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Comparative efficacy and safety of combination therapy with infliximab for Crohn's disease: a systematic review and network meta-analysis

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DOI: 10.1007/s00384-023-04378-w

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Crohn's disease; Combination therapy; Infliximab; Network meta-analysis

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Using a network meta-analysis and systematic review, this study evaluated the efficacy and safety of combination therapy and infliximab monotherapy in Crohn's disease patients. The results showed that there was no statistical difference between different combination therapies in inducing and maintaining remission. For inducing remission, infliximab + enteral nutrition ranked highest; for maintaining remission, infliximab + azathioprine ranked highest. There was no treatment that was significantly safer than the others.
PurposeThere is not enough information to position medications for the treatment of Crohn's disease (CD). Therefore, using a network meta-analysis and systematic review, we evaluated the efficacy and safety of combination therapy and infliximab (IFX) monotherapy in CD patients.MethodsWe identified randomized controlled trials (RCTs) in CD patients who were given IFX-containing combination therapy versus IFX monotherapy. Induction and maintenance of clinical remission were the efficacy outcomes, while adverse events were the safety outcomes. The surface under cumulative ranking (SUCRA) probabilities was used to assess ranking in the network meta-analysis.ResultsIn total, 15 RCTs with 1586 CD patients were included in this study. There was no statistical difference between different combination therapies in induction and maintenance of remission. In terms of inducing clinical remission, IFX + EN (SUCRA: 0.91) ranked highest; in terms of maintaining clinical remission, IFX + AZA (SUCRA: 0.85) ranked highest. There was no treatment that was significantly safer than the others. In terms of any adverse events, serious adverse events, serious infections, and infusion/injection-site reactions, IFX + AZA (SUCRA: 0.36, 0.12, 0.19, and 0.24) was ranked lowest for all risks; while IFX + MTX (SUCRA: 0.34, 0.06, 0.13, 0.08, 0.34, and 0.08) was rated lowest for risk of abdominal pain, arthralgia, headache, nausea, pyrexia, and upper respiratory tract infection.ConclusionIndirect comparisons suggested that efficacy and safety of different combination treatments are comparable in CD patients. For maintenance therapies, IFX + AZA was ranked highest for clinical remission and lowest for adverse events. Further head-to-head trials are required.

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