Olivera Pablo A, Lasa Juan S, Zubiaurre Ignacio, Jairath Vipul, Abreu Maria T, Rubin David T, Reinisch Walter, Magro Fernando, Rahier Jean-François, Danese Silvio, Rabaud Christian, Peyrin-Biroulet Laurent
IBD Unit, Gastroenterology Section, Department of Internal Medicine, Centro de Educación Médica e Investigación Clínica (CEMIC), Buenos Aires, Argentina.
Zane Cohen Centre for Digestive Diseases, Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON, Canada.
J Crohns Colitis. 2023 Mar 18;17(2):199-210. doi: 10.1093/ecco-jcc/jjac133.
Advanced therapies for inflammatory bowel disease [IBD] could potentially lead to a state of immunosuppression with an increased risk of opportunistic infections [OIs]. We aimed to provide an update on the incidence of OIs among adult IBD patients in randomized controlled trials [RCTs] of approved biologics and small-molecule drugs [SMDs]. Also, we aimed to describe OI definitions utilized in RCTs, to ultimately propose a standardized definition.
Electronic databases were searched from January 1, 1990, until April 16, 2022. Our primary outcome was incidence rate of overall OIs among IBD patients exposed and unexposed to biologics or SMDs. We also describe specific OIs reported in included trials, as well as definitions of OIs within studies when provided.
Ninety studies were included. The incidence rates of reported OIs were 0.42 and 0.21 per 100 person-years in patients exposed to advanced therapies and placebo, respectively. This was highest for anti-tumour necrosis factors [0.83 per 100 person-years] and Janus kinase inhibitors [0.55 per 100 person-years] and lowest for anti-integrins and ozanimod. On meta-analysis, no increased risk of OIs was observed. None of the studies provided a detailed definition of OIs, or a comprehensive list of infections considered as OIs.
Different mechanisms of action may have specific OI profiles. In the absence of a uniform definition of OIs, these estimates are less reliable. We propose a definition to be used in future studies to help provide standardized reporting. When using this definition, we saw significant differences in incidence rates of OIs across mechanisms of action.
炎症性肠病(IBD)的先进疗法可能会导致免疫抑制状态,增加机会性感染(OI)风险。我们旨在更新已获批生物制剂和小分子药物(SMD)的随机对照试验(RCT)中成年IBD患者的OI发生率。此外,我们旨在描述RCT中使用的OI定义,最终提出一个标准化定义。
检索了1990年1月1日至2022年4月16日的电子数据库。我们的主要结局是暴露于生物制剂或SMD与未暴露的IBD患者中总体OI的发生率。我们还描述了纳入试验中报告的特定OI,以及研究中提供的OI定义。
纳入了90项研究。接受先进疗法和安慰剂的患者中,报告的OI发生率分别为每100人年0.42和0.21。这在抗肿瘤坏死因子(每100人年0.83)和Janus激酶抑制剂(每100人年0.55)中最高,在抗整合素和奥扎尼莫德中最低。荟萃分析未观察到OI风险增加。没有研究提供OI的详细定义,或被视为OI的感染综合列表。
不同的作用机制可能有特定的OI特征。在缺乏OI统一定义的情况下,这些估计不太可靠。我们提出一个定义供未来研究使用,以帮助提供标准化报告。使用这个定义时,我们发现不同作用机制的OI发生率存在显著差异。