Toxic Epidermal Necrolysis Induced by Sintilimab: A Case Report.

Ya-Lei Lye, Bin Shan, Chen-Hong Jia, Jiang Liu, Juan Hou, Wen-Li Du, Rui Feng, Ping Liang
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Abstract

Sintilimab is an anti-programmed cell death receptor-1 antibody. The phase III clinical trial ORIENT-12 confirmed the safety of sintilimab combined with pemetrexed/platinum in the treatment of advanced squamous non-small cell lung cancer. Skin reactions are the most commonly reported adverse events of immune checkpoint inhibitors and are rarely severe. We describe a case of toxic epidermal necrolysis related to sintilimab in an elderly oncologic patient. 3 weeks after immunotherapy, the patient developed an extensive rash and diffuse itching, rapidly evolving into macules, blisters, bullae and erosions. Causal evaluation was performed based on the algorithm of drug causality for epidermal necrolysis and national Food and Drug Administration qualitative analysis. The patient responded to high-dose glucocorticosteroid and supportive therapy, alongside with local wound care. If immune checkpoint inhibitors need to be extrapolated clinically, strictly following evidence-based research, promptly detecting and treating adverse reactions is crucial.

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辛蒂利单抗诱导的毒性表皮坏死松解:一例报告。
辛蒂利单抗是一种抗程序性细胞死亡受体-1抗体。III期临床试验ORIENT-12证实了新替利单抗联合培美曲塞/铂治疗晚期鳞状非小细胞肺癌癌症的安全性。皮肤反应是免疫检查点抑制剂最常见的不良事件,很少严重。我们描述了一例与新替利单抗相关的老年肿瘤学患者的中毒性表皮坏死松解症。免疫治疗3周后,患者出现广泛皮疹和弥漫性瘙痒,迅速发展为黄斑、水疱、大疱和糜烂。基于表皮坏死松解药物因果关系算法和国家食品药品监督管理局定性分析进行因果评价。患者对高剂量糖皮质激素和支持性治疗以及局部伤口护理有反应。如果临床上需要推断免疫检查点抑制剂,严格遵循循证研究,及时发现和治疗不良反应至关重要。
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