Division of Gastroenterology, Department of Medicine, University of Washington, Seattle, WA, United States; Inflammatory Bowel Disease Program, University of Washington Medical Center, Seattle, WA, United States.
Inflammatory Bowel Disease Program, University of Washington Medical Center, Seattle, WA, United States.
J Crohns Colitis. 2014 Jun;8(6):480-8. doi: 10.1016/j.crohns.2013.10.013. Epub 2013 Nov 21.
BACKGROUND & AIMS: Anti-tumor necrosis factors (anti-TNF) including infliximab, adalimumab and certolizumab pegol are used to treat Crohn's disease (CD) and ulcerative colitis (UC). Paradoxically, while also indicated for the treatment of psoriasis, anti-TNF therapy has been associated with development of psoriasiform lesions in IBD patients and can compel discontinuation of therapy. We aim to investigate IBD patient, clinical characteristics, and frequency for the development of and outcomes associated with anti-TNF induced psoriasiform rash.
We identify IBD patients on anti-TNFs with an onset of a psoriasiform rash. Patient characteristics, duration of anti-TNF, concomitant immunosuppressants, lesion distribution, and outcomes of rash are described.
Of 1004 IBD patients with exposure to anti-TNF therapy, 27 patients (2.7%) developed psoriasiform lesions. Psoriasiform rash cases stratified by biologic use were 1.3% for infliximab, 4.1% for adalimumab, and 6.4% for certolizumab. Average time on treatment (206.3weeks) and time on treatment until onset of psoriasiform lesions (126.9weeks) was significantly higher in the infliximab group. The adalimumab group had the highest need for treatment discontinuation (60%). The majority (59.3%) of patients were able to maintain on anti-TNFs despite rash onset. Among patients that required discontinuation (40.7%), the majority experienced improvement with a subsequent anti-TNF (66.7%).
27 cases of anti-TNF associated psoriasiform lesions are reported. Discontinuation of anti-TNF treatment is unnecessary in the majority. Dermatologic improvement was achieved in the majority with a subsequent anti-TNF, suggesting anti-TNF induced psoriasiform rash is not necessarily a class effect.
抗肿瘤坏死因子(anti-TNF)包括英夫利昔单抗、阿达木单抗和培塞利珠单抗,用于治疗克罗恩病(CD)和溃疡性结肠炎(UC)。具有讽刺意味的是,尽管抗 TNF 治疗也被用于治疗银屑病,但在 IBD 患者中,它与银屑病样病变的发展有关,并可能迫使停止治疗。我们旨在研究 IBD 患者的临床特征、抗 TNF 诱导的银屑病样皮疹的发病频率及相关结局。
我们确定了使用抗 TNF 治疗且出现银屑病样皮疹的 IBD 患者。描述了患者特征、抗 TNF 治疗时间、同时使用的免疫抑制剂、病变分布以及皮疹的结局。
在接受抗 TNF 治疗的 1004 例 IBD 患者中,有 27 例(2.7%)出现银屑病样病变。按生物制剂分类的银屑病样皮疹病例分别为英夫利昔单抗 1.3%、阿达木单抗 4.1%和培塞利珠单抗 6.4%。英夫利昔单抗组的治疗时间(206.3 周)和治疗开始至出现银屑病样病变的时间(126.9 周)明显更长。阿达木单抗组的治疗停药率最高(60%)。大多数(59.3%)患者尽管出现皮疹仍能继续使用抗 TNF 治疗。需要停药的患者(40.7%)中,大多数(66.7%)在使用后续抗 TNF 治疗后病情改善。
报告了 27 例抗 TNF 相关的银屑病样病变。大多数患者不需要停止抗 TNF 治疗。大多数患者在使用后续抗 TNF 治疗后皮肤疾病得到改善,这表明抗 TNF 诱导的银屑病样皮疹不一定是一种类效应。