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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

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Author
Fiala, OndřejORCiD Profile - 0000-0002-4096-7385Scopus Profile - 36627065100
Tkadlecová, Michaela
Pivovarčíková, KristýnaORCiD Profile - 0000-0002-9553-0105WoS Profile - Q-5634-2018Scopus Profile - 56003922800
Baxa, JanORCiD Profile - 0000-0002-4896-1658WoS Profile - J-5777-2015Scopus Profile - 35613051400
Stránský, Petr
Šiková, Dominika
Hora, MilanORCiD Profile - 0000-0002-5061-3687Scopus Profile - 7004855950
Fínek, JindřichORCiD Profile - 0000-0002-7750-9345Scopus Profile - 55941838000

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Publication date
2024
Published in
Case Reports in Oncology
Volume / Issue
17 (1)
ISBN / ISSN
ISSN: 1662-6575
ISBN / ISSN
eISSN: 1662-6575
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  • Faculty of Medicine in Pilsen

This publication has a published version with DOI 10.1159/000540660

Abstract
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.
Keywords
Encephalopathy, Giant cell arteritis, Immune-related adverse effects, Immune-related adverse events, Immunotherapy, Nivolumab, Renal cell carcinoma
Permanent link
https://hdl.handle.net/20.500.14178/2640
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WOS:001316217400001
SCOPUS:2-s2.0-85203055920
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