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首页> 外文期刊>British Journal of Dermatology >Ustekinumab improves health-related quality of life in patients with moderate-to-severe psoriasis: results from the PHOENIX 1 trial.
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Ustekinumab improves health-related quality of life in patients with moderate-to-severe psoriasis: results from the PHOENIX 1 trial.

机译:Ustekinumab改善中重度牛皮癣患者的健康相关生活质量:PHOENIX 1试验的结果。

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Background PHOENIX 1 was a phase III, randomized, double-blind, placebo-controlled study that demonstrated the long-term efficacy and safety of ustekinumab in patients with moderate-to-severe psoriasis. Objectives To assess the effect of ustekinumab maintenance therapy on health-related quality of life (HRQoL) in PHOENIX 1 patients. Patients and methods Patients (n = 766) were randomized to receive ustekinumab 45 mg (n = 255) or 90 mg (n = 256) at weeks 0 and 4 and every 12 weeks thereafter, or placebo (n = 255) at weeks 0 and 4 with crossover to ustekinumab at week 12. Ustekinumab-randomized patients achieving at least 75% improvement in Psoriasis Area and Severity Index (PASI) 75 at weeks 28 and 40 were re-randomized at week 40 to continue ustekinumab or be withdrawn until loss of therapeutic effect. HRQoL was assessed using the SF-36 and Dermatology Life Quality Index (DLQI). Results At baseline, more than 97% had a DLQI > 1 and the average DLQI was > 10, indicating a significant impact on patients' HRQoL. Significantly greater proportions of patients receiving ustekinumab 45 and 90 mg achieved a normalized DLQI score (< or = 1) compared with placebo (53.2%, 52.4% and 6.0%, respectively, both P < 0.001) at week 12 and achieved a clinically meaningful improvement (increase of at least five points) in SF-36 physical (23.1%, 33.7% and 15.6%) and mental (25.5%, 31.3% and 14.8%) component summary scores. At week 12, changes in individual DLQI and SF-36 domains were significantly better in each ustekinumab group vs. placebo (P < 0.001). The magnitude of improvement across SF-36 scales was greatest for the bodily pain and social functioning domains. Improvements in HRQoL were sustained with maintenance ustekinumab therapy through at least 1 year. Regression analysis showed that, after adjustment for improvement in PASI or Physician's Global Assessment (PGA), ustekinumab-treated patients demonstrated significant improvements in DLQI. Conclusions Ustekinumab improves HRQoL in patients with moderate-to-severe psoriasis. Patient-reported outcomes measured a treatment effect beyond that indicated by clinical measures.
机译:背景PHOENIX 1是一项III期,随机,双盲,安慰剂对照研究,证实了ustekinumab在中至重度牛皮癣患者中的长期疗效和安全性。目的评估乌斯他单抗维持治疗对PHOENIX 1患者健康相关生活质量(HRQoL)的影响。患者和方法患者(n = 766)被随机分配在第0和4周以及此后每12周接受45 mg(n = 255)或90 mg(n = 256)的ustekinumab,或在第0周接受安慰剂(n = 255)。和4位患者在第12周转用ustekinumab。在第28周和第40周时,ustekinumab随机分组的患者在牛皮癣面积和严重性指数(PASI)75方面至少提高了75%,在第40周重新随机分组以继续使用ustekinumab或撤回直至丢失有治疗作用。使用SF-36和皮肤病生活质量指数(DLQI)评估HRQoL。结果基线时,有超过97%的DLQI> 1,平均DLQI> 10,表明对患者的HRQoL有显着影响。与安慰剂组(分别为53.2%,52.4%和6.0%,二者均P <0.001)相比,接受乌斯替单抗45和90 mg的患者达到标准化DLQI评分(<或= 1)的比例显着更高,并且具有临床意义SF-36身体(23.1%,33.7%和15.6%)和精神(25.5%,31.3%和14.8%)组成部分总成绩的改善(至少提高了5分)。在第12周时,每个ustekinumab组的单个DLQI和SF-36结构域的变化均显着好于安慰剂组(P <0.001)。 SF-36量表的改善幅度最大,适用于身体疼痛和社交功能领域。维持乌斯库单抗治疗至少一年可维持HRQoL的改善。回归分析表明,在调整了PASI或医生的整体评估(PGA)的改善后,乌斯他单抗治疗的患者表现出DLQI的显着改善。结论Ustekinumab可改善中度至重度牛皮癣患者的HRQoL。患者报告的结局所衡量的治疗效果超出了临床指标。

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