Real-world effectiveness of risankizumab in psoriasis: first Sardinian multicenter 2-year experience.

IF 2.1 4区 医学 Q3 DERMATOLOGY
Grazia Vivanet, Giacomo Bertolino, Cristina Mugheddu, Gabriele Biondi, Gianmario Addis, Giovanni M Carcassi, Pietro Aste, Rosanna Satta, Maria Grazia Mugoni, Elisabetta Scotti, Maria G Atzori, Maria A Montesu, Laura Atzori
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引用次数: 0

Abstract

Background: Psoriasis is an immune-mediated chronic skin disease associated with multiple extracutaneous comorbidities, causing a severe quality of life impairment, whose treatment with risankizumab, a humanized anti-IL-23 monoclonal antibody, is very effective, with good safety profile and long-term outcomes. However, prescription in a real-world setting is conditioned by local health care system constraints, as the proven ineffectiveness or appearance of adverse events to first-line drugs. Such delay and selection of multi-failure patients might affect efficacy and outcomes.

Methods: A prospective multicenter study, approved by the Ethical Independent Committee of AOU Cagliari, acronym ESSOS-BIO-PSO, Prot N° 2023/2532, was conducted to evaluate risankizumab's effectiveness and safety in Sardinian psoriasis centers over 6, 12, and 24 months.

Results: 73 patients with moderate-to-severe psoriasis treated with risankizumab over at least 6 months were recruited, predominantly male (70%) with a median age of 50 years and a median disease duration of 22 years. Most patients had extensive, difficult-to-treat areas involved, psoriasis arthritis and other comorbidities. Prior treatments included traditional systemic therapies and biologics (60%). At week 52, 74% achieved PASI-90, increasing to 76.7% at week 104, with all initial PASI-90 responders maintaining the response. Faster and sustained responses were observed in biologic-naïve patients and those with shorter disease duration. The difference between groups was statistically significant at week 16 (Mann-Whitney P=0.042), identifying naïve patients as "super-responders." No severe adverse events occurred; risankizumab was well tolerated and adherence was 100%.

Conclusions: This real-world study investigates effectiveness and safety of Risankizumab in a population with a distinctive historical and genetic background, as well as environmental factors which may influence disease patterns and response to treatments. This first Sardinian study confirms durable results with excellent adherence in moderate-to-severe psoriasis patients, regardless of prior treatments and comorbidities burden, although in biologic-naïve patients the response is quicker.

risankizumab治疗牛皮癣的实际有效性:第一个撒丁岛多中心2年经验。
背景:银屑病是一种免疫介导的慢性皮肤病,与多种皮外合并症相关,可导致严重的生活质量损害,使用人源化抗il -23单克隆抗体risankizumab治疗银屑病非常有效,具有良好的安全性和长期结果。然而,在现实世界中,处方受到当地卫生保健系统的限制,如一线药物被证明无效或出现不良事件。这种延误和选择多重衰竭患者可能会影响疗效和预后。方法:通过AOU Cagliari伦理独立委员会(首字母缩写为ESSOS-BIO-PSO, Prot N°2023/2532)批准的一项前瞻性多中心研究,评估risankizumab在撒丁岛银屑病中心6、12和24个月的有效性和安全性。结果:招募了73例接受利桑单抗治疗至少6个月的中重度牛皮癣患者,主要是男性(70%),中位年龄为50岁,中位病程为22年。大多数患者有广泛的、难以治疗的受累区域、牛皮癣、关节炎和其他合并症。既往治疗包括传统的全身治疗和生物制剂(60%)。在第52周,74%的患者达到了PASI-90,在第104周增加到76.7%,所有最初的PASI-90应答者都保持了应答。在biologic-naïve患者和病程较短的患者中观察到更快和持续的反应。在第16周,两组之间的差异具有统计学意义(Mann-Whitney P=0.042),确定naïve患者为“超级应答者”。未发生严重不良事件;利桑单抗耐受性良好,依从性为100%。结论:这项现实世界的研究调查了Risankizumab在具有独特历史和遗传背景的人群中的有效性和安全性,以及可能影响疾病模式和对治疗反应的环境因素。这是撒丁岛的第一项研究,证实了在中重度牛皮癣患者中具有优异依从性的持久结果,无论先前的治疗和合并症负担如何,尽管在biologic-naïve患者中反应更快。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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