Titre
EEG findings in CART T associated neurotoxicity: clinical and radiological correlations.
Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
Auteur(s)
Beuchat, I
Auteure/Auteur
Danish, H
Auteure/Auteur
Rubin, DB
Auteure/Auteur
Jacobson, C
Auteure/Auteur
Robertson, M
Auteure/Auteur
Vaitkevicius, H
Auteure/Auteur
Lee, JW
Auteure/Auteur
Liens vers les personnes
Liens vers les unités
Statut éditorial
Publié
Date de publication
2021-07
Peer-reviewed
Oui
Langue
anglais
Résumé
Background
While EEG is frequently reported as abnormal after CAR T cell therapy, its clinical significance remains unclear. We aim to systematically describe EEG features in a large single center cohort and correlate them with clinical and radiological findings.
Methods
We retrospectively identified patients undergoing CAR T cell therapy who had continuous EEG. Neurotoxicity grades, detailed neurological symptoms and brain MRI or FDG-PET were obtained. Correlation between clinical and radiological findings and EEG features were assessed.
Results
In 81 patients with median neurotoxicity grade 3 (IQR 2-3), diffuse EEG background slowing was the most common finding and correlated with neurotoxicity severity (p<0.001). A total of 42 patients had rhythmic or periodic patterns, 16 of them within the ictal-interical-continuum (IIC), 5 with clinical seizures, and 3 with only electrographic seizures. Focal EEG abnormalities, consisting of lateralized periodic discharges (LPD,n=1), lateralized rhythmic delta activity (LRDA, n=6) or focal slowing (n=19), were found in 22 patients. All patients with LRDA, LPD and 10/19 patients with focal slowing had focal clinical symptoms concordant with these EEG abnormalities. In addition, these focal EEG changes often correlated with PET hypometabolism or MRI hypoperfusion, in absence of a structural lesion.
Conclusion
In adult patients experiencing neurotoxicity after CAR T cell infusion, EEG degree of background disorganization correlated with neurotoxicity severity. IIC patterns and focal EEG abnormalities are frequent and often correlate with focal clinical symptoms and with PET-hypometabolism/MRI-hypoperfusion, without structural lesion. The etiology of these findings remains to be elucidated.
While EEG is frequently reported as abnormal after CAR T cell therapy, its clinical significance remains unclear. We aim to systematically describe EEG features in a large single center cohort and correlate them with clinical and radiological findings.
Methods
We retrospectively identified patients undergoing CAR T cell therapy who had continuous EEG. Neurotoxicity grades, detailed neurological symptoms and brain MRI or FDG-PET were obtained. Correlation between clinical and radiological findings and EEG features were assessed.
Results
In 81 patients with median neurotoxicity grade 3 (IQR 2-3), diffuse EEG background slowing was the most common finding and correlated with neurotoxicity severity (p<0.001). A total of 42 patients had rhythmic or periodic patterns, 16 of them within the ictal-interical-continuum (IIC), 5 with clinical seizures, and 3 with only electrographic seizures. Focal EEG abnormalities, consisting of lateralized periodic discharges (LPD,n=1), lateralized rhythmic delta activity (LRDA, n=6) or focal slowing (n=19), were found in 22 patients. All patients with LRDA, LPD and 10/19 patients with focal slowing had focal clinical symptoms concordant with these EEG abnormalities. In addition, these focal EEG changes often correlated with PET hypometabolism or MRI hypoperfusion, in absence of a structural lesion.
Conclusion
In adult patients experiencing neurotoxicity after CAR T cell infusion, EEG degree of background disorganization correlated with neurotoxicity severity. IIC patterns and focal EEG abnormalities are frequent and often correlate with focal clinical symptoms and with PET-hypometabolism/MRI-hypoperfusion, without structural lesion. The etiology of these findings remains to be elucidated.
PID Serval
serval:BIB_281019FFC5C0
PMID
URL éditeur
Date de création
2022-06-16T14:21:49.678Z
Date de création dans IRIS
2025-05-20T19:43:25Z
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Nom
Neuro_Onco.pdf
Version du manuscrit
postprint
Taille
11.52 MB
Format
Adobe PDF
PID Serval
serval:BIB_281019FFC5C0.P001
URN
urn:nbn:ch:serval-BIB_281019FFC5C03
Somme de contrôle
(MD5):c949c5a5ae23fe37cb185158e82bbfb0