Armstrong April W, Soliman Ahmed M, Gisondi Paolo, Fang Siran, Patel Manish, Strober Bruce
Department of Dermatology, Keck School of Medicine, University of Southern California, 1450 San Pablo St #5400, Los Angeles, CA, 90033, USA.
AbbVie Inc., North Chicago, IL, USA.
Dermatol Ther (Heidelb). 2024 Nov;14(11):3071-3081. doi: 10.1007/s13555-024-01293-y. Epub 2024 Oct 25.
Despite advancements in the treatment of psoriasis (PsO), there are few head-to-head studies assessing comparative effectiveness of the newest therapies approved to treat PsO. Our objective was to assess the comparative clinical effectiveness of risankizumab and deucravacitinib in patients with moderate-to-severe PsO.
This placebo-anchored matching-adjusted indirect comparison (MAIC) analysis utilized data from UltIMMa-1/2 risankizumab and POETYK PSO-1/2 deucravacitinib trials. Individual patient data from UltiMMA-1/2 were weighted via propensity score to match POETYK PSO-1/2 published summary data. Rate differences between risankizumab and deucravacitinib were assessed for Psoriasis Area and Severity Index (PASI) 75/90/100, the Static Physician Global Assessment (sPGA = 0 or 0/1), and the Dermatology Life Quality Index (DLQI) 0/1.
At 16 weeks, risankizumab-treated patients demonstrated statistically significantly higher rates of skin clearance and greater improvement in quality of life (QoL) compared to those treated with deucravacitinib. Across all outcomes, risankizumab demonstrated a lower number needed to treat compared to deucravacitinib. Limitations are potential bias due to unobserved/unmeasurable differences and limited generalizability of the results.
This indirect comparison demonstrates that risankizumab has higher rates of skin clearance and greater improvements in QoL than deucravacitinib. This study will help inform healthcare providers in their treatment and management strategy of PsO.
尽管银屑病(PsO)的治疗取得了进展,但评估批准用于治疗PsO的最新疗法的相对有效性的直接对比研究却很少。我们的目的是评估司库奇尤单抗和氘可来昔替尼在中度至重度PsO患者中的相对临床有效性。
这项以安慰剂为对照的匹配调整间接比较(MAIC)分析使用了UltIMMa-1/2司库奇尤单抗试验和POETYK PSO-1/2氘可来昔替尼试验的数据。通过倾向评分对UltIMMa-1/2的个体患者数据进行加权,以匹配POETYK PSO-1/2公布的汇总数据。评估司库奇尤单抗和氘可来昔替尼在银屑病面积和严重程度指数(PASI)75/90/100、静态医师整体评估(sPGA = 0或0/1)以及皮肤病生活质量指数(DLQI)0/1方面的率差。
在16周时,与接受氘可来昔替尼治疗的患者相比,接受司库奇尤单抗治疗的患者皮肤清除率在统计学上显著更高,生活质量(QoL)改善更大。在所有结局指标中,司库奇尤单抗的治疗所需人数低于氘可来昔替尼。局限性在于可能存在因未观察到/无法测量的差异导致的偏倚以及结果的普遍性有限。
这项间接比较表明,司库奇尤单抗的皮肤清除率高于氘可来昔替尼,且在QoL方面改善更大。这项研究将有助于为医疗保健提供者制定PsO的治疗和管理策略提供参考。