Tskhvarashvili G, Aher K, Sveide I, Katus U, Westerlund A, Hoti F, Wennerström C, Hassan F, Lee J, Hermanrud C, Johnsson I, Passey A, Nissinen R, Polesie S, Mälkönen T, Saarelainen L
Epidemiology and Database Studies, IQVIA, Tallinn, Estonia.
Biostatistics, IQVIA, Tallinn, Estonia.
J Eur Acad Dermatol Venereol. 2025 Mar;39 Suppl 1(Suppl 1):50-64. doi: 10.1111/jdv.20198. Epub 2024 Aug 2.
Plaque psoriasis (PsO) requires long-term treatment for symptom control and remission; thus, a long-term pharmacological intervention is necessary. Treatment persistence reflects long-term therapeutic effectiveness and tolerance.
This study investigates drug persistence and compares treatment discontinuation rates across biologic agents and apremilast used by PsO patients in Finland and Sweden.
This retrospective register-based cohort study included bio-naïve patients (≥18 years) with moderate-to-severe PsO, who initiated treatment with abatacept, adalimumab, brodalumab, certolizumab pegol, etanercept, golimumab, guselkumab, ixekizumab, risankizumab, secukinumab, tildrakizumab, ustekinumab or apremilast during 2008-2020 in Finland or Sweden. The main analysis evaluated persistence (based on duration of continuous treatment) and compared rates of treatment discontinuation using guselkumab as reference drug, during 2018-2020 in Finland. Treatment discontinuation was assessed by survival analysis of the time to first drug discontinuation, including switching to other study drugs. Due to limited sample size (n < 20), certain biologics (abatacept, brodalumab, certolizumab pegol, etanercept, golimumab, risankizumab and tildrakizumab) were excluded from the persistence analysis.
In Finland, 709 patients fulfilled the inclusion criteria during 2018-2020 for the main analysis. The highest persistence was observed for guselkumab and ustekinumab with 90 and 85% of treated patients, respectively, continuing treatment for ≥1 year. Comparable results were observed in the expanded cohort analysis (index starting in 2008; 2745 bio-naïve patients in Finland and 10,970 in Sweden). Furthermore, patients treated with guselkumab in Finland showed lower treatment discontinuation rates compared to other study drugs.
Guselkumab and ustekinumab demonstrated high persistence as measured by continued treatment for at least 1 year. Furthermore, these treatments demonstrated lower rates of discontinuation compared to other study drugs included in the analysis. Understanding the balance between efficacy and feasibility in treatment decisions is crucial, as feasibility may impact persistency outcomes and potentially increase persistency rates.
斑块状银屑病(PsO)需要长期治疗以控制症状和实现缓解;因此,长期的药物干预是必要的。治疗持续性反映了长期治疗效果和耐受性。
本研究调查药物持续性,并比较芬兰和瑞典PsO患者使用的生物制剂和阿普米拉斯的治疗停药率。
这项基于登记的回顾性队列研究纳入了初治(≥18岁)的中重度PsO患者,他们于2008年至2020年期间在芬兰或瑞典开始使用阿巴西普、阿达木单抗、布罗达单抗、赛妥珠单抗、依那西普、戈利木单抗、古塞库单抗、司库奇尤单抗、瑞莎珠单抗、苏金单抗、替拉珠单抗、乌司奴单抗或阿普米拉斯进行治疗。主要分析评估持续性(基于连续治疗时间),并以古塞库单抗作为对照药物,比较2018年至2020年期间芬兰的治疗停药率。通过首次停药时间的生存分析评估治疗停药情况,包括换用其他研究药物。由于样本量有限(n < 20),某些生物制剂(阿巴西普、布罗达单抗、赛妥珠单抗、依那西普、戈利木单抗、瑞莎珠单抗和替拉珠单抗)被排除在持续性分析之外。
在芬兰进行主要分析期间,2018年至2020年有709例患者符合纳入标准。观察到古塞库单抗和乌司奴单抗的持续性最高,分别有90%和85%接受治疗的患者持续治疗≥1年。在扩展队列分析(起始于2008年;芬兰2745例初治患者,瑞典10970例)中观察到了类似结果。此外,在芬兰接受古塞库单抗治疗的患者与其他研究药物相比,治疗停药率较低。
按照至少持续治疗1年衡量,古塞库单抗和乌司奴单抗显示出高持续性。此外,与分析中纳入的其他研究药物相比,这些治疗的停药率较低。在治疗决策中理解疗效和可行性之间的平衡至关重要,因为可行性可能影响持续性结果并有可能提高持续性率。