Department of Allergy & Immunology, Huashan Hospital affiliated to Fudan University, Shanghai, China.
Department of Dermatology, Huashan Hospital affiliated to Fudan University, Shanghai, China.
Dermatol Ther. 2022 Aug;35(8):e15648. doi: 10.1111/dth.15648. Epub 2022 Jul 1.
Routine systemic therapy for bullous pemphigoid (BP) has been challenged due to the inevitably adverse effects. According to the successful applications of dupilumab in BP cases reported, therefore, we investigate the real-life efficacy and safety of dupilumab combined with low-dose oral steroid for BP. A cohort of BP patients who received either dupilumab plus low-dose methylprednisolone (dupilumab group) or merely methylprednisolone (control group) was retrospectively reviewed. The time to disease control was investigated. Additionally, the control dose and cumulative dosage of steroids, Bullous Pemphigoid Disease Area Index (BPDAI) scores, pruritus scores, and adverse events were assessed. A total of 40 patients, with 20 in each group, were retrospectively studied. The time to disease control was shorter in the dupilumab group than the control group (14 days vs. 19 days, p = 0.043). When the disease was controlled, the control dose and cumulative dosage of methylprednisolone in the dupilumab group were substantially lower than those of the control (24.6 mg vs. 48.8 mg, 376.8 mg vs. 985.6 mg, both p < 0.01). Compared with the control, the percentage change from baseline in BPDAI scores and pruritus scores were both significantly reduced, and the adverse events were also less frequent in the dupilumab group. The combination therapy of dupilumab plus low-dose methylprednisolone exhibits superior efficacy and safety in comparison with the current first-line systemic therapy for BP.
由于不可避免的不良反应,常规的全身性治疗对大疱性类天疱疮(BP)的疗效受到了挑战。根据已报道的成功应用度普利尤单抗治疗 BP 的案例,我们研究了度普利尤单抗联合低剂量口服类固醇治疗 BP 的真实疗效和安全性。我们回顾性分析了接受度普利尤单抗联合低剂量甲泼尼龙(度普利尤单抗组)或单纯甲泼尼龙(对照组)治疗的 BP 患者队列。研究了疾病控制的时间。此外,还评估了类固醇的控制剂量和累积剂量、大疱性类天疱疮疾病面积指数(BPDAI)评分、瘙痒评分和不良反应。共回顾性研究了 40 例患者,每组 20 例。度普利尤单抗组的疾病控制时间短于对照组(14 天 vs. 19 天,p=0.043)。当疾病得到控制时,度普利尤单抗组的类固醇控制剂量和累积剂量明显低于对照组(24.6mg 与 48.8mg,376.8mg 与 985.6mg,均 p<0.01)。与对照组相比,度普利尤单抗组的 BPDAI 评分和瘙痒评分的基线百分比变化均显著降低,且不良反应也较少。与目前 BP 的一线全身性治疗相比,度普利尤单抗联合低剂量甲泼尼龙的联合治疗具有更好的疗效和安全性。