磁共振肠造影评估维多珠单抗治疗中重度克罗恩病的跨壁愈合:VERSIFY 3 期临床试验的可行性。

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinical and Experimental Gastroenterology Pub Date : 2024-01-27 eCollection Date: 2024-01-01 DOI:10.2147/CEG.S429039
Jordi Rimola, Jean-Frédéric Colombel, Brian Bressler, Shashi Adsul, Jenifer Siegelman, Patricia E Cole, Dirk Lindner, Silvio Danese
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引用次数: 0

摘要

目的:VERSIFY 3 期试验针对使用维多珠单抗治疗的克罗恩病(CD)患者,首次纳入了一项子研究,该研究使用标准化磁共振肠造影术(MRE)方案评估跨壁炎症特征(肠道水肿和肠壁厚度)和跨壁疾病活动特征(淋巴结肿大):患者在第0周(基线)、第2周和第6周接受静脉注射维多珠单抗(300毫克),然后在26周或52周内每8周接受一次静脉注射。事后分析包括基线时至少一个肠段的磁共振活动指数评分≥7分的亚群,以及基线后至少一次磁共振活动指数评估。对跨膜炎症(包括肠壁内水肿和肠壁厚度)的变化进行评估。结果:在基线和第 26 周,对 27 名患者的 83 个可评估肠段进行了 MRE 图像评估;在基线、第 26 周和第 52 周,对 13 名患者的 38 个可评估肠段进行了 MRE 图像评估。基线时,所有患者都有肠壁水肿,至少有一个肠段的肠壁厚度大于 3 毫米。水肿患者的比例在第26周(17/27 [63.0%])和第52周(4/13 [30.8%])时有所下降,肠壁厚度大于3毫米的患者比例在第26周(25/27 [92.6%])和第52周(10/13 [76.9%])时有所下降:结论:在接受维多珠单抗治疗26周和52周的CD患者中,MRE检测出跨壁炎症的患者人数和肠段数量均有所减少。这些结果凸显了维多珠单抗对CD患者跨壁炎症成分的影响,并证明在CD多中心临床试验中使用MRE是可行的:临床试验注册:ClinicalTrials.gov NCT02425111,2015年4月23日,http://www.clinicaltrials.gov NCT02425111;欧盟临床试验注册EudraCT 2014-003509-13,https://www.clinicaltrialsregister.eu。
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Magnetic Resonance Enterography Assessment of Transmural Healing with Vedolizumab in Moderate to Severe Crohn's Disease: Feasibility in the VERSIFY Phase 3 Clinical Trial.

Purpose: The VERSIFY phase 3 trial in patients with Crohn's disease (CD) treated with vedolizumab was the first to include a substudy that used a standardized magnetic resonance enterography (MRE) protocol to assess features of transmural inflammation (bowel edema and wall thickness) and extramural disease activity (enlarged lymph nodes).

Patients and methods: Patients received intravenous vedolizumab (300 mg) at weeks 0 (baseline), 2, and 6, and then every 8 weeks for 26 or 52 weeks. Post hoc analyses included a subpopulation with a Magnetic Resonance Index of Activity score of ≥7 in at least one bowel segment at baseline and at least one postbaseline MRE assessment. Changes in transmural inflammation, including intramural bowel edema and wall thickness, were evaluated. Patient-level and segment-level analyses were performed.

Results: MRE images were evaluated in 27 patients with 83 evaluable bowel segments at baseline and week 26, and 13 patients with 38 evaluable segments at baseline, week 26, and week 52. At baseline, all patients had bowel wall edema and wall thickness of >3 mm in at least one bowel segment. The proportion of patients with edema decreased at weeks 26 (17/27 [63.0%]) and 52 (4/13 [30.8%]) and the proportion with bowel wall thickness of >3 mm decreased at weeks 26 (25/27 [92.6%]) and 52 (10/13 [76.9%]).

Conclusion: In patients with CD treated with vedolizumab for 26 and 52 weeks, the number of patients, and bowel segments, with MRE-detected transmural inflammation was reduced. These results highlight the impact of vedolizumab on components of transmural inflammation in CD and demonstrate that using MRE in CD multicenter clinical trials is feasible.

Trial registration: ClinicalTrials.gov NCT02425111, April 23, 2015, http://www.clinicaltrials.gov NCT02425111; EU Clinical Trials Register EudraCT 2014-003509-13, https://www.clinicaltrialsregister.eu.

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来源期刊
Clinical and Experimental Gastroenterology
Clinical and Experimental Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
5.10
自引率
0.00%
发文量
26
审稿时长
16 weeks
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