The current study compared the drug survival of ustekinumab among patients with IBD in stable remission (â„6 months) who extended their treatment interval from every 8 weeks to every 12 weeks (n=105), with that in patients who continued on an 8-week dosing regimen (n=88) [1]. âLengthening of the dosing interval occurred at the discretion of the treating physician and patient,â added Dr Monique Devillers (Erasmus MC, the Netherlands). âWe performed inverse probability of treatment weighting to correct for selection bias and confounding factors,â mentioned Dr Devillers. âThis did not impact our results and therefore I will present the unweighted results.â
The cumulative 24-week and 52-week drug survival rates of the 12-week group and 8-week group were comparable (70.2% vs 76.1%; P=0.45). In the subgroup of participants with Crohnâs disease, the corresponding rates were 74.9% and 74.6% (P=0.80). In the 12-week group, 26 participants had a so-called âdrug eventâ. Of these 26, 22 intensified their ustekinumab therapy (mostly to an 8-week regimen), 3 switched therapy, and 1 participant discontinued therapy due to a malignancy. Of note, a drug event was also reported by 21 participants in the 8-week group.
âLengthening of the ustekinumab treatment interval from 8 weeks to 12 weeks appeared to result in a comparable effectiveness in patients with stable IBD,â concluded Dr Devillers. âThese were however preliminary study results and we need to await the completed follow-up, expected in May 2025.â
- Devillers MJC, et al. Lengthening the Ustekinumab interval from every 8 weeks to every 12 weeks in IBD patients in remission. Abstract LB10, UEG Week 2024, 12â15 October, Vienna, Austria.
Medical writing support was provided by Robert van den Heuvel.
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