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Giant Cell Temporal Arteritis Followed by Severe Encephalopathy Induced by Immunotherapy in a Patient with Metastatic Renal Cell Carcinoma Achieving Durable Partial Response: A Case Report
O. Fiala, M. Tkadlecová, K. Pivovarčíková, J. Baxa, P. Stránský, D. Šiková, M. Hora, J. Fínek
Status neindexováno Jazyk angličtina Země Švýcarsko
Typ dokumentu kazuistiky, časopisecké články
NLK
Directory of Open Access Journals
od 2008
Free Medical Journals
od 2008
PubMed Central
od 2008
Europe PubMed Central
od 2008
ProQuest Central
od 2017-01-01
Open Access Digital Library
od 2008-01-01
Open Access Digital Library
od 2008-01-01
Health & Medicine (ProQuest)
od 2017-01-01
Karger Open Access
od 2008-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2008
PubMed
39474545
DOI
10.1159/000540660
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
INTRODUCTION: Combined immuno-oncology (IO) regimens are the cornerstone of the current front-line systemic therapy for metastatic renal cell carcinoma (mRCC). Despite the fact that combined IO regimens show high efficacy, they are often accompanied by a wide spectrum of immune-related adverse effects (irAEs). CASE PRESENTATION: We describe a case of rare irAEs manifested as giant cell temporal arteritis (GCA) followed by severe encephalopathy occurring after continuing immunotherapy in a 66-year-old man with mRCC receiving a combination of ipilimumab and nivolumab in the first line of systemic therapy. GCA occurred 4 months after the initiation of IO and responded promptly to the low-dose prednisone therapy. Four months after the continuation of nivolumab maintenance, the patient was hospitalized due to severe irAE encephalopathy which presented as psycho-behavioral abnormalities and progressive cognitive decline. He was treated with high-dose methylprednisolone which led to complete resolution of the symptoms and IO was permanently discontinued. The patient achieved a durable partial response. CONCLUSION: Both GCA and the subsequent encephalopathy in our patient responded well to the corticosteroid therapy, leading to the complete resolution of the symptoms and the patient achieved a durable partial response. Although the risk of severe neurologic irAEs affecting the central nervous system induced by IO re-administration, following previous discontinuation due to irAE, is not well-defined because of their rarity, this case highlights the need for caution, particularly in cases with a history of previous irAE-associated GCA.
Biomedical Center Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Bioptic Laboratory Ltd Pilsen Czech Republic
Sikl's Department of Pathology Faculty of Medicine Charles University Pilsen Czech Republic
Citace poskytuje Crossref.org
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