Department of Gastroenterology, Lyell McEwin Hospital, Adelaide, South Australia, Australia.
Department of Dermatology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
Intern Med J. 2023 Oct;53(10):1854-1865. doi: 10.1111/imj.15859. Epub 2022 Sep 30.
Anti-tumour necrosis factor alpha (anti-TNF) agents are a highly effective treatment for inflammatory bowel disease (IBD). Skin lesions, including psoriasiform, eczematous and lupoid eruptions, may paradoxically result from anti-TNF use and cause significant morbidity leading to discontinuation of therapy. There are no consensus guidelines on the management of these lesions.
This systematic review considers the existing evidence regarding cutaneous complications of anti-TNF therapy in IBD and the development of an algorithm for management.
A systematic review was performed by searching Medline (Pubmed) and Embase for articles published from inception to January 2021. The following search terms were used 'anti-tumour necrosis factor alpha', 'infliximab', 'adalimumab', 'certolizumab', 'golimumab', 'inflammatory bowel disease', 'Crohn disease', 'Ulcerative colitis', 'psoriasis', 'psoriasiform', 'dermatitis', 'lupus', 'skin lesion' and 'skin rash'. Reference lists of relevant studies were reviewed to identify additional suitable studies.
Thirty-four studies were included in the review. Eczema can generally be managed with topical agents and the anti-TNF can be continued, while the development of lupus requires immediate cessation of the anti-TNF and consideration of alternative immunomodulators. Management of psoriasis and psoriasiform lesions may follow a step-wise algorithm where topical treatments will be trialled in less severe cases, with recourse to an alternative anti-TNF or a switch to an alternative class of biological agent.
Assessment of anti-TNF skin lesions should be performed in conjunction with a dermatologist and rheumatologist in complex cases. High-quality prospective studies are needed to clarify the validity of these algorithms in the future.
抗肿瘤坏死因子 α(anti-TNF)制剂是治疗炎症性肠病(IBD)的一种非常有效的方法。皮肤病变,包括银屑病样、湿疹样和狼疮样皮疹,可能会因抗 TNF 治疗而出现,导致显著的发病率,从而导致治疗中断。目前尚无关于这些病变管理的共识指南。
本系统评价考虑了抗 TNF 治疗 IBD 时皮肤并发症的现有证据,并制定了管理算法。
通过搜索 Medline(Pubmed)和 Embase 数据库,检索自成立至 2021 年 1 月发表的文章,使用以下搜索词:“anti-tumour necrosis factor alpha”、“infliximab”、“adalimumab”、“certolizumab”、“golimumab”、“inflammatory bowel disease”、“Crohn disease”、“Ulcerative colitis”、“psoriasis”、“psoriasiform”、“dermatitis”、“lupus”、“skin lesion”和“skin rash”。还查阅了相关研究的参考文献,以确定其他合适的研究。
本综述共纳入 34 项研究。一般来说,湿疹可以通过局部治疗药物来控制,同时可以继续使用抗 TNF 治疗;而狼疮的发生则需要立即停止使用抗 TNF,并考虑使用其他免疫调节剂。银屑病和银屑病样病变的治疗可以遵循一个逐步的算法,在病情较轻的情况下,可以先试用局部治疗,如果效果不佳,可以考虑换用其他抗 TNF 药物或切换到其他类别的生物制剂。
在复杂的情况下,应与皮肤科医生和风湿病医生一起评估抗 TNF 皮肤病变。需要高质量的前瞻性研究来明确这些算法在未来的有效性。