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基于临床与基于血药浓度的英夫利昔单抗给药治疗炎症性肠病患者的黏膜愈合和长期结局比较。

Mucosal Healing and Long-term Outcomes of Patients With Inflammatory Bowel Diseases Receiving Clinic-Based vs Trough Concentration-Based Dosing of Infliximab.

机构信息

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.

Department of Pharmaceutical and Pharmacological Sciences, Laboratory for Therapeutic and Diagnostic Antibodies, KU Leuven, Leuven, Belgium; Department of Medicine, University of California San Diego, La Jolla, California.

出版信息

Clin Gastroenterol Hepatol. 2018 Aug;16(8):1276-1283.e1. doi: 10.1016/j.cgh.2017.11.046. Epub 2017 Dec 1.

Abstract

BACKGROUND & AIMS: The Trough Concentration Adapted Infliximab Treatment (TAXIT) trial demonstrated that maintaining infliximab trough concentrations at 3 to 7 μg/mL is most effective at inducing remission in patients with inflammatory bowel diseases (IBDs), with fewer flares than clinic-based dosing. We performed a follow-up analysis of study participants to explore the correlation between trough dosing strategy and mucosal healing, continued infliximab use, and rates of hospitalization, surgery, and steroid use.

METHODS

This was a retrospective single-center study of 226 patients with IBD who completed the maintenance phase of TAXIT, performed at the University Hospitals of Leuven in Belgium. Baseline patient characteristics, laboratory test results, and endoscopic data were obtained at the end of that study between June 2012 and December 2013 (n = 125). Long-term outcome data (IBD-related hospitalization, abdominal surgery, and systemic steroid use) were collected from the time of the last TAXIT study visit (August 2012-April 2013) until April 1, 2016. We also collected data on continued use of infliximab and trough concentrations.

RESULTS

At baseline, 91% of patients in the clinic-based dosing group and 90% of patients in the trough concentration-based dosing group had mucosal healing. After a median follow-up time of 41 months (interquartile range, 39-42 mo), infliximab treatment was continued by 81 of 108 patients (75%) from the clinic-based dosing group and 86 of 107 (80%) from the trough concentration-based dosing group. However, within 1 year, infliximab was discontinued by 10 of 27 patients (37%) from the clinic-based dosing group and 2 of 21 patients (10%) from the trough concentration-based dosing group (P = .04). The rates of hospitalization, surgery, and steroid use were below 15% in both groups.

CONCLUSIONS

At the end of a trial of clinic-based dosing vs trough concentration-based dosing of infliximab in patients with IBD, most patients had mucosal healing. Most patients (≥75%) in both groups continued taking infliximab for more than 3 years after the trial, but a significantly higher proportion of patients in the clinic-based dosing group discontinued infliximab in the first year after the end of the trial. Both groups had low rates of hospitalization, surgery, and steroid use.

摘要

背景与目的

Trough Concentration Adapted Infliximab Treatment(TAXIT)试验表明,维持英夫利昔单抗的谷浓度在 3 至 7μg/mL 之间,最能有效诱导炎症性肠病(IBD)患者缓解,其缓解发作率低于基于临床的剂量。我们对研究参与者进行了随访分析,以探讨谷浓度策略与黏膜愈合、持续使用英夫利昔单抗以及住院、手术和使用类固醇的发生率之间的相关性。

方法

这是一项在比利时鲁汶大学医院进行的回顾性单中心研究,共纳入 226 例完成 TAXIT 维持期的 IBD 患者。在该研究结束时(2012 年 6 月至 2013 年 12 月)获得了基线患者特征、实验室检查结果和内镜数据(n=125)。从 TAXIT 研究的最后一次就诊时间(2012 年 8 月至 2013 年 4 月)到 2016 年 4 月 1 日,收集了长期结局数据(与 IBD 相关的住院、腹部手术和全身类固醇使用)。我们还收集了关于继续使用英夫利昔单抗和谷浓度的数据。

结果

在基于临床的剂量组中,91%的患者和基于谷浓度的剂量组中,90%的患者在基线时具有黏膜愈合。在中位数为 41 个月(四分位距,39-42 个月)的随访后,继续使用英夫利昔单抗的患者分别为 108 例中的 81 例(75%)和 107 例中的 86 例(80%)。然而,在 1 年内,基于临床的剂量组中有 10 例(37%)和基于谷浓度的剂量组中有 2 例(10%)患者停用英夫利昔单抗(P=0.04)。两组的住院、手术和使用类固醇的比例均低于 15%。

结论

在炎症性肠病患者中,英夫利昔单抗基于临床剂量与基于谷浓度剂量的试验结束时,大多数患者具有黏膜愈合。在试验结束后,两组中大多数患者(≥75%)继续使用英夫利昔单抗超过 3 年,但基于临床剂量组的患者在试验结束后的第一年有更高比例停用英夫利昔单抗。两组的住院、手术和使用类固醇的比例均较低。

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