Postimmunotherapy antiglial fibrillary acidic protein encephalomyelitis after adjuvant pembrolizumab for melanoma.

IF 1.5 4区 医学 Q3 DERMATOLOGY
Inès Berkaoui, Linda Zourdani, Raphaël Janela-Lapert
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引用次数: 0

Abstract

Pembrolizumab is an immune checkpoint inhibitor targeting programmed cell death protein 1 , used for stage IIB/IIC melanoma. While effective, pembrolizumab can lead to immune-mediated toxicities in various systems; however, nervous system effects are less well-documented. We report the case of a 34-year-old man who developed delayed immune-mediated encephalomyelitis with antiglial fibrillary acidic protein (GFAP) antibodies after completing nine cycles of adjuvant pembrolizumab for stage IIC melanoma. Four months posttreatment, he presented with neurological symptoms, including ataxic gait, sensory deficits in the lower limbs, and urinary retention. Imaging revealed extensive myelitis and encephalitis in the spinal cord and posterior fossa. The etiological evaluation was negative except for the presence of anti-GFAP antibodies in the cerebrospinal fluid. Treatment with high-dose corticosteroids led to significant improvement. This case represents the first reported instance of postimmunotherapy encephalomyelitis with anti-GFAP antibodies following pembrolizumab treatment. Although rare, this is a serious adverse event requiring careful monitoring and early multidisciplinary management.

pembrolizumab辅助治疗黑色素瘤后抗神经胶质纤维酸性蛋白脑脊髓炎。
Pembrolizumab是一种针对程序性细胞死亡蛋白1的免疫检查点抑制剂,用于IIB/IIC期黑色素瘤。虽然有效,但派姆单抗可导致各种系统的免疫介导毒性;然而,神经系统的影响却没有得到充分的证明。我们报告了一例34岁的男性患者,在完成9个周期的辅助派姆单抗治疗IIC期黑色素瘤后,出现了伴抗胶质纤维酸性蛋白(GFAP)抗体的延迟性免疫介导性脑脊髓炎。治疗4个月后,患者出现神经系统症状,包括步态共济失调、下肢感觉缺陷和尿潴留。影像学显示脊髓和后窝有广泛的脊髓炎和脑炎。除了脑脊液中存在抗gfap抗体外,病因学评估为阴性。大剂量皮质类固醇治疗可显著改善。该病例是经派姆单抗治疗后出现抗gfap抗体的刺激治疗后脑脊髓炎的首例报道。虽然罕见,但这是一个严重的不良事件,需要仔细监测和早期多学科管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Melanoma Research
Melanoma Research 医学-皮肤病学
CiteScore
3.40
自引率
4.50%
发文量
139
审稿时长
6-12 weeks
期刊介绍: ​​​​​​Melanoma Research is a well established international forum for the dissemination of new findings relating to melanoma. The aim of the Journal is to promote the level of informational exchange between those engaged in the field. Melanoma Research aims to encourage an informed and balanced view of experimental and clinical research and extend and stimulate communication and exchange of knowledge between investigators with differing areas of expertise. This will foster the development of translational research. The reporting of new clinical results and the effect and toxicity of new therapeutic agents and immunotherapy will be given emphasis by rapid publication of Short Communications. ​Thus, Melanoma Research seeks to present a coherent and up-to-date account of all aspects of investigations pertinent to melanoma. Consequently the scope of the Journal is broad, embracing the entire range of studies from fundamental and applied research in such subject areas as genetics, molecular biology, biochemistry, cell biology, photobiology, pathology, immunology, and advances in clinical oncology influencing the prevention, diagnosis and treatment of melanoma.
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