P784 ustekinumab 对生物技术不成熟的炎症性肠病患者的疗效

Ž. Šubic, G. Novak
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摘要

近年来,炎症性肠病(IBD)出现了多种新的治疗方案。肿瘤坏死因子α抑制剂和新型先进疗法(vedolizumab、ustekinumab (UST) 和 Janus 激酶抑制剂)相继问世。这些药物多用于肿瘤坏死因子α抑制剂之后的二线治疗,但疗效较差。有关 UST 一线治疗疗效的数据很少。我们的研究旨在评估 UST 对生物幼稚型 IBD 患者的疗效。 这项回顾性横断面队列研究纳入了所有年龄超过 18 岁、确诊为 IBD 并在一家三级 IBD 中心(斯洛文尼亚卢布尔雅那大学医学中心)接受治疗、开始接受 UST 一线治疗的患者。我们从医疗档案中回顾性地收集了患者的人口统计学特征、临床特征、UST治疗的持续性、临床疾病活动评分、C反应蛋白(CRP)、粪便钙蛋白(FC)、UST浓度和内镜评分。我们测定了治疗持续性的卡普兰-梅耶曲线。 我们共纳入了 71 名患者,其中 11 人患有溃疡性结肠炎,60 人患有克罗恩病。在一年内,88%的生物幼稚型患者能坚持使用 UST 治疗(图 1)。57.7%的患者实现了临床缓解。77.6%的患者实现了生化缓解(CRP0.05),在实现缓解的患者组中,UST的血清浓度中值(临床(5.86μg/ml)、生化(5.93μg/ml(基于 CRP)、5.63μg/ml(基于 FC)和内镜下(7.14μg/ml))与未缓解组(分别为 5.31μg/ml、3.25μg/ml、4.47μg/ml 和 4.64μg/ml)之间的差异。 对生物幼稚型 IBD 患者进行 UST 治疗显示出较高的治疗持久性,生化和内镜缓解率也很高。与在其他先进疗法之后使用UST相比,UST作为一线疗法似乎更有效。我们需要更多的前瞻性数据来证实我们的研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P784 Efficacy of ustekinumab in biologically naïve patients with Inflammatory Bowel Disease
In recent years, there are several new treatment options for inflammatory bowel disease (IBD). Tumour necrosis factor α inhibitors have been joined by novel advanced therapies (vedolizumab, ustekinumab (UST) and Janus kinase inhibitors). These drugs are mostly used as second-line treatments after tumor necrosis factor α inhibitors, with subsequent poorer efficacy. There are few data available on the efficacy of first-line treatment with UST. The aim of our study was to assess efficacy of UST in biologically naïve patients with IBD. All patients older than 18 years who had a confirmed diagnosis of IBD, treated in a tertiary IBD centre (University Medical Centre Ljubljana, Slovenia), who started first-line treatment with UST, were included in this retrospective cross-sectional cohort study. Demographics, clinical characteristics of patients, treatment persistence of UST, clinical disease activity scores, C-reactive protein (CRP), faecal calprotectin (FC), UST concentrations, and endoscopic scores were collected retrospectively in medical files. We determined a Kaplan-Meier curve of treatment persistence. We included 71 patients, 11 of which had ulcerative colitis and 60 had Crohn’s disease. Persistence of treatment with UST in biologically naïve patients is 88% at one year (Figure 1). Clinical remission was achieved in 57.7% of patients. Biochemical remission was achieved in 77.6% (CRP<5mg/ml) and 71.1% (FC<100mg/kg) of patients. Endoscopic remission (Mayo endoscopic score <2 in ulcerative colitis or absence of ulcers in Crohn’s disease) was achieved in 50.0% of patients. There was no significant difference (P>0.05) between the median serum concentrations of UST in the group of patients who achieved remission (clinical (5.86μg/ml), biochemical (5.93μg/ml based on CRP, 5.63μg/ml based on FC) and endoscopic (7.14μg/ml)) and who did not achieve remission (5.31μg/ml, 3.25μg/ml, 4.47μg/ml and 4.64μg/ml, respectively). Treatment of UST in biologically naïve IBD patients shows high treatment persistence with high biochemical and endoscopic remission rates. It appears that UST is more efficacious if used as first-line therapy compared to the use after other advanced therapies. Further prospective data are needed to confirm our findings.
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