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每日一次外用0.3%罗氟司特乳膏治疗帕博利珠单抗引起的瘙痒

The Treatment of Pembrolizumab-Induced Pruritus with Topical Roflumilast Cream 0.3% Once Daily.

作者信息

Lomax Laura

机构信息

Dr. Lomax is with Greensboro Dermatology Associates in Greensboro, North Carolina.

出版信息

J Clin Aesthet Dermatol. 2025 May 1;18(5):36-37.

Abstract

Pembrolizumab is an immune checkpoint inhibitor that is used in the treatment of various cancers. The reported mode of action of pembrolizumab is via binding to the PD-1 receptor which leads to blocking both immune-suppressing ligands, PD-L1 and PD-L2, from interacting with PD-1 to modulate the immune response. A common side effect of immune checkpoint inhibitors is pruritus, reported to occur in 14 to 47 percent of patients, which often reduces overall quality of life. This case report chronicles a patient suffering from significant pruritus and a lichenoid skin eruption after initiation of pembrolizumab treatment that was refractory to topical corticosteroid therapy, narrow band ultraviolet B light, and application of emollients. A topical phosphodiesterase-4 (PDE-4) inhibitor, roflumilast cream 0.3%, was subsequently initiated. Roflumilast is a selective inhibitor of PDE-4, approved by the United States Food and Drug Administration (FDA) in a 0.3% cream vehicle in 2022 for treatment of plaque psoriasis of any severity, and in a 0.3% foam vehicle in 2023 for treatment of seborrheic dermatitis of any severity. In 2024, roflumilast was FDA-approved in a 0.15% cream vehicle for treatment of mild-to-moderate atopic dermatitis in patients six years of age and older. In this adult patient, pruritus was improved within 48 hours after initiation of roflumilast cream 0.3% applied once daily and continued to be effective with use over time.

摘要

帕博利珠单抗是一种免疫检查点抑制剂,用于治疗多种癌症。据报道,帕博利珠单抗的作用方式是通过与PD-1受体结合,从而阻止免疫抑制配体PD-L1和PD-L2与PD-1相互作用,进而调节免疫反应。免疫检查点抑制剂的一种常见副作用是瘙痒,据报道,14%至47%的患者会出现这种情况,这通常会降低整体生活质量。本病例报告记录了一名患者在开始使用帕博利珠单抗治疗后出现严重瘙痒和苔藓样皮疹,局部使用皮质类固醇治疗、窄谱紫外线B光疗和涂抹润肤剂均无效。随后开始使用一种局部磷酸二酯酶-4(PDE-4)抑制剂,即0.3%的罗氟司特乳膏。罗氟司特是一种PDE-4选择性抑制剂,2022年美国食品药品监督管理局(FDA)批准其以0.3%乳膏剂型用于治疗任何严重程度的斑块状银屑病,2023年批准其以0.3%泡沫剂型用于治疗任何严重程度的脂溢性皮炎。2024年,罗氟司特以0.15%乳膏剂型获FDA批准,用于治疗6岁及以上患者的轻至中度特应性皮炎。在这名成年患者中,每天涂抹一次0.3%的罗氟司特乳膏后,瘙痒在48小时内得到改善,并且随着时间的推移持续有效。

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