炎症性肠病中二线和三线生物制剂的持久性:一项多中心队列研究

T. Hanrahan, R. Chan, D. Tassone, N. Ding, C. Basnayake, J. Schulberg, A. Vasudevan, M. Kamm, M. De Gregorio, D. V. van Langenberg, O. Niewiadomski
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摘要

背景:尽管已证实生物制剂对炎症性肠病(IBD)有效,但许多生物制剂表现出原发性无反应或继发性反应丧失,并转而使用后续生物制剂。在这里,我们在现实世界的患者队列中确定了IBD的二线和/或三线生物学持久性的早期预测因素。方法:一项回顾性多中心队列研究对2005-2021年接受二线和/或三线生物制剂治疗IBD的患者进行了研究。应用Cox回归来确定治疗失败前更长的累积生物学持久性的预测因素。结果:179例接受≥2种生物制剂治疗的患者中,159例(88.8%)接受了一线抗肿瘤坏死因子(anti-TNF)治疗。首先接受抗肿瘤坏死因子治疗的患者与首先接受非抗肿瘤坏死因子治疗的患者相比,治疗持续时间较长的可能性显著增加(p < 0.01)。诊断为CD (OR 7.1, 95% CI [2.3-21.7], p < 0.01)和内镜下首次生物治疗缓解(OR 10.4 [1.3-79.9], p = 0.03)是生物治疗持续时间较长的积极预测因素,而IBD诊断时年龄越大(OR 0.97 [0.94-0.99], p = 0.04)和最初生物治疗无反应(OR 0.3 [0.1-0.7], p < 0.01)与生物治疗持续时间呈负相关。结论:这些真实世界的数据证明了多种简单识别的因素,这些因素提供了早期客观评估一线生物药物反应的潜力,以预测未来的生物持久性。
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Persistence of Second and Third-Line Biologics in Inflammatory Bowel Disease: A Multi-Centre Cohort Study
Background: Despite proven efficacy of biologics in inflammatory bowel disease (IBD), many exhibit primary non-response or secondary loss of response and switch to subsequent biologic(s). Here, we identified early predictors of second- and/or third-line biologic persistence in IBD, in a real-world cohort of patients. Methods: A retrospective multicentre cohort study was conducted on patients receiving second- and/or third-line biologics for IBD from 2005–2021. Cox regression was applied to identify factors predictive of longer cumulative biologic persistence prior to treatment failure. Results: Of 179 patients who received ≥2 biologics, 159 (88.8%) received an anti-tumour necrosis factor (anti-TNF) first-line. There was a significantly increased likelihood of longer treatment persistence in recipients who received an anti-TNF first, versus those that received a non-anti-TNF agent first (p < 0.01). A diagnosis of CD (OR 7.1, 95% CI [2.3–21.7], p < 0.01), and endoscopic remission achieved on the first biologic (OR 10.4 [1.3–79.9], p = 0.03) were positive predictors of longer biologic persistence, whilst advancing age at IBD diagnosis (OR 0.97 [0.94–0.99], p = 0.04) and primary non-response to initial biologic (OR 0.3 [0.1–0.7], p < 0.01) were inversely associated with biologic persistence. Conclusions: These real-world data demonstrate multiple, simple to identify factors that offer the potential for early objectively assessed response to first-line biologic to predict future biologic persistence.
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