溃疡性结肠炎患者一线 TNFi 治疗失败后的类内转换与类外转换:来自德国索赔数据分析的实际结果。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-07-30 eCollection Date: 2024-01-01 DOI:10.1177/17562848241262288
Evi Zhuleku, Daniel Wirth, Riikka Nissinen, Ivana Bravatà, Despina Ziavra, Andreas Duva, Jennifer Lee, Andreas Fuchs, Sabrina Mueller, Thomas Wilke, Bernd Bokemeyer
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引用次数: 0

摘要

背景:生物制剂在治疗溃疡性结肠炎(UC)方面疗效显著;但在现实世界中,肿瘤坏死因子抑制剂(TNFi)治疗失败的情况很常见。有关治疗失败后临床实践中优先排序的数据仍然有限:本研究旨在评估一线TNFis治疗失败后,患者循环使用TNFis或转用非TNFi生物制剂的实际疗效:设计:德国的回顾性队列研究:通过法定疾病基金提供的2014年5月1日至2022年6月30日的行政报销数据,确定UC成人患者。对新近开始接受 TNFis 一线治疗后转用其他药物的患者进行了识别。如果患者循环使用另一种TNFi,则被定义为类内转换患者(WCS);如果患者转换使用非TNFi生物制剂[乌司替尼(UST)或维妥珠单抗(VDZ)],则被定义为类外转换患者(OCS),并从指数(转换日期)到2022年6月30日死亡、保险结束或研究结束进行随访。采用治疗反概率加权法(IPTW)调整各组间基线特征的差异,并使用加权Cox回归模型比较主要结局(停药时间和第二次治疗转换时间)和次要结局(无皮质类固醇药物生存期):我们确定了166名开始接受TNFis治疗并转为后续治疗的患者(平均年龄:42.9岁,49.4%为女性)。IPTW治疗后,WCS组和OCS组分别有71名和76名患者。与OCS相比,WCS更有可能停止新疗法[危险比(HR),1.82,95%置信区间(CI),1.14-2.89,P = 0.012],并更有可能第二次转用新疗法(HR,3.46,95% CI,1.89-6.36,P = 0.260);但结果并不显著:结论:本研究表明,UC患者在一线TNFi治疗失败后,与改用UST或VDZ等非TNFi治疗相比,改用另一种TNFi治疗的实际疗效较差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Switching within versus out of class following first-line TNFi failure in ulcerative colitis: real-world outcomes from a German claims data analysis.

Background: Biologic agents have demonstrated efficacy in treating ulcerative colitis (UC); however, treatment failure to tumor necrosis factor inhibitors (TNFi) is common in the real world. Data on preferential sequencing in clinical practice after failure remain limited.

Objectives: This study aimed to evaluate real-world outcomes of patients cycling to TNFis or switching to non-TNFi biologics following first-line failure with TNFis.

Design: Retrospective cohort study in Germany.

Methods: Adult patients with UC were identified using administrative claims data from 1 May 2014 to 30 June 2022 provided by a statutory sickness fund. Patients newly initiating first-line therapy with TNFis and then switching to another agent were identified. Patients were defined as within-class switched (WCS), if they cycled to another TNFi, or outside-class switchers (OCS), if they switched to a non-TNFi biologic [ustekinumab (UST) or vedolizumab (VDZ)] and followed from index (switch date) to death, insurance end, or study end on 30 June 2022. Inverse probability of treatment weighting (IPTW) was performed to adjust for differences in baseline characteristics between groups, and weighted Cox regression models were used to compare primary (time to discontinuation and second treatment switch) and secondary outcomes (corticosteroid-free drug survival).

Results: We identified 166 patients initiating TNFis and switching to a subsequent treatment (mean age: 42.9 years, 49.4% female). Following IPTW, there were 71 and 76 patients in the WCS and OCS groups, respectively. Compared to OCS, WCS were more likely to discontinue the new therapy [hazard ratio (HR), 1.82, 95% confidence interval (CI), 1.14-2.89, p = 0.012], and switch a second time (HR, 3.46, 95% CI, 1.89-6.36, p < 0.001). Moreover, WCS showed an increased likelihood of initiating prolonged corticosteroid therapy (HR, 1.42, 95% CI, 0.77-2.59, p = 0.260); however, the results were not significant.

Conclusion: Following first-line TNFi failure, this study suggests that real-world outcomes among patients with UC are less favorable when cycling to another TNFi, compared to switching to a non-TNFi such as UST or VDZ.

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