Alabas Oras A, Mason Kayleigh J, Yiu Zenas Z N, Hampton Philip J, Reynolds Nick J, Owen Caroline M, Bewley Anthony, Laws Philip M, Warren Richard B, Lunt Mark, Smith Catherine H, Griffiths Christopher E M
Centre for Dermatology Research, University of Manchester, NIHR Manchester Biomedical Research Centre, Manchester, UK.
Primary Care Centre Versus Arthritis, School of Medicine, Keele University, Keele, UK.
Br J Dermatol. 2023 Apr 20;188(5):618-627. doi: 10.1093/bjd/ljad004.
Real-world data evaluating effectiveness and persistence of systemic therapies for patients with psoriasis are limited. Objectives To determine the effectiveness and persistence of acitretin, ciclosporin, fumaric acid esters (FAEs) and methotrexate in patients with moderate-to-severe psoriasis.
Data from the British Association of Dermatologists Biologics and Immunomodulators Register (BADBIR), a prospective, multicentre pharmacovigilance register of patients with moderate-to-severe psoriasis receiving biologic and/or conventional systemic therapies, were analysed. Eligible patients were ≥ 16 years of age receiving a first course of acitretin, ciclosporin, FAEs or methotrexate between 2007 and 2021 with ≥ 6 months' follow-up. Effectiveness was defined as achieving absolute Psoriasis Area and Severity Index (aPASI) ≤ 2 reported ≥ 4 weeks after treatment start date until date of cessation. To identify baseline clinical variables associated with treatment effectiveness, we used multivariable logistic regression models estimating the adjusted odds ratio (aOR) of achieving aPASI ≤ 2. To describe drug persistence associated with ineffectiveness, occurrence of adverse events or other reasons for discontinuation, survival estimates with 95% confidence intervals (CIs) were obtained using a flexible parametric model. Results were obtained using multiple imputed data.
In total, 5430 patients were included in the analysis. Overall, 1023 (19%) patients were receiving acitretin, 1401 (26%) patients were on ciclosporin, 347 (6%) patients were on FAEs, and 2659 (49%) patients were receiving methotrexate at registration. The proportion of patients who achieved aPASI ≤ 2 was lower for those treated with acitretin [n = 118 (21%)] compared with those receiving ciclosporin [n = 233 (34%)], FAEs [n = 43 (29%)] and methotrexate [n = 372 (32%)]. Factors associated with ineffectiveness included prior experience to previous nonbiologic systemic therapies (acitretin) (aOR 0.64, 95% CI 0.42-0.96), male sex (methotrexate) (aOR 0.58, 95% CI 0.46-0.74), comorbidities (aOR 0.70, 95% CI 0.51-0.97) and alcohol consumption (≤ 14 units per week) (ciclosporin) (aOR 0.70, 95% CI 0.50-0.98). Persistence associated with all reasons for discontinuation showed better survival for methotrexate compared with acitretin, ciclosporin and FAEs cohorts at 12 months [survival estimate 46.1 (95% CI 44.0-48.3), 31.9 (95% CI 29.4-34.7), 30.0 (95% CI 27.5-32.4) and 35.0 (95% CI 29.9-40.9), respectively].
The real-world effectiveness and persistence of acitretin, ciclosporin, FAEs and methotrexate were generally low. Previous nonbiologic systemic therapies, male sex, comorbidities and alcohol consumption were risk factors associated with treatment ineffectiveness.
评估银屑病患者系统治疗有效性和持久性的真实世界数据有限。目的:确定阿维A、环孢素、富马酸酯(FAEs)和甲氨蝶呤治疗中重度银屑病患者的有效性和持久性。
分析英国皮肤科医师协会生物制剂和免疫调节剂登记处(BADBIR)的数据,这是一个前瞻性、多中心的药物警戒登记处,登记了接受生物和/或传统系统治疗的中重度银屑病患者。符合条件的患者年龄≥16岁,在2007年至2021年间接受阿维A、环孢素、FAEs或甲氨蝶呤的首个疗程治疗,随访时间≥6个月。有效性定义为在治疗开始日期至停药日期后≥4周报告达到绝对银屑病面积和严重程度指数(aPASI)≤2。为了确定与治疗有效性相关的基线临床变量,我们使用多变量逻辑回归模型估计达到aPASI≤2的调整优势比(aOR)。为了描述与无效、不良事件发生或其他停药原因相关的药物持久性,使用灵活的参数模型获得95%置信区间(CIs)的生存估计值。结果使用多重插补数据获得。
总共5430名患者纳入分析。总体而言,登记时1023名(19%)患者接受阿维A治疗,1401名(26%)患者接受环孢素治疗,347名(6%)患者接受FAEs治疗,2659名(49%)患者接受甲氨蝶呤治疗。与接受环孢素[n = 233(34%)]、FAEs[n = 43(29%)]和甲氨蝶呤[n = 372(32%)]治疗的患者相比,接受阿维A治疗的患者达到aPASI≤2的比例较低[n = 118(21%)]。与无效相关的因素包括既往非生物系统治疗(阿维A)的经验(aOR 0.64,95% CI 0.42 - 0.96)、男性(甲氨蝶呤)(aOR 0.58,95% CI 0.46 - 0.74)、合并症(aOR 0.70,95% CI 0.51 - 0.97)和饮酒量(每周≤14单位)(环孢素)(aOR 0.70,95% CI 0.50 - 0.98)。与所有停药原因相关的持久性显示,在12个月时,甲氨蝶呤组的生存率高于阿维A、环孢素和FAEs组[生存估计值分别为46.1(95% CI 44.0 - 48.3)、31.9(95% CI 29.4 - 34.7)、30.0(95% CI 27.5 - 32.4)和35.0(95% CI 29.9 - 40.9)]。
阿维A、环孢素、FAEs和甲氨蝶呤的真实世界有效性和持久性普遍较低。既往非生物系统治疗、男性、合并症和饮酒是与治疗无效相关的危险因素。