一名获得持久部分应答的转移性肾细胞癌患者因免疫疗法引发巨细胞颞动脉炎和严重脑病:病例报告。

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2024-08-26 eCollection Date: 2024-01-01 DOI:10.1159/000540660
Ondřej Fiala, Michaela Tkadlecová, Kristýna Pivovarčíková, Jan Baxa, Petr Stránský, Dominika Šiková, Milan Hora, Jindřich Fínek
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引用次数: 0

摘要

简介:联合免疫肿瘤学(IO)疗法是目前转移性肾细胞癌(mRCC)一线系统疗法的基石。尽管联合 IO 方案显示出很高的疗效,但它们往往伴随着各种免疫相关不良反应(irAEs):我们描述了一例罕见的免疫相关不良反应(irAEs),表现为巨细胞颞动脉炎(GCA),随后在继续接受免疫治疗后出现严重脑病,患者是一名66岁的男性mRCC患者,在一线系统治疗中接受了ipilimumab和nivolumab的联合治疗。GCA发生在开始IO治疗4个月后,并对小剂量泼尼松治疗迅速做出反应。在继续使用 nivolumab 维持治疗 4 个月后,患者因严重的 irAE 脑病住院,表现为精神行为异常和进行性认知能力下降。他接受了大剂量甲基强的松龙治疗,症状完全缓解,IO也被永久停用。患者获得了持久的部分应答:结论:本例患者的 GCA 和随后出现的脑病对皮质类固醇治疗反应良好,导致症状完全缓解,患者获得了持久的部分应答。尽管因虹膜睫状体异常而停用 IO 后,再次给药会诱发影响中枢神经系统的严重神经系统虹膜睫状体异常的风险因其罕见而尚未明确,但本病例强调了谨慎的必要性,尤其是在既往有虹膜睫状体异常相关 GCA 病史的病例中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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