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伊匹木单抗诱发转移性黑色素瘤患者重症肌无力

Myasthenia Gravis Induced by Ipilimumab in a Patient With Metastatic Melanoma.

作者信息

Montes Vera, Sousa Sandra, Pita Fernando, Guerreiro Rui, Carmona Cátia

机构信息

Department of Neurology, Cascais Hospital Dr. José de Almeida, Lisboa, Portugal.

出版信息

Front Neurol. 2018 Apr 3;9:150. doi: 10.3389/fneur.2018.00150. eCollection 2018.

Abstract

In daily clinical practice, there is a growing number of patients receiving new biological agents used in the treatment of malignancies. Ipilimumab is a fully humanized monoclonal antibody approved for patients with melanoma. It acts as an immune checkpoint inhibitor, binding and blocking cytotoxic T-lymphocyte antigen-4 in order to increase the antitumor immune response. There are several reports of autoimmune responses after its use. A 74-year-old man developed a mild rash and pruritus a few hours after the second infusion of ipilimumab and 24 h after the third dose of ipilimumab, he presented with shortness of breath, proximal limb muscle weakness, and diplopia. Repetitive nerve stimulation was consistent with a postsynaptic neuromuscular junction disorder. He began therapy with corticosteroids and pyridostigmine and ipilimumab was discontinued. Following ipilimumab suspension, the patient started to improve gradually. Here, we describe a rare case of myasthenia gravis presumably related with ipilimumab's therapy. A better knowledge of these agents is necessary, in order to identify characteristics or biomarkers that may be associated with the development of potentially serious autoimmune responses.

摘要

在日常临床实践中,接受用于治疗恶性肿瘤的新型生物制剂的患者数量日益增多。伊匹单抗是一种已获批用于黑色素瘤患者的全人源单克隆抗体。它作为一种免疫检查点抑制剂,通过结合并阻断细胞毒性T淋巴细胞抗原4,以增强抗肿瘤免疫反应。使用该药物后有几例关于自身免疫反应的报道。一名74岁男性在第二次输注伊匹单抗后数小时出现轻度皮疹和瘙痒,在第三次注射伊匹单抗24小时后,出现呼吸急促、近端肢体肌肉无力和复视。重复神经电刺激结果符合突触后神经肌肉接头疾病。他开始接受皮质类固醇和吡啶斯的明治疗,伊匹单抗停药。停用伊匹单抗后,患者逐渐好转。在此,我们描述了一例可能与伊匹单抗治疗相关的罕见重症肌无力病例。为了识别可能与潜在严重自身免疫反应发生相关的特征或生物标志物,有必要更好地了解这些药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b0e/5891586/edad3ffbb56b/fneur-09-00150-g001.jpg

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