Suppr超能文献

在一项针对银屑病患者的随机安慰剂对照试验中,按基线体重指数分层比较阿达木单抗与甲氨蝶呤或安慰剂的疗效。

Efficacy of Adalimumab Compared With Methotrexate or Placebo Stratified by Baseline BMI in a Randomized Placebo-Controlled Trial in Patients With Psoriasis.

作者信息

Prussick Ronald, Unnebrink Kristina, Valdecantos Wendell C

出版信息

J Drugs Dermatol. 2015 Aug;14(8):864-8.

Abstract

INTRODUCTION

In the Comparative Study of Humira vs Methotrexate vs Placebo In Psoriasis Patients (CHAMPION) study, significantly more patients achieved ≥75% improvement in the Psoriasis Area and Severity Index (PASI75) and ≥90% improvement (PASI90) after 16 weeks of treatment with adalimumab (80 mg at week 0, then 40 mg every other week starting at week 1) compared with methotrexate (up to 25 mg/week orally) or placebo. In this exploratory analysis, the efficacy of adalimumab was evaluated in a subset of the CHAMPION patient population stratified by baseline body mass index (BMI).

METHODS

PASI responses and Dermatology Life Quality Index (DLQI) scores through 16 weeks of treatment were examined by baseline BMI category (<25 kg/m2 [normal], 25 to <30 kg/m2 [overweight], and ≥30 kg/m2 [obese]) in patients with psoriasis with a baseline PASI total score ≥12. Treatment differences between the adalimumab and the methotrexate or placebo groups were compared using Fisher's exact test for PASI responses and 1-way analysis of variance for DLQI scores.

RESULTS

In all BMI categories, adalimumab treatment led to significantly greater rates of PASI75/90 responses at weeks 12 and 16 compared with methotrexate or placebo (P<0.05 for all). In normal weight, overweight, and obese patients at week 16, the respective PASI75 response rates were 85.0%, 85.7%, and 61.3% with adalimumab; 43.3%, 29.3%, and 26.1% with methotrexate; and 28.6%, 16.7%, and 0% with placebo. PASI90 response rates were 70.0%, 53.6%, and 35.5% with adalimumab; 26.7%, 7.3%, and 8.7% with methotrexate; and 9.5%, 16.7%, and 0% with placebo. Across all BMI subgroups, the greatest decreases in DLQI scores from baseline occurred in the adalimumab group.

CONCLUSION

Significantly higher PASI75/90 response rates and more pronounced improvements in DLQI scores at week 16 were identified in patients treated with adalimumab, compared with methotrexate or placebo, regardless of baseline BMI category.

摘要

引言

在银屑病患者中进行的修美乐(Humira)对比甲氨蝶呤对比安慰剂的比较研究(CHAMPION)中,与甲氨蝶呤(口服剂量高达25mg/周)或安慰剂相比,接受阿达木单抗(第0周80mg,然后从第1周开始每2周40mg)治疗16周后,达到银屑病面积和严重程度指数改善≥75%(PASI75)及改善≥90%(PASI90)的患者显著更多。在这项探索性分析中,在CHAMPION患者群体中按基线体重指数(BMI)分层的一个亚组中评估了阿达木单抗的疗效。

方法

在基线PASI总分≥12的银屑病患者中,按基线BMI类别(<25kg/m²[正常]、25至<30kg/m²[超重]、≥30kg/m²[肥胖])检查治疗16周期间的PASI反应和皮肤病生活质量指数(DLQI)评分。使用Fisher精确检验比较阿达木单抗与甲氨蝶呤或安慰剂组之间的PASI反应差异,并使用单因素方差分析比较DLQI评分差异。

结果

在所有BMI类别中,与甲氨蝶呤或安慰剂相比,阿达木单抗治疗在第12周和第16周导致PASI75/90反应率显著更高(所有P<0.05)。在第16周时,正常体重、超重和肥胖患者中,阿达木单抗的PASI75反应率分别为85.0%、85.7%和61.3%;甲氨蝶呤分别为43.3%、29.3%和26.1%;安慰剂分别为28.6%、16.7%和0%。阿达木单抗的PASI90反应率分别为70.0%、53.6%和35.5%;甲氨蝶呤分别为26.7%、7.3%和8.7%;安慰剂分别为9.5%、16.7%和0%。在所有BMI亚组中,DLQI评分从基线的最大降幅出现在阿达木单抗组。

结论

与甲氨蝶呤或安慰剂相比,无论基线BMI类别如何,接受阿达木单抗治疗的患者在第16周时PASI75/90反应率显著更高,DLQI评分改善更明显。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验