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与程序性死亡-1(PD-1)受体抑制剂帕博利珠单抗相关的重症肌无力:一例40天病例报告

Myasthenia Gravis Associated With Programmed Death-1 (PD-1) Receptor Inhibitor Pembrolizumab: A 40-day Case Report.

作者信息

Ziobro Aidan S, LaPlante Reid L, DeMari Shayna R, Clark Larissa M, Kingsley David J, Smith Alyssa J

机构信息

UMDNJ, Newark, NJ, USA.

1091Albany College of Pharmacy and Health Sciences, Albany, NY, USA.

出版信息

J Pharm Pract. 2021 Feb;34(1):166-170. doi: 10.1177/0897190020970750. Epub 2020 Nov 4.

Abstract

PURPOSE

This case report describes myasthenia gravis-like symptoms after treatment with a programmed cell death 1 inhibitor, pembrolizumab, the treatment modalities utilized, and associated patient outcomes.

SUMMARY

A 76-year old male treated with pembrolizumab for palliative therapy for metastatic melanoma presented with increasing weakness, neck pain, diplopia in the left eye, abducens palsy, periorbital edema, and decreased appetite. The patient was diagnosed with acetylcholine receptor antibody (AChR) negative myasthenia gravis. The patient was started on prednisone 1 mg/kg/day, followed by pyridostigmine 60 mg by mouth 3 times a day, and IVIg for 5 days. Due to minor improvements in myasthenia gravis symptoms, 5 cycles of plasmapheresis were ordered. The patient was successfully treated for aspiration pneumonia after cardiopulmonary arrest. On day 28, the patient was diagnosed with ventilator associated pneumonia and received appropriate therapy. Due to ICU agitation and delirium, VAP, and long duration of treatment, the patient requested withdrawal of care and passed.

CONCLUSION

Programmed cell death inhibitors, such as pembrolizumab, can provide great benefit to patients but can also be associated with rare but serious adverse events. With new reports of MG after use, providers should continually weigh the benefits versus harm in using these products and monitor patients closely for such adverse events.

摘要

目的

本病例报告描述了程序性细胞死亡蛋白1抑制剂帕博利珠单抗治疗后出现的重症肌无力样症状、所采用的治疗方式以及相关的患者预后情况。

摘要

一名76岁男性因转移性黑色素瘤接受帕博利珠单抗姑息治疗,出现肌无力加重、颈部疼痛、左眼复视、展神经麻痹、眶周水肿和食欲减退。该患者被诊断为乙酰胆碱受体抗体(AChR)阴性重症肌无力。患者开始服用泼尼松1mg/kg/天,随后口服吡啶斯的明60mg,每日3次,并静脉注射免疫球蛋白5天。由于重症肌无力症状有轻微改善,安排了5个疗程的血浆置换。患者在心肺骤停后成功治疗了吸入性肺炎。在第28天,患者被诊断为呼吸机相关性肺炎并接受了适当治疗。由于重症监护病房的躁动和谵妄、呼吸机相关性肺炎以及治疗时间长,患者要求停止治疗并最终去世。

结论

程序性细胞死亡抑制剂,如帕博利珠单抗,可为患者带来巨大益处,但也可能与罕见但严重的不良事件相关。随着使用后出现重症肌无力的新报告,医疗服务提供者应持续权衡使用这些产品的利弊,并密切监测患者是否出现此类不良事件。

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