Mainville Laurence, Xu Lily, Piguet Vincent, Drucker Aaron M, Croitoru David O
Division of Dermatology, Department of Medicine, University of Toronto, Toronto, ON, Canada; Division of Dermatology, Department of Medicine, Women's College Hospital, Toronto, ON, Canada; Division of Dermatology, Department of Medicine, CHU de Québec-Université Laval, Québec, QC, Canada.
Toronto, Ontario, Canada.
Acta Derm Venereol. 2025 May 27;105:adv43667. doi: 10.2340/actadv.v105.43667.
Bullous pemphigoid (BP) is a chronic autoimmune blistering disease primarily affecting the elderly population. While awaiting the results from randomized clinical trials to assess the effect of dupilumab in patients with BP, clinicians have begun to introduce dupilumab into their therapeutic arsenal, with few data supporting their clinical decisions. The objectives were to assess time to disease control, predictors of response, achievement of disease control, disease recurrence, and occurrence of adverse events. Randomized and non-randomized studies of interventions (NRSIs) from Medline and Embase were reviewed. A total of 315 studies were identified and 5 NRSIs (167 participants with moderate-to-severe BP) meeting our inclusion criteria were found. Dupilumab was significantly associated with shorter time to disease control compared with the control group (HR 2.71 [95% CI, 1.85-3.96; I2 = 35%; 127 participants; 4 studies]). The overall strength of the evidence was graded as very low due to serious risk of bias and imprecision of effect measures. There were insufficient data to inform conclusions regarding BP recurrence and adverse events. Evidence was found that dupilumab reduces time to disease control in BP. It was not possible to assess predictors of response using pre-planned meta-regression. Randomized controlled trials are needed to determine dupilumab's place in therapeutic algorithms for BP. PROSPERO number: CRD42024599235.
大疱性类天疱疮(BP)是一种主要影响老年人群的慢性自身免疫性水疱病。在等待随机临床试验结果以评估度普利尤单抗对BP患者的疗效时,临床医生已开始将度普利尤单抗纳入其治疗手段,但支持其临床决策的数据很少。目的是评估疾病控制时间、反应预测因素、疾病控制的实现情况、疾病复发情况以及不良事件的发生情况。对来自Medline和Embase的干预措施随机和非随机研究(NRSIs)进行了综述。共识别出315项研究,发现5项NRSIs(共167例中重度BP患者)符合我们的纳入标准。与对照组相比,度普利尤单抗与更短的疾病控制时间显著相关(HR 2.71 [95% CI,1.85 - 3.96;I2 = 35%;127例参与者;4项研究])。由于存在严重的偏倚风险和效应测量的不精确性,证据的总体强度被评为非常低。没有足够的数据来得出关于BP复发和不良事件的结论。有证据表明度普利尤单抗可缩短BP的疾病控制时间。无法使用预先计划的meta回归来评估反应预测因素。需要进行随机对照试验来确定度普利尤单抗在BP治疗方案中的地位。PROSPERO编号:CRD42024599235。