P886 Ustekinumab concentrations in induction are associated with mid-term endoscopic outcomes in patients with inflammatory bowel disease

X Serra-Ruiz, E Céspedes Martínez, L Mayorga Ayala, C Herrera de-Guise, V Robles Alonso, Z Pérez Martínez, E Oller, N Borruel Sainz
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Abstract

Background It is unclear whether ustekinumab (UST) concentrations can predict the clinical course of inflammatory bowel disease (IBD) and guide treatment algorithms during the induction phase. The aim of our study was to assess the association between serum UST concentrations during the induction phase and clinical outcomes at week 24 and to determine the validity of a UST threshold for guiding intensification strategies. Methods We conducted a retrospective study including Crohn's disease (CD) and ulcerative colitis (UC) patients who started UST treatment between June 2022 and February 2023. Intensification strategies were determined according to standard clinical practice. UST concentrations were collected at weeks 8, 16, and 24. Quartile analysis and logistic regression were performed to evaluate the association between UST concentrations and treatment targets. Definitions are clinical steroid-free remission as a Harvey-Bradshaw index <5 and a partial Mayo score <2; endoscopic remission as a simple endoscopic score (SES-CD) ≤2 and Mayo endoscopic score (EMS) ≤1; and endoscopic response as a ≥50% reduction in SES-CD and ≥1 point in EMS. Results We included 42 patients (CD: 24). At week 24, clinical remission rates of 67% and endoscopic response and remission rates of 57% and 28%, respectively, were achieved. At week 24, the majority of patients continued intensified treatment: 90 mg subcutaneously every 4 weeks in 55% and 130 mg intravenously every 4 weeks in 36%. Patients who achieved an endoscopic response at week 24 had higher UST levels at week 8 (4.1 vs. 2.9 µg/ml, p=0.029). No significant differences between endoscopic remission rates and UST levels at any week were observed. The differences observed in the quartile analysis between the UST concentrations at week 8 and the endoscopic response were not statistically significant (p=0.451). The area under the ROC curve value for UST levels at week 8 to predict endoscopic response was 0.734 (p=0.012). Logistic regression analysis identified prior exposure to vedolizumab and absence of perianal disease as predictors of endoscopic response and remission at week 24 in univariate analysis, but not in multivariate analysis. No association was observed between UST levels and drug persistence rates. Conclusion In this real-world cohort, higher UST concentrations at week 8 were associated with higher rates of endoscopic response at week 24. A reliable concentration threshold for predicting endoscopic response and treatment intensification could not be determined, probably due to the insufficient number of patients included in the study and the relatively poor performance of the ROC curve. Prospective, randomized studies are needed to validate these results.
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P886 Ustekinumab在诱导过程中的浓度与炎症性肠病患者的中期内镜检查结果有关
背景 目前尚不清楚乌司替单抗(UST)浓度能否预测炎症性肠病(IBD)的临床过程并指导诱导期的治疗算法。我们的研究旨在评估诱导期血清 UST 浓度与第 24 周临床结果之间的关联,并确定 UST 阈值对指导强化策略的有效性。方法 我们进行了一项回顾性研究,研究对象包括在 2022 年 6 月至 2023 年 2 月期间开始 UST 治疗的克罗恩病(CD)和溃疡性结肠炎(UC)患者。根据标准临床实践确定了强化策略。在第 8、16 和 24 周收集 UST 浓度。采用四分位分析和逻辑回归评估 UST 浓度与治疗目标之间的关联。定义为临床无类固醇缓解为哈维-布拉德肖指数(Harvey-Bradshaw index)<5,部分梅奥评分(Mayo score)<2;内镜缓解为单纯内镜评分(SES-CD)≤2,梅奥内镜评分(EMS)≤1;内镜反应为 SES-CD 降低≥50%,EMS 降低≥1 分。结果 我们共纳入 42 例患者(CD:24 例)。第24周时,临床缓解率为67%,内镜反应和缓解率分别为57%和28%。第24周时,大多数患者继续加强治疗:55%的患者每4周皮下注射90毫克,36%的患者每4周静脉注射130毫克。在第24周获得内镜反应的患者在第8周时的UST水平较高(4.1 vs. 2.9 µg/ml,p=0.029)。内镜缓解率与任何一周的 UST 水平之间均无明显差异。在第 8 周 UST 浓度与内镜反应之间的四分位分析中观察到的差异无统计学意义(p=0.451)。第 8 周 UST 浓度预测内镜反应的 ROC 曲线下面积值为 0.734(p=0.012)。逻辑回归分析表明,在单变量分析中,曾接触过维多利珠单抗和无肛周疾病是第24周内镜反应和缓解的预测因素,但在多变量分析中却不是。未观察到 UST 水平与药物持续率之间存在关联。结论 在这个真实世界队列中,第 8 周 UST 浓度越高,第 24 周的内镜反应率越高。预测内镜反应和加强治疗的可靠浓度阈值无法确定,这可能是由于研究中纳入的患者人数不足,以及 ROC 曲线的表现相对较差。需要进行前瞻性的随机研究来验证这些结果。
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