I Latras-Cortés, J C Sáez Hortelano, P Suárez-Álvarez, N Cano-Sanz, L Ortega-Valin, M Sierra-Ausín
{"title":"抗肿瘤坏死因子失效后Ustekinumab治疗克罗恩病的持久性和疗效:一项观察性研究","authors":"I Latras-Cortés, J C Sáez Hortelano, P Suárez-Álvarez, N Cano-Sanz, L Ortega-Valin, M Sierra-Ausín","doi":"10.1007/s10620-025-08978-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Anti-TNF treatment failure in Crohn's disease is common, and the literature on the selection of subsequent treatment is scant. Ustekinumab may be associated with high persistence rates and it appears to be effective in perianal disease.</p><p><strong>Aims: </strong>Primary objective: persistence, clinical, and biologic remission with ustekinumab.</p><p><strong>Secondary objectives: </strong>Persistence of the first biologic therapy, reasons for change of treatment, need for dose optimization, surgery, hospitalizations, and adverse events with ustekinumab.</p><p><strong>Methods: </strong>Retrospective, observational, single-center study from a prospective database of Crohn's disease adult patients receiving ustekinumab after failure of anti-TNF or vedolizumab. A sub-analysis was performed to evaluate ustekinumab persistence after the approval of risankizumab and upadacitinib.</p><p><strong>Results: </strong>Mean duration with ustekinumab was 27.65 months (SD 18.27) and persistence was 86.76%. Clinical remission was 40.63% at week 4, 54.35% at week 8, 54.9% at year 1, 76.92% at year 4, and 100% at year 5. Persistence with ustekinumab was longer than with anti-TNF: year 1, 93.2 vs 72.06%; year 2, 89.4 vs 45.59%; and year 3, 86.1 vs 30.88%. Just over one-third (36.76%) of patients required dose optimization. Nine (13.24%) patients stopped treatment due to primary non-response [1 (1.47%)], loss of response [5(7.35%)], and adverse events [3 (4.41%)]. Eleven (16.18%) patients needed surgery and hospitalization. After the approval of upadacitinib and risankizumab, ustekinumab persistence was 80.88%. Seven (70%) of the patients with perianal disease achieved clinical remission and 4 (40%) completed fistula healing.</p><p><strong>Conclusions: </strong>Ustekinumab may have better persistence as a second-line treatment compared to anti-TNF and may be effective in perianal disease.</p>","PeriodicalId":11378,"journal":{"name":"Digestive Diseases and Sciences","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Persistence and Efficacy of Ustekinumab in Crohn's Disease After Anti-TNF Failure: An Observational Study.\",\"authors\":\"I Latras-Cortés, J C Sáez Hortelano, P Suárez-Álvarez, N Cano-Sanz, L Ortega-Valin, M Sierra-Ausín\",\"doi\":\"10.1007/s10620-025-08978-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Anti-TNF treatment failure in Crohn's disease is common, and the literature on the selection of subsequent treatment is scant. Ustekinumab may be associated with high persistence rates and it appears to be effective in perianal disease.</p><p><strong>Aims: </strong>Primary objective: persistence, clinical, and biologic remission with ustekinumab.</p><p><strong>Secondary objectives: </strong>Persistence of the first biologic therapy, reasons for change of treatment, need for dose optimization, surgery, hospitalizations, and adverse events with ustekinumab.</p><p><strong>Methods: </strong>Retrospective, observational, single-center study from a prospective database of Crohn's disease adult patients receiving ustekinumab after failure of anti-TNF or vedolizumab. A sub-analysis was performed to evaluate ustekinumab persistence after the approval of risankizumab and upadacitinib.</p><p><strong>Results: </strong>Mean duration with ustekinumab was 27.65 months (SD 18.27) and persistence was 86.76%. Clinical remission was 40.63% at week 4, 54.35% at week 8, 54.9% at year 1, 76.92% at year 4, and 100% at year 5. 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引用次数: 0
