Table 5.
GRADE Summary of Findings reporting the comparative efficacy of different pharmacological agents for inducing clinical remission in biologic-naïve patients with moderate to severe luminal Crohn’s disease based on network meta-analysis
Medications | Relative effect (Odds ratio, 95% CI) | Overall Quality of Evidence |
---|---|---|
Selected agents vs. Infliximab | ||
Adalimumab | 0.64 (0.22–1.88) | Low (very serious imprecision) |
Certolizumab pegol | 0.23 (0.10–0.55) | Moderate (imprecision) |
Vedolizumab | 0.46 (0.16–1.26) | Low (very serious imprecision) |
Ustekinumab | 0.47 (0.19–1.12) | Low (very serious imprecision) |
Selected agents vs. Adalimumab | ||
Certolizumab pegol | 0.36 (0.15–0.86) | Moderate (imprecision) |
Vedolizumab | 0.71 (0.25–1.98) | Low (very serious imprecision) |
Ustekinumab | 0.73 (0.30–1.76) | Low (very serious imprecision) |
Selected agents vs. Certolizumab pegol | ||
Vedolizumab | 1.97 (0.88–4.41) | Low (very serious imprecision) |
Ustekinumab | 2.02 (1.09–3.75) | Moderate (imprecision) |
Selected agents vs. Vedolizumab | ||
Ustekinumab | 1.02 (0.45–2.32) | Low (very serious imprecision) |
Even though trials of infliximab used non-conventional infliximab doses or dosing regimens (one trial only used single dose, another trial treated all patients concomitantly with thiopurines), we opted not to rate down for intransitivity since effect estimates using conventional dosing regimens were likely to be more favorable