Sandy Vien, Elvis Jovanie Arteaga, Sirisha Grandhe, Nuen Tsang Yang, Eric J Mao
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Chi-square tests (or Fisher's exact test) and 2-sample <i>t</i>-tests (or Wilcoxon's rank-sum test) were used to compare categorical and numeric variables between groups, respectively; analyses were performed using R Computing Software versions 3.6.1.</p><p><strong>Results: </strong>Eighty-four patients with ileum-dominant CD and 27 patients with colonic CD were treated with ustekinumab. The median time to follow-up endoscopy was 13 months. Follow-up colonoscopy after ustekinumab therapy was ulcer-free in 45% of ileum-dominant CD and 76% of colonic CD (<i>P</i> = .02). Of patients with ulcers prior to starting ustekinumab, 24% of ileum-dominant CD and 67% of colonic CD were ulcer-free (<i>P</i> = .01). There were similar rates of hospitalizations and surgery and no significant differences in mean calprotectin and CRP between the two groups on follow-up after ustekinumab therapy.</p><p><strong>Conclusions: </strong>This real-world experience of ustekinumab demonstrates higher rates of endoscopic healing among colonic CD when compared to ileum-dominant CD. Disease location may predict endoscopic healing by ustekinumab. Further studies are necessary to expand our understanding of ustekinumab responsiveness to different CD phenotypes.</p>","PeriodicalId":10847,"journal":{"name":"Crohn's & Colitis 360","volume":"6 4","pages":"otae059"},"PeriodicalIF":1.8000,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586627/pdf/","citationCount":"0","resultStr":"{\"title\":\"Real-World Ustekinumab Experience in Ileum-Dominant Versus Colonic Crohn's Disease.\",\"authors\":\"Sandy Vien, Elvis Jovanie Arteaga, Sirisha Grandhe, Nuen Tsang Yang, Eric J Mao\",\"doi\":\"10.1093/crocol/otae059\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Crohn's disease (CD) presents with diverse phenotypes. It remains unclear if CD location affects therapy efficacy. The aim of this study was to compare the real-world performance of ustekinumab in ileum-dominant and colonic CD.</p><p><strong>Methods: </strong>We performed a single-center, IRB-approved, retrospective review of all adult CD patients who received ustekinumab. We stratified patients by ileal involvement: ileum-dominant (ileal and ileocolonic) and colonic CD. The primary outcome was the absence of ulcers on follow-up colonoscopy. The secondary outcomes included CRP, calprotectin, surgery, and hospitalization. Chi-square tests (or Fisher's exact test) and 2-sample <i>t</i>-tests (or Wilcoxon's rank-sum test) were used to compare categorical and numeric variables between groups, respectively; analyses were performed using R Computing Software versions 3.6.1.</p><p><strong>Results: </strong>Eighty-four patients with ileum-dominant CD and 27 patients with colonic CD were treated with ustekinumab. The median time to follow-up endoscopy was 13 months. Follow-up colonoscopy after ustekinumab therapy was ulcer-free in 45% of ileum-dominant CD and 76% of colonic CD (<i>P</i> = .02). Of patients with ulcers prior to starting ustekinumab, 24% of ileum-dominant CD and 67% of colonic CD were ulcer-free (<i>P</i> = .01). There were similar rates of hospitalizations and surgery and no significant differences in mean calprotectin and CRP between the two groups on follow-up after ustekinumab therapy.</p><p><strong>Conclusions: </strong>This real-world experience of ustekinumab demonstrates higher rates of endoscopic healing among colonic CD when compared to ileum-dominant CD. Disease location may predict endoscopic healing by ustekinumab. 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引用次数: 0
摘要
背景:克罗恩病(CD)表现出多种表型。目前尚不清楚克罗恩病的部位是否会影响疗效。本研究旨在比较乌司替尼在回肠为主型和结肠型 CD 中的实际疗效:我们对所有接受过乌司替尼治疗的成年 CD 患者进行了单中心、经 IRB 批准的回顾性研究。我们根据回肠受累情况对患者进行了分层:回肠主导型(回肠和回结肠)和结肠 CD。主要结果是随访结肠镜检查未发现溃疡。次要结果包括 CRP、钙蛋白、手术和住院。采用卡方检验(或费雪精确检验)和双样本t检验(或Wilcoxon秩和检验)分别比较组间的分类变量和数字变量;分析使用R计算软件3.6.1版进行:84名回肠型CD患者和27名结肠型CD患者接受了乌司替尼治疗。随访内镜检查的中位时间为 13 个月。45%的回肠型CD患者和76%的结肠型CD患者在接受乌司替尼治疗后的随访结肠镜检查中没有发现溃疡(P = .02)。在开始使用乌司替库单抗前有溃疡的患者中,24% 的回肠主导型 CD 和 67% 的结肠型 CD 无溃疡(P = .01)。两组患者的住院率和手术率相似,两组患者在接受乌司替库单抗治疗后的随访中,平均钙蛋白和CRP没有明显差异:结论:乌斯特库单抗的实际应用表明,与回肠为主的CD相比,结肠型CD的内镜愈合率更高。疾病位置可能预示着乌司替库单抗的内镜下愈合率。有必要开展进一步研究,以加深我们对乌司替库单抗对不同CD表型的反应性的了解。
Real-World Ustekinumab Experience in Ileum-Dominant Versus Colonic Crohn's Disease.
Background: Crohn's disease (CD) presents with diverse phenotypes. It remains unclear if CD location affects therapy efficacy. The aim of this study was to compare the real-world performance of ustekinumab in ileum-dominant and colonic CD.
Methods: We performed a single-center, IRB-approved, retrospective review of all adult CD patients who received ustekinumab. We stratified patients by ileal involvement: ileum-dominant (ileal and ileocolonic) and colonic CD. The primary outcome was the absence of ulcers on follow-up colonoscopy. The secondary outcomes included CRP, calprotectin, surgery, and hospitalization. Chi-square tests (or Fisher's exact test) and 2-sample t-tests (or Wilcoxon's rank-sum test) were used to compare categorical and numeric variables between groups, respectively; analyses were performed using R Computing Software versions 3.6.1.
Results: Eighty-four patients with ileum-dominant CD and 27 patients with colonic CD were treated with ustekinumab. The median time to follow-up endoscopy was 13 months. Follow-up colonoscopy after ustekinumab therapy was ulcer-free in 45% of ileum-dominant CD and 76% of colonic CD (P = .02). Of patients with ulcers prior to starting ustekinumab, 24% of ileum-dominant CD and 67% of colonic CD were ulcer-free (P = .01). There were similar rates of hospitalizations and surgery and no significant differences in mean calprotectin and CRP between the two groups on follow-up after ustekinumab therapy.
Conclusions: This real-world experience of ustekinumab demonstrates higher rates of endoscopic healing among colonic CD when compared to ileum-dominant CD. Disease location may predict endoscopic healing by ustekinumab. Further studies are necessary to expand our understanding of ustekinumab responsiveness to different CD phenotypes.