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真实世界中前瞻性斑块状银屑病患儿队列中使用甲氨蝶呤的情况:疗效、不良事件和叶酸方案。

Real-world Methotrexate Use in a Prospective Cohort of Paediatric Patients with Plaque Psoriasis: Effectiveness, Adverse Events and Folic Acid Regimen.

机构信息

Department of Dermatology, Radboud university medical centre, René Descartesdreef 1, PO Box 9101, NL-6500 HB, The Netherlands.

出版信息

Acta Derm Venereol. 2022 Jun 29;102:adv00745. doi: 10.2340/actadv.v102.1000.

Abstract

In paediatric psoriasis, few studies have evaluated methotrexate effectiveness, adverse events and folic acid regimen. Therefore this study prospectively assessed methotrexate adverse events and effectiveness in paediatric patients with psoriasis in a real-world setting. Furthermore, gastrointestinal adverse events and methotrexate effectiveness were compared between folic acid regimens (5 mg once weekly vs 1 mg 6 times weekly). Data for paediatric patients with psoriasis treated with methotrexate from September 2008 to October 2020 were extracted from Child-CAPTURE, a prospective, daily clinical practice registry. Effectiveness was determined by Psoriasis Area and Severity Index (PASI). Comparison of persistent gastrointestinal adverse events between folic acid regimens were assessed through Kaplan-Meier analysis. A total of 105 paediatric patients with plaque psoriasis (41.0% male, mean age 14.1 years) were included. At week 24 and 48, an absolute PASI ≤ 2.0 was achieved by approximately one-third of all patients. During follow-up, 46.7% reported ≥ 1 persistent adverse events. After 1 and 2 years, approximately one-quarter of patients achieved a PASI ≤ 2.0 without persistent adverse events. Although non-significant, a possible trend towards lower occurrence of gastrointestinal adverse events was found for folic acid 1 mg 6 times weekly (p = 0.196), with similar effectiveness between folic acid regimens. These findings show that a subgroup of paediatric patients with psoriasis responded well to methotrexate treatment without considerable side-effects during a 2-year follow-up.

摘要

在儿科银屑病中,很少有研究评估过甲氨蝶呤的疗效、不良反应和叶酸方案。因此,本研究前瞻性评估了真实环境中儿科银屑病患者使用甲氨蝶呤的不良反应和疗效。此外,我们比较了叶酸方案(每周 5 毫克 1 次与每周 6 次 1 毫克)之间的胃肠道不良反应和甲氨蝶呤疗效。从 2008 年 9 月至 2020 年 10 月,从 Child-CAPTURE(一个前瞻性的日常临床实践登记处)中提取了接受甲氨蝶呤治疗的儿科银屑病患者的数据。疗效通过银屑病面积和严重程度指数(PASI)来确定。通过 Kaplan-Meier 分析评估了叶酸方案之间持续性胃肠道不良反应的比较。共纳入 105 例斑块状银屑病患儿(男性 41.0%,平均年龄 14.1 岁)。在第 24 周和第 48 周,约三分之一的患者 PASI 绝对值≤2.0。在随访期间,46.7%的患者报告≥1 种持续性不良反应。在 1 年和 2 年后,约四分之一的患者 PASI≤2.0 且无持续性不良反应。尽管无统计学意义,但每周 6 次 1 毫克叶酸组胃肠道不良反应的发生率可能较低(p=0.196),且两种叶酸方案的疗效相似。这些发现表明,在 2 年的随访中,亚组儿科银屑病患者对甲氨蝶呤治疗反应良好,且副作用不大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b9b/9558319/86ddff7c0ea4/ActaDV-102-1000-g001.jpg

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