Department of Medicine [Division of Gastroenterology] and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, ON, Canada.
Department of Medicine, Division of Gastroenterology, Western University, London, ON, Canada.
J Crohns Colitis. 2024 Nov 4;18(11):1863-1869. doi: 10.1093/ecco-jcc/jjae092.
It is unclear if steroid tapering protocols can affect clinical trial outcomes in ulcerative colitis [UC], particularly fixed versus adaptive steroid tapering. Fixed steroid tapering involves incremental dose decreases at prespecified intervals, and adaptive steroid tapering uses investigator discretion as determined by the patient's response.
In this post-hoc analysis from six clinical trials of UC [VARSITY, ACT 1, PURSUIT, GEMINI1, OCTAVE, and ULTRA2], responders to induction therapy with baseline corticosteroid use were considered as the primary population of interest. Adjustments were made to account for treat-through versus re-randomisation designs, and multivariate regression was performed to account for other potential confounding variables. The primary outcome was corticosteroid-free clinical remission [CR] at 1 year, and secondary outcomes were CR and endoscopic improvement.
There was a total of 861 patients who had achieved clinical response after induction and were using corticosteroids. Within multivariate analysis, patients using adaptive steroid tapering regimens were less likely to achieve corticosteroid-free CR at 1 year (odds ratio [OR] 0.66 [95% confidence interval, CI, 0.48-0.92], p = 0.015) but had increased odds for achieving CR at 1 year (OR 1.9 [95% CI 1.43-2.52], p < 0.001). The steroid tapering regimen was not associated with achievement of endoscopic improvement at 1 year.
Among patients with UC on corticosteroids in clinical trials, patients using adaptive steroid weaning regimens were less likely to achieve corticosteroid-free CR at 1 year but more likely to achieve CR at 1 year. Consideration should be given to implementing mandatory fixed steroid weaning protocols in future clinical trials of UC.
目前尚不清楚类固醇逐渐减量方案是否会影响溃疡性结肠炎[UC]的临床试验结果,特别是固定方案与适应性方案。固定剂量的类固醇逐渐减量方案涉及在预定间隔内逐步减少剂量,而适应性类固醇逐渐减量方案则根据患者的反应由研究者自行决定。
在这项来自六个 UC 临床试验的事后分析[VARSITY、ACT 1、PURSUIT、GEMINI1、OCTAVE 和 ULTRA2]中,将诱导治疗后使用基线皮质类固醇的应答者视为主要关注人群。调整了治疗贯穿与重新随机设计,并进行多变量回归以考虑其他潜在的混杂变量。主要结局是 1 年内无皮质类固醇的临床缓解[CR],次要结局是 CR 和内镜改善。
共有 861 名患者在诱导后达到临床缓解并使用皮质类固醇。在多变量分析中,使用适应性类固醇逐渐减量方案的患者在 1 年内达到无皮质类固醇 CR 的可能性较小(比值比[OR] 0.66 [95%置信区间,CI,0.48-0.92],p=0.015),但在 1 年内达到 CR 的可能性更高(OR 1.9 [95%CI 1.43-2.52],p<0.001)。类固醇逐渐减量方案与 1 年内内镜改善无关。
在临床试验中接受皮质类固醇治疗的 UC 患者中,使用适应性类固醇逐渐减量方案的患者在 1 年内达到无皮质类固醇 CR 的可能性较小,但在 1 年内达到 CR 的可能性更大。在未来的 UC 临床试验中,应考虑实施强制性固定类固醇逐渐减量方案。