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瑞士炎症性肠病队列中肿瘤坏死因子拮抗剂随时间的转换及相关危险因素分析。

Analysis of TNF-antagonist switch over time and associated risk factors in the Swiss Inflammatory Bowel Disease Cohort.

作者信息

Hiroz Philippe, Vavricka Stephan R, Fournier Nicolas, Safroneeva Ekaterina, Pittet Valérie, Rogler Gerhard, Schoepfer Alain M

机构信息

Division of Gastroenterology and Hepatology, Centre Hospitalier Universitaire Vaudois , Lausanne , Switzerland.

出版信息

Scand J Gastroenterol. 2014 Oct;49(10):1207-18. doi: 10.3109/00365521.2014.946082. Epub 2014 Aug 14.

Abstract

BACKGROUND AND AIMS

Limited data from large cohorts are available on tumor necrosis factor (TNF) antagonists (infliximab, adalimumab, certolizumab pegol) switch over time. We aimed to evaluate the prevalence of switching from one TNF antagonist to another and to identify associated risk factors.

METHODS

Data from the Swiss Inflammatory Bowel Diseases Cohort Study (SIBDCS) were analyzed.

RESULTS

Of 1731 patients included into the SIBDCS (956 with Crohn's disease [CD] and 775 with ulcerative colitis [UC]), 347 CD patients (36.3%) and 129 UC patients (16.6%) were treated with at least one TNF antagonist. A total of 53/347 (15.3%) CD patients (median disease duration 9 years) and 20/129 (15.5%) of UC patients (median disease duration 7 years) needed to switch to a second and/or a third TNF antagonist, respectively. Median treatment duration was longest for the first TNF antagonist used (CD 25 months; UC 14 months), followed by the second (CD 13 months; UC 4 months) and third TNF antagonist (CD 11 months; UC 15 months). Primary nonresponse, loss of response and side effects were the major reasons to stop and/or switch TNF antagonist therapy. A low body mass index, a short diagnostic delay and extraintestinal manifestations at inclusion were identified as risk factors for a switch of the first used TNF antagonist within 24 months of its use in CD patients.

CONCLUSION

Switching of the TNF antagonist over time is a common issue. The median treatment duration with a specific TNF antagonist is diminishing with an increasing number of TNF antagonists being used.

摘要

背景与目的

关于肿瘤坏死因子(TNF)拮抗剂(英夫利昔单抗、阿达木单抗、赛妥珠单抗)随时间转换的数据,来自大型队列研究的资料有限。我们旨在评估从一种TNF拮抗剂转换为另一种的发生率,并确定相关危险因素。

方法

分析瑞士炎症性肠病队列研究(SIBDCS)的数据。

结果

纳入SIBDCS的1731例患者中(956例克罗恩病[CD]患者和775例溃疡性结肠炎[UC]患者),347例CD患者(36.3%)和129例UC患者(16.6%)接受了至少一种TNF拮抗剂治疗。分别有53/347(15.3%)例CD患者(疾病中位病程9年)和20/129(15.5%)例UC患者(疾病中位病程7年)需要转换为第二种和/或第三种TNF拮抗剂。使用的第一种TNF拮抗剂治疗中位持续时间最长(CD为25个月;UC为14个月),其次是第二种(CD为13个月;UC为4个月)和第三种TNF拮抗剂(CD为11个月;UC为15个月)。原发性无反应、反应丧失和副作用是停止和/或转换TNF拮抗剂治疗的主要原因。低体重指数、诊断延迟短以及纳入时的肠外表现被确定为CD患者在首次使用TNF拮抗剂24个月内转换的危险因素。

结论

TNF拮抗剂随时间转换是一个常见问题。随着使用的TNF拮抗剂数量增加,特定TNF拮抗剂的治疗中位持续时间在缩短。

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