P696 Initiation of Vedolizumab did not provoke new-onset spondylarthritis in patients with inflammatory bowel disease: A Prospective Study Including Rheumatological and Blinded Imaging Assessments

S Rohekar, T Boyd, R Lambert, M Beaton, N Chande, J Gregor, H Lennox, K McIntosh, T Ponich, A Rahman, T Sharma, M Sey, M Tauqir, V Jairath
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Abstract

Background Prior case series indicated a temporal relationship between use of vedolizumab and new-onset spondyloarthritis. Methods We aimed to evaluate the relationship between initiation of vedolizumab and development of new-onset spondyloarthritis in patients with inflammatory bowel disease, through serial clinical evaluation and magnetic resonance imaging. A single-centre prospective observational study of 24 patients with inflammatory bowel disease. Patients were eligible if they had active ulcerative colitis or Crohn’s disease and initiating vedolizumab, had no prior history of arthritis or spondyloarthritis and suitable for undergoing serial magnetic resonance imaging. Clinical evaluation was performed by a rheumatologist prior to first dose of vedolizumab and at weeks 8 and 24 weeks after administration. Axial magnetic resonance imaging was performed at baseline, weeks 8 and 24 and evaluated by a blinded central reader. Results Nine tumour necrosis factor inhibitor-naïve patients (4 male; mean age 53.2 yrs; 6 ulcerative colitis; 3 Crohn’s disease) and eight tumour necrosis factor inhibitor-experienced patients (7 male; mean age 48 yrs; 3 ulcerative colitis; 5 Crohn’s disease) completed all assessments. No patients developed new features of axial arthritis either on clinical or blinded radiological assessment at weeks 8 or 24, nor any features of peripheral spondyloarthritis including inflammatory oligoarthritis, enthesitis, dactylitis, or psoriasis (nail, body, or scalp). Both the tumour necrosis factor inhibitor-naive and tumour necrosis factor inhibitor-experienced patients demonstrated good intestinal response to vedolizumab. Conclusion Initiation of vedolizumab did not induce new features of axial or peripheral spondyloarthritis in tumour necrosis factor inhibitor-experienced or tumour necrosis factor inhibitor-naive patients with inflammatory bowel disease.
P696 炎症性肠病患者开始使用维多珠单抗不会引发新发脊柱关节炎:一项包括风湿病学和盲法成像评估的前瞻性研究
背景 之前的系列病例表明,使用维多珠单抗与新发脊柱关节炎之间存在时间关系。方法 我们旨在通过系列临床评估和磁共振成像,评估炎症性肠病患者开始使用维多珠单抗与新发脊柱关节炎之间的关系。这是一项针对 24 名炎症性肠病患者的单中心前瞻性观察研究。如果患者患有活动性溃疡性结肠炎或克罗恩病并开始使用维多珠单抗,既往无关节炎或脊柱关节炎病史,且适合接受序列磁共振成像检查,则符合研究条件。在首次服用维多珠单抗之前以及用药后第 8 周和第 24 周,由风湿免疫科医生进行临床评估。在基线、第8周和第24周进行轴向磁共振成像,并由盲人中心阅读器进行评估。结果 9 名肿瘤坏死因子抑制剂无效患者(4 名男性;平均年龄 53.2 岁;6 名溃疡性结肠炎患者;3 名克罗恩病患者)和 8 名肿瘤坏死因子抑制剂有效患者(7 名男性;平均年龄 48 岁;3 名溃疡性结肠炎患者;5 名克罗恩病患者)完成了所有评估。在第 8 周或第 24 周的临床或盲法放射学评估中,没有患者出现新的轴关节炎特征,也没有出现任何外周脊柱关节炎特征,包括炎性少关节炎、腱鞘炎、趾关节炎或银屑病(指甲、身体或头皮)。对肿瘤坏死因子抑制剂无免疫反应的患者和对肿瘤坏死因子抑制剂有免疫反应的患者均对韦多珠单抗表现出良好的肠道反应。结论 有肿瘤坏死因子抑制剂治疗经验的炎症性肠病患者和无肿瘤坏死因子抑制剂治疗经验的炎症性肠病患者开始使用维多珠单抗不会诱发轴性或周围脊柱关节炎的新特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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