环孢素治疗奥麦珠单抗难治性慢性荨麻疹5例报告。

Anthony F LaCava, Olajumoke O Fadugba
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摘要

背景:虽然AAAAI/ACAAI和EAACI/GA2LEN/EuroGuiDerm/APAAACI指南都推荐对奥玛珠单抗反应不足的慢性荨麻疹患者开始使用环孢素,但由于缺乏临床数据,许多临床医生对开始使用环孢素犹豫不决。本研究的目的是报告对奥玛珠单抗反应不足并从奥玛珠单抗切换到环孢素的慢性荨麻疹成年患者的现实临床结果。我们回顾性地回顾了成年慢性荨麻疹患者的医疗记录,这些患者对奥玛珠单抗反应不足,后来用环孢素治疗。记录有关治疗方法、临床反应和不良反应的数据。结果/病例表现:5例奥玛珠单抗难治性慢性荨麻疹患者,其中3例伴有血管性水肿,1例伴有诱导性荨麻疹,采用低剂量口服环孢素(1-3 mg/kg/d)治疗。在本病例系列中,五分之四的患者在继续其他标准治疗的同时,口服环孢素完全缓解了症状。3例患者出现全身副作用,2例患者停药。讨论:单独使用环孢素可以有效地诱导对奥玛珠单抗反应不足的成人慢性荨麻疹患者的荨麻疹控制,尽管环孢素的影响受到可逆不良反应的限制。不良反应与先前存在的医疗状况有关。随着新的慢性荨麻疹治疗方法的研究,这一经验强调了揭示慢性荨麻疹亚型的重要性,这些亚型往往对环孢素有反应,同时提供耐受性更好的替代治疗。
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Cyclosporine for omalizumab-refractory chronic urticaria: a report of five cases.

Background: While both the AAAAI/ACAAI and the EAACI/GA2LEN/EuroGuiDerm/APAAACI guidelines recommend starting cyclosporine for patients with chronic urticaria who have had an inadequate response to omalizumab, many clinicians are hesitant to initiate cyclosporine due to paucity of clinical data. The objective of this study was to report real-life clinical outcomes in adult patients with chronic urticaria who had an inadequate response to omalizumab and were switched from omalizumab to cyclosporine. Medical records of adult patients with chronic urticaria who had an inadequate response with omalizumab and were later treated with cyclosporine were reviewed retrospectively. Data pertaining to treatment method, clinical response, and adverse effects were recorded.

Results/presentation of cases: Five patients with omalizumab-refractory chronic urticaria, three of whom also had angioedema and one with an inducible urticaria, were treated with low doses of oral cyclosporine (1-3 mg/kg/d). Four of five patients in this case series had complete resolution of symptoms with oral cyclosporine, while continuing other standard therapies. Systemic side effects occurred in three patients which prompted drug discontinuation in two patients.

Discussion: Cyclosporine alone was effective in inducing urticaria control in adult patients with chronic urticaria who had an inadequate response to omalizumab, though the impact of cyclosporine was limited by reversible adverse effects. Adverse effects were associated with pre-existing medical conditions. As novel chronic urticaria therapies are being investigated, this experience highlights the importance of uncovering chronic urticaria subtypes which tend to respond to cyclosporine, while providing alternative treatments with better tolerability.

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