de Bruin-Weller Marjolein S, Serra-Baldrich Esther, Barbarot Sebastien, Grond Susanne, Schuster Christopher, Petto Helmut, Capron Jean-Philippe, Raibouaa Afaf, Werfel Thomas
Department of Dermatology and Allergology, University Medical Center, Utrecht, The Netherlands.
Department of Dermatology, Cutaneous Allergy Unit, Hospital Sant Pau, Universitat Autònoma Barcelona, Barcelona, Spain.
Dermatol Ther (Heidelb). 2022 Jun;12(6):1481-1491. doi: 10.1007/s13555-022-00734-w. Epub 2022 May 11.
Indirect treatment comparison was used to compare approved doses of baricitinib and dupilumab for treating adult patients with moderate-to-severe atopic dermatitis (AD) who are candidates for systemic therapy.
Baricitinib and dupilumab were compared (Bucher method) at weeks 4 and 16. Performance in combination with topical corticosteroids (TCS) was analyzed in patients with inadequate response or inadvisable to topical therapies (population A) and cyclosporine (population B). Population A was additionally examined as monotherapy.
For the Eczema Area and Severity Index (EASI) 75, baricitinib and dupilumab were similar. A ≥ 4-point improvement in itch numerical rating scale (NRS) was significantly more likely with baricitinib 4 mg than dupilumab in population A as monotherapy (RR = 2.62, 95% CI 1.22, 5.61, p = 0.013) and in TCS combination at week 4. These differences were not significant by week 16. For the Dermatology Life Quality Index (DLQI), baricitinib 4 mg and dupilumab were similar on mean difference in change from baseline (MDcfb), though some differences were seen between baricitinib 2 mg and dupilumab at week 16 for the population A monotherapy (MDcfb = 2.05, 95% CI 0.53, 3.56, p = 0.016) and TCS combination therapy (MDcfb = 2.48, 95% CI 0.46, 4.50, p = 0.016) groups, and in population B (MDcfb = 3.38 95% CI 1.18, 5.58, p = 0.003).
Baricitinib potentially offers more rapid improvement in itch while providing similar efficacy on EASI75 and DLQI outcomes compared with dupilumab.
采用间接治疗比较方法,比较巴瑞替尼和度普利尤单抗的获批剂量,用于治疗适合进行系统治疗的中度至重度特应性皮炎(AD)成年患者。
在第4周和第16周比较巴瑞替尼和度普利尤单抗(布彻方法)。对局部皮质类固醇(TCS)反应不足或不宜采用局部治疗的患者(A组)以及环孢素治疗患者(B组),分析其与TCS联合使用时的疗效。A组还作为单一疗法进行了检查。
对于湿疹面积和严重程度指数(EASI)改善75%的情况,巴瑞替尼和度普利尤单抗相似。在A组作为单一疗法时(风险比[RR]=2.62,95%置信区间[CI]1.22,5.61,p=0.013)以及在第4周与TCS联合使用时,巴瑞替尼4mg组瘙痒数字评定量表(NRS)改善≥4分的可能性显著高于度普利尤单抗组。到第16周时,这些差异不再显著。对于皮肤病生活质量指数(DLQI),巴瑞替尼4mg组和度普利尤单抗组从基线变化的平均差异(MDcfb)相似,不过在第16周时,A组单一疗法(MDcfb=2.05,95%CI 0.53,3.56,p=0.016)和TCS联合治疗组(MDcfb=2.48,95%CI 0.46,4.50,p=0.016)以及B组(MDcfb=3.38,95%CI 1.18,5.58,p=0.003)中,巴瑞替尼2mg组和度普利尤单抗组之间存在一些差异。
与度普利尤单抗相比,巴瑞替尼可能在瘙痒改善方面起效更快,同时在EASI75和DLQI结果上提供相似的疗效。