Rodríguez-Lopez Andrea, Martínez-Sendino María, Prieto-Pérez Rocío, Soria-Chacartegui Paula, González-Iglesias Eva, Aparicio-Domínguez Mario, Berenguer-Ruiz Sonsoles, Daudén Esteban, Abad-Santos Francisco
Clinical Pharmacology Department, Hospital Universitario de La Princesa, Faculty of Medicine, Universidad Autónoma de Madrid (UAM), Instituto de Investigación Sanitaria La Princesa (IP), 28006 Madrid, Spain.
Clinical Pharmacology Department, Hospital Universitario La Paz, Department of Pharmacology and Therapeutics, Faculty of Medicine, Universidad Autónoma de Madrid (UAM), IdiPAZ, 28046 Madrid, Spain.
Biomedicines. 2024 Dec 24;13(1):5. doi: 10.3390/biomedicines13010005.
: Psoriasis is a skin disease characterized by the presence of erythematous, scaly plaques on the extensor surfaces of the body. Treatment varies according to the stage of the disease, with the most severe cases being treated with biologic treatments that differ in efficacy and persistence over time. This study aimed to evaluate the 10-year persistence of biologic drugs (adalimumab, etanercept, infliximab and ustekinumab) in the treatment of moderate-to-severe plaque psoriasis. : A total of 143 patients (61 women and 82 men) were evaluated; data were collected from the electronic clinical history, and statistical analysis was performed using the SPSS program. In addition, 115 of them were genotyped in a previous study for 173 immune system genetic polymorphisms. : The persistence of biologic drugs at 10 years was 25.9% (95% CI: 17.2-34.5%). Adalimumab was the most persistent drug (41.5%), followed by ustekinumab (34.8%), infliximab (28%) and etanercept (9.3%). The main reason for discontinuation was insufficient efficacy (51%). Adalimumab allowed an increase in the dosing interval in 82.4% of patients who persisted and ustekinumab allowed an increase in 37.5%. The 10-year persistence was related to sex (higher in men, < 0.001), biologic drug ( = 0.002) and polymorphisms in (rs983332) ( = 0.014) and (rs1167846) ( = 0.013). : The results show that 25% of psoriasis patients treated with first-line biologics persisted at 10 years.
银屑病是一种皮肤病,其特征是在身体伸侧出现红斑鳞屑性斑块。治疗方法根据疾病阶段而异,最严重的病例采用生物治疗,这些生物治疗在疗效和随时间的持续性方面存在差异。本研究旨在评估生物药物(阿达木单抗、依那西普、英夫利昔单抗和乌司奴单抗)治疗中度至重度斑块状银屑病的10年持续性。
共评估了143例患者(61名女性和82名男性);数据从电子临床病史中收集,并使用SPSS程序进行统计分析。此外,其中115例在先前的一项研究中针对173种免疫系统基因多态性进行了基因分型。
生物药物10年的持续性为25.9%(95%CI:17.2 - 34.5%)。阿达木单抗是持续性最强的药物(41.5%),其次是乌司奴单抗(34.8%)、英夫利昔单抗(28%)和依那西普(9.3%)。停药的主要原因是疗效不足(51%)。在持续用药的患者中,82.4%的患者使用阿达木单抗后给药间隔得以延长,37.5%的患者使用乌司奴单抗后给药间隔得以延长。10年持续性与性别(男性更高,P<0.001)、生物药物(P = 0.002)以及IL12B(rs983332)(P = 0.014)和IL23R(rs1167846)(P = 0.013)的多态性有关。
结果表明,接受一线生物药物治疗的银屑病患者中有25%在10年后仍持续用药。