首页> 外文期刊>Journal of the European Academy of Dermatology and Venereology: JEADV >Secukinumab treatment leads to normalization of quality of life and disease symptoms in psoriasis patients with or without prior systemic psoriasis therapy: the PROSE study results
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Secukinumab treatment leads to normalization of quality of life and disease symptoms in psoriasis patients with or without prior systemic psoriasis therapy: the PROSE study results

机译:Secukinumab治疗导致牛皮癣患者的生命和疾病症状质量的正常化:散文研究结果

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Introduction Psoriatic disease is associated with considerable impairment of quality of life (QoL). The PROSE study (NCT02752776) investigated the impact of secukinumab treatment on patient-reported outcomes (PRO) in patients with moderate to severe psoriasis stratified by their treatment history. Methods PROSE was a prospective, non-randomised, multicentre study. Patients were categorized at baseline according to treatment history as naive [naive to any systemic therapy (N = 663)], conventional systemic [previously exposed to >= 1 conventional systemic (CS) therapy (N = 673)] and biologics [previously exposed to >= 1 biologic therapy (N = 324)]. QoL PROs, efficacy and safety of secukinumab 300 mg were assessed for a period of 52 weeks. Results The primary objective was met with 70.8% patients achieving a Dermatology Life Quality Index (DLQI) 0/1 response at Week 16 (na & x3ca;ve, 74.7%; CS, 71.3%; biologic, 61.7%), with effects sustained up to Week 52. Mean Family DLQI (FDLQI) score decreased from 11.5 at baseline (na & x3ca;ve, 11.3; CS, 11.4; biologic, 12.1) to 2.5 at Week 16 (na & x3ca;ve, 2.5; CS, 2.3; biologic: 3.5). Substantial improvements in EuroQoL 5-Dimension Health Questionnaire, Numeric Rating Scale for pain, itching and scaling, Health Assessment Questionnaire-Disability Index, Treatment Satisfaction Questionnaire for Medication, and Patient Benefit Index were also observed at Week 16. The QoL gains were associated with substantial improvements in Psoriasis Area and Severity Index and Investigator Global Assessment mod 2011 0/1 response. No meaningful difference was observed in the efficacy or QoL improvements across patient subpopulations. All QoL and efficacy parameter improvements were sustained up to Week 52. Secukinumab treatment was well-tolerated, and no new safety signals were observed. Conclusion Secukinumab treatment resulted in complete normalization of QoL in a substantial proportion of psoriasis patients, and their families, regardless of their prior treatment history.
机译:简介银屑病与生活质量(QoL)的严重损害有关。PROSS研究(NCT02752776)调查了塞库单抗治疗对中重度银屑病患者的患者报告结果(PRO)的影响,根据患者的治疗史进行分层。方法采用前瞻性、非随机、多中心研究。根据治疗史,患者在基线检查时被分为未接受任何系统治疗(N=663)、常规系统治疗(N=673)和生物制剂(N=324)。在52周的时间内评估300 mg塞库单抗的生活质量优势、疗效和安全性。结果70.8%的患者在第16周达到皮肤病生活质量指数(DLQI)0/1的反应(na&x3ca;ve,74.7%;CS,71.3%;Biological,61.7%)达到了主要目标,效果持续到第52周。平均家庭DLQI(FDLQI)评分从基线检查时的11.5分(na&x3ca;ve,11.3;CS,11.4;生物学,12.1)降至第16周时的2.5分(na&x3ca;ve,2.5;CS,2.3;生物学:3.5)。在第16周,还观察到EuroQoL 5维健康问卷、疼痛、瘙痒和脱屑数字评分量表、健康评估问卷残疾指数、药物治疗满意度问卷和患者受益指数的显著改善。生活质量的提高与银屑病面积和严重程度指数的显著改善以及研究者2011年mod全球评估0/1反应有关。不同患者亚群的疗效或生活质量改善无显著差异。所有生活质量和疗效参数的改善持续到第52周。赛库单抗治疗耐受性良好,未观察到新的安全信号。结论塞库单抗治疗可使相当一部分银屑病患者及其家属的生活质量完全正常化,无论他们之前是否接受过治疗。

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