Immunomodulators and advanced therapies for induction of remission in Crohn’s disease: a systematic review and network meta-analysis

Sinopoulou, Vasiliki orcid iconORCID: 0000-0002-2831-9406, Gordon, Morris orcid iconORCID: 0000-0002-1216-5158, Liu, Shiyao orcid iconORCID: 0000-0002-5245-1810, Arruda Navarro albuquerque, Daniel orcid iconORCID: 0000-0003-1539-8798, Ajiboye, Aderonke, Vuyyuru, Sudheer Kumar, Radford, Shellie and Moran, Gordon (2025) Immunomodulators and advanced therapies for induction of remission in Crohn’s disease: a systematic review and network meta-analysis. Inflammatory Bowel Diseases . ISSN 1078-0998

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Official URL: http://doi.org/10.1093/ibd/izaf191

Abstract

Background: Previous reviews for CD treatment have rarely considered advanced and immunomodulator medical therapies together. Our aim was to compare all therapies for efficacy and safety in induction of remission.

Methods: We searched databases up to June 2025. Our outcomes were clinical remission and response, endoscopic remission, and safety outcomes. We performed network meta-analyses and estimated RR and 95% CI. We used GRADE to assess certainty of results, and SUCRA for ranking treatments.

Results: A total of 79 RCTs with 20724 participants were included. Interventions ranged from two to 30 weeks. There was moderate GRADE certainty of effectiveness over placebo for clinical remission for combination of adalimumab with thiopurines (RR 2.87, 95%CI 1.99-4.14, RD=35.3%, NNT=3, large magnitude), guselkumab (RR 2.5, 95%CI 1.95-3.21, RD=28.4%, NNT=4, moderate magnitude, adalimumab (RR 2.46, 95%CI 1.84-3.29, RD=27.6% NNT=4, moderate magnitude), combination of infliximab with thiopurines (RR 2.43, 95%CI 1.71-3.44, RD=27%, NNT=4, moderate magnitude), and ustekinumab (RR 2.04, 95%CI 1.69-2.46, RD=19.6% NNT=5, small magnitude). For endoscopic remission there was moderate GRADE certainty of effectiveness for risankizumab (RR 3.48, 95%CI 2.18-5.58, RD=17.4%, moderate magnitude). The certainty on safety varied, but treatments appear generally safe short-term.

Conclusion: Combination of anti-TNFs and immunomodulators followed by anti-TNF monotherapy had large effect size with moderate certainty for the induction of clinical remission. More novel therapies appear to have similar effect sizes, but with increased imprecision of the estimates.


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