/22 [31.8%]) and second‐line therapy vs first‐line therapy (7/13 [53.8%] vs 15/46 [32.6%]). The response rate by drug was 34.2% (12/35) for steroids, 42.8% (9/21) for IVIg, 46% (7/15) for PLEX, 100% (5/5) for AZA and 75% (3/4) for MMF. Factors associated with a response to IT included the cognitive impairment and non‐classical phenotypes, presence of HLA‐DQB1*05:01 without HLA‐DRB1*10:01 and cerebral spinal fluid inflammation. Patients with anti‐IgLON5 disease respond to IT, and this response is associated with certain clinical and analytical characteristics of the patients. Also rate of response seems higher with second‐line and combination treatment. However, the quality of available studies is inadequate to allow definitive conclusions to be drawn.
doi_str_mv 10.1111/ane.13207
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source Wiley Online Library Journals Frontfile Complete
subjects anti‐IgLON5 disease
Cerebrospinal fluid
Cognitive ability
Drb1 protein
Histocompatibility antigen HLA
IgLON5
Immunoglobulins
Immunotherapy
Intravenous administration
Literature reviews
Patients
Phenotypes
Steroid hormones
Systematic review
treatment
title Response to immunotherapy in anti‐IgLON5 disease: A systematic review
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