Samuel Raimundo Fernandes, Inês Coelho Rodrigues, André Da Silva Neves, Sofia Saraiva, Ana Rita Gonçalves, Paula Moura Santos, Ana Valente, Luís Araújo Correia, Helena Cortez- Pinto, Fernando Magro
{"title":"早期自上而下的生物制剂治疗可提高克罗恩病经壁缓解率——风险调整倾向评分匹配分析","authors":"Samuel Raimundo Fernandes, Inês Coelho Rodrigues, André Da Silva Neves, Sofia Saraiva, Ana Rita Gonçalves, Paula Moura Santos, Ana Valente, Luís Araújo Correia, Helena Cortez- Pinto, Fernando Magro","doi":"10.1093/ibd/izaf112","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Early top-down treatment with biologics has been associated with higher rates of endoscopic remission compared to step-up treatment in Crohn's disease (CD). The benefits in relation to transmural remission are currently unknown. Better stratification of patients suitable for top-down strategies is needed.</p><p><strong>Methods: </strong>Retrospective study including CD patients naïve to immunomodulators and biologics and with endoscopic and radiologic evidence of active disease at baseline. Transmural remission rates were compared between patients receiving early top-down treatment (start of biologics within 6 months of immunomodulators) and conventional step-up treatment (start of biologics > 6 months after immunomodulators). The influence of risk factors for disabling disease (age at diagnosis, disease duration, smoking, phenotype, perianal disease, extensive small bowel disease, and elevated C-reactive protein) on transmural remission rates was also assessed and adjusted through propensity score-matched analysis.</p><p><strong>Results: </strong>In total, 327 patients were included in the main analysis, 47.7% receiving early top-down treatment with biologics. Transmural remission rates decreased from 33.3% to 0% in patients with 0 and 6 risk factors for disabling disease, respectively. Early top-down treatment resulted in higher rates of transmural remission (33.3% vs 18.1%, P = .002) and was an independent predictor for this outcome in the multivariate analysis (odds ratio [OR] 2.187, 95% confidence interval [95% CI], 1.270-3.665, P = .005). Comparable results were found in the propensity score matched analysis (34% vs 17%, P = .002; OR 2.3, 95% CI, 1.268-4.174, P = .006).</p><p><strong>Conclusions: </strong>Early top-down treatment with biologics improves the rates of transmural remission in CD. 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The influence of risk factors for disabling disease (age at diagnosis, disease duration, smoking, phenotype, perianal disease, extensive small bowel disease, and elevated C-reactive protein) on transmural remission rates was also assessed and adjusted through propensity score-matched analysis.</p><p><strong>Results: </strong>In total, 327 patients were included in the main analysis, 47.7% receiving early top-down treatment with biologics. Transmural remission rates decreased from 33.3% to 0% in patients with 0 and 6 risk factors for disabling disease, respectively. Early top-down treatment resulted in higher rates of transmural remission (33.3% vs 18.1%, P = .002) and was an independent predictor for this outcome in the multivariate analysis (odds ratio [OR] 2.187, 95% confidence interval [95% CI], 1.270-3.665, P = .005). 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引用次数: 0
摘要
背景:与克罗恩病(CD)的逐步治疗相比,早期自上而下的生物制剂治疗与更高的内镜缓解率相关。与跨壁缓解相关的益处目前尚不清楚。需要对适合自上而下策略的患者进行更好的分层。方法:回顾性研究包括CD患者naïve免疫调节剂和生物制剂,并在基线时有内窥镜和放射学证据的活动性疾病。比较接受早期自上而下治疗(在免疫调节剂治疗6个月内开始使用生物制剂)和常规强化治疗(在免疫调节剂治疗6个月后开始使用生物制剂)的患者的全壁缓解率。致残疾病的危险因素(诊断年龄、病程、吸烟、表型、肛周疾病、广泛的小肠疾病和c反应蛋白升高)对经壁缓解率的影响也通过倾向评分匹配分析进行了评估和调整。结果:共有327例患者纳入主分析,其中47.7%的患者接受了早期自上而下的生物制剂治疗。在有0和6个致残危险因素的患者中,经壁缓解率分别从33.3%下降到0%。早期自上而下治疗导致更高的跨壁缓解率(33.3% vs 18.1%, P = 0.002),并且在多变量分析中是该结果的独立预测因子(优势比[OR] 2.187, 95%可信区间[95% CI], 1.270-3.665, P = 0.005)。在倾向评分匹配分析中发现了可比较的结果(34% vs 17%, P = 0.002;或2.3,95% ci, 1.268-4.174, p = 0.006)。结论:早期自上而下的生物制剂治疗提高了CD的跨壁缓解率。致残性疾病的危险因素显著影响获得跨壁缓解的机会,并可能帮助临床医生确定适合更积极治疗策略的患者。
Early Top-Down Treatment With Biologics Improves the Rates of Transmural Remission in Crohn's Disease-A Risk-Adjusted Propensity Score Matched Analysis.
Background: Early top-down treatment with biologics has been associated with higher rates of endoscopic remission compared to step-up treatment in Crohn's disease (CD). The benefits in relation to transmural remission are currently unknown. Better stratification of patients suitable for top-down strategies is needed.
Methods: Retrospective study including CD patients naïve to immunomodulators and biologics and with endoscopic and radiologic evidence of active disease at baseline. Transmural remission rates were compared between patients receiving early top-down treatment (start of biologics within 6 months of immunomodulators) and conventional step-up treatment (start of biologics > 6 months after immunomodulators). The influence of risk factors for disabling disease (age at diagnosis, disease duration, smoking, phenotype, perianal disease, extensive small bowel disease, and elevated C-reactive protein) on transmural remission rates was also assessed and adjusted through propensity score-matched analysis.
Results: In total, 327 patients were included in the main analysis, 47.7% receiving early top-down treatment with biologics. Transmural remission rates decreased from 33.3% to 0% in patients with 0 and 6 risk factors for disabling disease, respectively. Early top-down treatment resulted in higher rates of transmural remission (33.3% vs 18.1%, P = .002) and was an independent predictor for this outcome in the multivariate analysis (odds ratio [OR] 2.187, 95% confidence interval [95% CI], 1.270-3.665, P = .005). Comparable results were found in the propensity score matched analysis (34% vs 17%, P = .002; OR 2.3, 95% CI, 1.268-4.174, P = .006).
Conclusions: Early top-down treatment with biologics improves the rates of transmural remission in CD. Risk factors for disabling disease significantly impact the chances of obtaining transmural remission and may help clinicians identify patients suitable for more aggressive treatment strategies.
期刊介绍:
Inflammatory Bowel Diseases® supports the mission of the Crohn''s & Colitis Foundation by bringing the most impactful and cutting edge clinical topics and research findings related to inflammatory bowel diseases to clinicians and researchers working in IBD and related fields. The Journal is committed to publishing on innovative topics that influence the future of clinical care, treatment, and research.