摘要
背景:抗肿瘤坏死因子治疗在克罗恩病中失败是常见的,关于后续治疗选择的文献很少。乌斯特金单抗可能与高持续率有关,它似乎对肛周疾病有效。目的:主要目的:ustekinumab的持久性、临床和生物学缓解。次要目标:第一次生物治疗的持续性、改变治疗的原因、剂量优化的需要、手术、住院和ustekinumab的不良事件。方法:回顾性、观察性、单中心研究,来自前瞻性数据库的克罗恩病成年患者在抗肿瘤坏死因子或维多单抗治疗失败后接受ustekinumab治疗。在risankizumab和upadacitinib获批后,进行了一项亚分析来评估ustekinumab的持久性。结果:ustekinumab的平均持续时间为27.65个月(SD 18.27),持续时间为86.76%。第4周临床缓解率为40.63%,第8周为54.35%,第1年为54.9%,第4年为76.92%,第5年为100%。ustekinumab组的持续时间长于抗tnf组:1 93.2年vs 72.06%;第二年:89.4 vs 45.59%;第三年,86.1 vs 30.88%。超过三分之一(36.76%)的患者需要优化剂量。9例(13.24%)患者因原发性无反应[1例(1.47%)]、无反应[5例(7.35%)]、不良事件[3例(4.41%)]而停止治疗。11例(16.18%)患者需要手术和住院治疗。在upadacitinib和risankizumab获批后,ustekinumab的持久性为80.88%。7例(70%)肛周疾病患者达到临床缓解,4例(40%)完成瘘管愈合。结论:与抗肿瘤坏死因子相比,Ustekinumab作为二线治疗可能具有更好的持久性,并且可能对肛周疾病有效。
Persistence and Efficacy of Ustekinumab in Crohn's Disease After Anti-TNF Failure: An Observational Study.
Background: Anti-TNF treatment failure in Crohn's disease is common, and the literature on the selection of subsequent treatment is scant. Ustekinumab may be associated with high persistence rates and it appears to be effective in perianal disease.
Aims: Primary objective: persistence, clinical, and biologic remission with ustekinumab.
Secondary objectives: Persistence of the first biologic therapy, reasons for change of treatment, need for dose optimization, surgery, hospitalizations, and adverse events with ustekinumab.
Methods: Retrospective, observational, single-center study from a prospective database of Crohn's disease adult patients receiving ustekinumab after failure of anti-TNF or vedolizumab. A sub-analysis was performed to evaluate ustekinumab persistence after the approval of risankizumab and upadacitinib.
Results: Mean duration with ustekinumab was 27.65 months (SD 18.27) and persistence was 86.76%. Clinical remission was 40.63% at week 4, 54.35% at week 8, 54.9% at year 1, 76.92% at year 4, and 100% at year 5. Persistence with ustekinumab was longer than with anti-TNF: year 1, 93.2 vs 72.06%; year 2, 89.4 vs 45.59%; and year 3, 86.1 vs 30.88%. Just over one-third (36.76%) of patients required dose optimization. Nine (13.24%) patients stopped treatment due to primary non-response [1 (1.47%)], loss of response [5(7.35%)], and adverse events [3 (4.41%)]. Eleven (16.18%) patients needed surgery and hospitalization. After the approval of upadacitinib and risankizumab, ustekinumab persistence was 80.88%. Seven (70%) of the patients with perianal disease achieved clinical remission and 4 (40%) completed fistula healing.
Conclusions: Ustekinumab may have better persistence as a second-line treatment compared to anti-TNF and may be effective in perianal disease.
期刊介绍:
Digestive Diseases and Sciences publishes high-quality, peer-reviewed, original papers addressing aspects of basic/translational and clinical research in gastroenterology, hepatology, and related fields. This well-illustrated journal features comprehensive coverage of basic pathophysiology, new technological advances, and clinical breakthroughs; insights from prominent academicians and practitioners concerning new scientific developments and practical medical issues; and discussions focusing on the latest changes in local and worldwide social, economic, and governmental policies that affect the delivery of care within the disciplines of gastroenterology and hepatology.