Risankizumab and Certolizumab Pegol Dual-Targeted Therapy for Crohn's Disease and Axial Spondyloarthritis: A Case Report.

IF 0.5 Q4 GASTROENTEROLOGY & HEPATOLOGY
Case Reports in Gastroenterology Pub Date : 2024-12-24 eCollection Date: 2025-01-01 DOI:10.1159/000542759
Anouk Lehmann, Juerg Vosbeck, Diego Kyburz, Petr Hruz, Jan Hendrik Niess
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Abstract

Introduction: Treatment of Crohn's disease (CD) and axial spondyloarthritis (axSpA) is challenging, with CD refractory to anti-TNF antibodies. Here, we present for the first time a case treated with dual-targeted therapy (DTT) using the anti-IL-23 monoclonal risankizumab and the anti-TNF antibody certolizumab pegol.

Case presentation: Our patient initially presented with axSpA at the age of 27. Nine years later, CD was diagnosed by the age of 36. One year after the diagnosis of CD, a spontaneous ileal perforation occurred as part of a disease course refractory to multiple anti-TNF antibodies and intolerance to immunomodulators. However, the axSpA showed a response to the anti-TNF certolizumab pegol. After stopping certolizumab pegol, we enrolled the patient into the M15-991 induction trial (MOTIVATE) and the maintenance trial (FORTIFY) testing the anti-IL-23 antibody risankizumab versus placebo in CD with failure to prior biological therapy. As a result, risankizumab induced a CD response but failed to control the axSpA. Considering the CD refractory and the axSpA responding to anti-TNFs, we initiated a DTT with risankizumab and certolizumab pegol. Risankizumab and certolizumab pegol together improved both CD and axSpA. As adverse events, there were only two episodes of spontaneously resolving common colds during the 19-month reviewed period.

Conclusion: DTT using risankizumab and certolizumab pegol is effective in CD and axSpA without serious adverse events in our patient. Combining biologicals that target specific pathways in immune-mediated diseases promises excellent potential in CD associated with extraintestinal manifestations.

Risankizumab和Certolizumab Pegol双靶向治疗克罗恩病和轴性脊椎关节炎:1例报告。
克罗恩病(CD)和轴性脊柱炎(axSpA)的治疗具有挑战性,CD对抗tnf抗体难治。在这里,我们首次提出了使用抗il -23单克隆risankizumab和抗tnf抗体certolizumab pegol双靶向治疗(DTT)的病例。病例介绍:我们的患者最初在27岁时出现axSpA。9年后,36岁的她被诊断为乳糜泻。在诊断CD一年后,自发性回肠穿孔作为多种抗tnf抗体难治和免疫调节剂不耐受的病程的一部分发生。然而,axSpA对抗tnf的certolizumab pegol有应答。在停止certolizumab pegol后,我们将患者纳入M15-991诱导试验(MOTIVATE)和维持试验(FORTIFY),测试抗il -23抗体risankizumab与安慰剂在既往生物治疗失败的CD中的对比。结果,risankizumab诱导了CD反应,但未能控制axSpA。考虑到CD的难治性和axSpA对抗tnf的反应,我们启动了瑞桑单抗和certolizumab pegol的DTT。Risankizumab和certolizumab pegol共同改善了CD和axSpA。作为不良事件,在19个月的回顾期间,只有两次普通感冒自行消退。结论:我们的患者使用利桑单抗和certolizumab pegol进行DTT治疗CD和axSpA有效,无严重不良事件。结合针对免疫介导疾病中特定途径的生物制剂,有望在与肠外表现相关的乳糜泻中发挥巨大的潜力。
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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来源期刊
Case Reports in Gastroenterology
Case Reports in Gastroenterology Medicine-Gastroenterology
CiteScore
1.10
自引率
0.00%
发文量
99
审稿时长
7 weeks
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