Acute Infusion Pain Reaction Due to Anti-PD-1 Antibodies for the Treatment of Cutaneous Squamous Cell Carcinoma in Recessive Dystrophic Epidermolysis Bullosa: A Case Report and Review of the Literature.

Q3 Medicine
Case Reports in Dermatological Medicine Pub Date : 2025-02-26 eCollection Date: 2025-01-01 DOI:10.1155/crdm/4558623
Vanessa Tran, Susan J Robertson, Jamie Young, Malcolm Hogg, Alesha A Thai, Vanessa Morgan
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Abstract

Recessive dystrophic epidermolysis bullosa (RDEB) belongs to a rare group of inherited dermatoses, which are characterised by mucosal and cutaneous fragility. Cutaneous squamous cell carcinoma (CSCC) is a common complication of RDEB. In the severe subtype of RDEB (RDEB-S), CSCC is observed in 90% of the patients by 55 years. CSCC in patients with RDEB follows an aggressive course with the median survival rate of 2.4 years. We report the case of a 51-year-old female with RDEB with recurrent aggressive CSCC of the right lateral-back. She was commenced on cemiplimab, an anti-programmed death receptor-1 (PD-1) antibody, for the management of unresectable locally advanced CSCC; however, she experienced a severe infusion reaction, manifested as back pain, requiring treatment cessation. Despite three incomplete doses, the patient demonstrated a marked response with significant regression of her tumours. Therefore, further treatment was pursued. She was successfully administered cemiplimab under intravenous sedation. This was later complicated by immune-related colitis, necessitating treatment cessation. The patient was transitioned to best supportive care. The patient required inpatient admission for end-of-life care due to her complex analgesia requirements. This case report explores the pathophysiological mechanisms of pain in RDEB and anti-PD-1 antibody therapy and highlights the unique challenges of pain management in RDEB patients.

抗pd -1抗体治疗隐性营养不良大疱性表皮松解症皮肤鳞状细胞癌急性输注疼痛反应1例报告及文献复习
隐性营养不良大疱性表皮松解症(RDEB)属于一组罕见的遗传性皮肤病,其特征是粘膜和皮肤脆弱。皮肤鳞状细胞癌(CSCC)是RDEB的常见并发症。在RDEB的严重亚型(RDEB- s)中,90%的患者在55岁时观察到CSCC。RDEB患者的CSCC病程积极,中位生存率为2.4年。我们报告一例51岁女性RDEB伴复发性侵袭性CSCC右侧背。她开始使用抗程序性死亡受体-1 (PD-1)抗体cemiplimab治疗不可切除的局部晚期CSCC;然而,她经历了严重的输液反应,表现为背部疼痛,需要停止治疗。尽管三次剂量不完全,患者表现出明显的反应,肿瘤明显消退。因此,进行了进一步的治疗。她在静脉镇静下成功使用了西米单抗。这后来并发免疫相关性结肠炎,需要停止治疗。病人被转移到最好的支持性治疗。由于患者复杂的镇痛需求,该患者需要住院接受临终护理。本病例报告探讨了RDEB患者疼痛的病理生理机制和抗pd -1抗体治疗,并强调了RDEB患者疼痛管理的独特挑战。
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
CiteScore
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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