Atezolizumab-associated encephalitis in metastatic lung adenocarcinoma: a case report.
Atezolizumab
Encephalitis
Immune checkpoint inhibitor
Immune-related adverse event
Lung adenocarcinoma
Programmed death ligand 1 inhibitor
Journal
Journal of medical case reports
ISSN: 1752-1947
Titre abrégé: J Med Case Rep
Pays: England
ID NLM: 101293382
Informations de publication
Date de publication:
04 Jul 2020
04 Jul 2020
Historique:
received:
05
03
2020
accepted:
25
05
2020
entrez:
5
7
2020
pubmed:
6
7
2020
medline:
30
3
2021
Statut:
epublish
Résumé
In recent years, immune checkpoint inhibitors have been widely used as a crucial therapy in malignant tumors. Immune checkpoint inhibitors can cause various autoimmune side effects called immune-related adverse events because they generate an exaggerated inflammatory response. Encephalitis associated with atezolizumab has rarely been reported as an immune-related adverse event. A case of encephalitis caused by treatment with atezolizumab is presented. A 56-year-old Japanese man with lung cancer previously treated with surgery and chemotherapy was admitted with high fever, consciousness disorder, and motor aphasia. His first atezolizumab treatment was 17 days earlier. Admission brain magnetic resonance imaging with gadolinium enhancement showed no abnormalities. Cerebrospinal fluid showed cell count 20/l, protein 166 mg/dl, glucose 73 mg/dl, and interleukin 6 82.9 pg/ml (normal< 8.7 pg/ml). Atezolizumab-induced encephalitis was diagnosed. His symptoms improved the day after steroid pulse therapy was started. Following steroid pulse therapy, oral prednisolone 30 mg was started and tapered. The cerebrospinal fluid findings normalized on day 14. He was discharged on day 16 without neurological sequelae. In this case of encephalitis associated with atezolizumab, prompt steroid pulse therapy led to a successful response, and the outcome was good. The cerebrospinal fluid level of interleukin 6 reflected the severity of the encephalitis well. Clinicians should be aware of the possibility of encephalitis after initiation of immune checkpoint inhibitors.
Sections du résumé
BACKGROUND
BACKGROUND
In recent years, immune checkpoint inhibitors have been widely used as a crucial therapy in malignant tumors. Immune checkpoint inhibitors can cause various autoimmune side effects called immune-related adverse events because they generate an exaggerated inflammatory response. Encephalitis associated with atezolizumab has rarely been reported as an immune-related adverse event. A case of encephalitis caused by treatment with atezolizumab is presented.
CASE PRESENTATION
METHODS
A 56-year-old Japanese man with lung cancer previously treated with surgery and chemotherapy was admitted with high fever, consciousness disorder, and motor aphasia. His first atezolizumab treatment was 17 days earlier. Admission brain magnetic resonance imaging with gadolinium enhancement showed no abnormalities. Cerebrospinal fluid showed cell count 20/l, protein 166 mg/dl, glucose 73 mg/dl, and interleukin 6 82.9 pg/ml (normal< 8.7 pg/ml). Atezolizumab-induced encephalitis was diagnosed. His symptoms improved the day after steroid pulse therapy was started. Following steroid pulse therapy, oral prednisolone 30 mg was started and tapered. The cerebrospinal fluid findings normalized on day 14. He was discharged on day 16 without neurological sequelae.
CONCLUSION
CONCLUSIONS
In this case of encephalitis associated with atezolizumab, prompt steroid pulse therapy led to a successful response, and the outcome was good. The cerebrospinal fluid level of interleukin 6 reflected the severity of the encephalitis well. Clinicians should be aware of the possibility of encephalitis after initiation of immune checkpoint inhibitors.
Identifiants
pubmed: 32620173
doi: 10.1186/s13256-020-02411-y
pii: 10.1186/s13256-020-02411-y
pmc: PMC7334840
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Immune Checkpoint Inhibitors
0
Interleukin-6
0
atezolizumab
52CMI0WC3Y
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
88Références
N Engl J Med. 2018 Jun 14;378(24):2288-2301
pubmed: 29863955
J Clin Oncol. 2018 Jun 10;36(17):1714-1768
pubmed: 29442540
Lancet. 2017 Jan 21;389(10066):255-265
pubmed: 27979383
Brain Res Bull. 2003 Aug 15;61(3):287-97
pubmed: 12909299
JAMA Neurol. 2016 Aug 1;73(8):928-33
pubmed: 27271951
Gynecol Oncol Rep. 2018 Mar 26;24:51-53
pubmed: 29915799
N Engl J Med. 2018 Jan 11;378(2):158-168
pubmed: 29320654
eNeurologicalSci. 2018 Dec 17;14:49-50
pubmed: 30619952
Clin Genitourin Cancer. 2017 Oct;15(5):e847-e849
pubmed: 28372981
SAGE Open Med Case Rep. 2018 Aug 02;6:2050313X18792422
pubmed: 30116528