Autoimmune encephalitis following treatment with durvalumab for small-cell lung cancer.

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Journal of International Medical Research Pub Date : 2024-10-01 DOI:10.1177/03000605241287015
Yu-Lan Qian, Ye Jiang, Yin-Hua Gong, Jian-Kang Yu, Chao Liu, Wen-Ting Wu, Dan Shen
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Abstract

The traditional treatment for small-cell lung cancer (SCLC) has been traditional systemic platinum-containing chemotherapy because the response rate is 50-90%. Durvalumab is an immune checkpoint inhibitor that blocks the binding of programmed cell death protein 1 and programmed cell death 1 ligand 1. Durvalumab combined with traditional chemotherapy agents has been recommended as the first-line treatment for extensive-stage SCLC, but its use may cause immune-related adverse events. Autoimmune encephalitis is a rare and potentially fatal neurological adverse event. This current case report describes a male patient in his late 50s with ES-SCLC who developed autoimmune encephalitis associated with durvalumab treatment after three cycles of combination chemotherapy. This current case furthers the understanding of autoimmune encephalitis caused by durvalumab treatment.

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使用durvalumab治疗小细胞肺癌后出现自身免疫性脑炎。
小细胞肺癌(SCLC)的传统治疗方法是传统的全身性含铂化疗,因为其反应率为50%-90%。Durvalumab是一种免疫检查点抑制剂,可阻断程序性细胞死亡蛋白1和程序性细胞死亡配体1的结合。Durvalumab与传统化疗药物联合使用,已被推荐为广泛期SCLC的一线治疗方法,但其使用可能导致免疫相关不良事件。自身免疫性脑炎是一种罕见且可能致命的神经系统不良事件。本病例报告描述了一名 50 多岁的 ES-SCLC 男性患者在接受三个周期的联合化疗后,出现了与 durvalumab 治疗相关的自身免疫性脑炎。本病例加深了人们对杜伐单抗治疗引起的自身免疫性脑炎的认识。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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