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与抗肿瘤坏死因子预防克罗恩病术后复发疗效相关的因素。

Factors associated with anti-tumor necrosis factor effectiveness to prevent postoperative recurrence in Crohn's disease.

作者信息

Buisson Anthony, Cannon Lisa, Umanskiy Konstantin, Hurst Roger D, Hyman Neil H, Sakuraba Atsushi, Pekow Joel, Dalal Sushila, Cohen Russell D, Pereira Bruno, Rubin David T

机构信息

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, IL, USA.

Inflammatory Bowel Unit, Inserm, 3iHP, CHU Clermont-Ferrand, Clermont Auvergne University, Clermont-Ferrand, France.

出版信息

Intest Res. 2022 Jul;20(3):303-312. doi: 10.5217/ir.2021.00018. Epub 2021 Aug 4.

DOI:10.5217/ir.2021.00018
PMID:34333909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9344250/
Abstract

BACKGROUND/AIMS: We assessed the effectiveness of anti-TNF agents and its associated factors to prevent endoscopic and clinical postoperative recurrence (POR) in Crohn's disease (CD).

METHODS

From a prospectively-maintained database, we retrieved 316 CD patients who underwent intestinal resection (2011-2017). Endoscopic (Rutgeerts index ≥ i2 at 6 months) and clinical (recurrence of symptoms leading to hospitalization or therapeutic escalation) POR were assessed.

RESULTS

In 117 anti-TNF-naïve patients, anti-TNF therapy was more effective than immunosuppressive agents (odds ratio [OR], 8.8; 95% confidence interval [CI], 1.8-43.9; P= 0.008) and no medication/5-aminosalicylates (OR, 5.2; 95% CI, 1.0-27.9; P= 0.05) to prevent endoscopic POR. In 199 patients exposed to anti-TNF prior to the surgery, combination with anti-TNF and immunosuppressive agents was more effective than anti-TNF monotherapy (OR, 2.32; 95% CI, 1.02-5.31; P= 0.046) to prevent endoscopic POR. Primary failure to anti-TNF agent prior to surgery was predictive of anti-TNF failure to prevent endoscopic POR (OR, 2.41; 95% CI, 1.10-5.32; P= 0.03). When endoscopic POR despite anti-TNF prophylactic medication (n = 55), optimizing anti-TNF and adding an immunosuppressive drug was the most effective option to prevent clinical POR (hazard ratio, 7.38; 95% CI, 1.54-35.30; P= 0.012). Anti-TNF therapy was the best option to prevent clinical POR (hazard ratio, 3.10; 95% CI, 1.09-8.83; P= 0.034) in patients with endoscopic POR who did not receive any biologic to prevent endoscopic POR (n = 55).

CONCLUSIONS

Anti-TNF was the most effective medication to prevent endoscopic and clinical POR. Combination with anti-TNF and immunosuppressive agents should be considered in patients previously exposed to anti-TNF.

摘要

背景/目的:我们评估了抗TNF药物预防克罗恩病(CD)内镜及临床术后复发(POR)的有效性及其相关因素。

方法

从一个前瞻性维护的数据库中,我们检索了316例接受肠道切除术的CD患者(2011 - 2017年)。评估内镜下(6个月时鲁氏分级指数≥i2)及临床(因症状复发导致住院或治疗升级)POR情况。

结果

在117例未使用过抗TNF药物的患者中,抗TNF治疗在预防内镜下POR方面比免疫抑制剂(优势比[OR],8.8;95%置信区间[CI],1.8 - 43.9;P = 0.008)和未用药/5 - 氨基水杨酸类药物(OR,5.2;95% CI,1.0 - 27.9;P = 0.05)更有效。在199例手术前已接触过抗TNF药物的患者中,抗TNF与免疫抑制剂联合使用在预防内镜下POR方面比抗TNF单药治疗更有效(OR,2.32;95% CI,1.02 - 5.31;P = 0.046)。手术前抗TNF药物原发性失效可预测抗TNF预防内镜下POR失败(OR,2.41;95% CI,1.10 - 5.32;P = 0.03)。当尽管使用抗TNF预防性药物仍发生内镜下POR时(n = 55),优化抗TNF并加用免疫抑制药物是预防临床POR的最有效选择(风险比,7.38;95% CI,1.54 - 35.30;P = 0.012)。在未接受任何生物制剂预防内镜下POR的内镜下POR患者中(n = 55),抗TNF治疗是预防临床POR的最佳选择(风险比,3.10;95% CI,1.09 - 8.83;P = 0.034)。

结论

抗TNF是预防内镜及临床POR最有效的药物。对于既往接触过抗TNF的患者,应考虑抗TNF与免疫抑制剂联合使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/339d6beec3a5/ir-2021-00018f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/4850fde79ac2/ir-2021-00018f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/595fb7d44f24/ir-2021-00018f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/f40076693e53/ir-2021-00018f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/debc28f79d60/ir-2021-00018f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/339d6beec3a5/ir-2021-00018f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/4850fde79ac2/ir-2021-00018f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/595fb7d44f24/ir-2021-00018f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/f40076693e53/ir-2021-00018f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/debc28f79d60/ir-2021-00018f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ad/9344250/339d6beec3a5/ir-2021-00018f5.jpg

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