Zhuleku Evi, Wirth Daniel, Nissinen Riikka, Bravatà Ivana, Ziavra Despina, Duva Andreas, Lee Jennifer, Fuchs Andreas, Mueller Sabrina, Wilke Thomas, Bokemeyer Bernd
Cytel Inc., Potsdamer Str. 58, Berlin 10785, Germany.
Janssen-Cilag GmbH, Neuss, Germany.
Therap Adv Gastroenterol. 2024 Jul 30;17:17562848241262288. doi: 10.1177/17562848241262288. eCollection 2024.
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.
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.
Retrospective cohort study in Germany.
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).
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, = 0.012], and switch a second time (HR, 3.46, 95% CI, 1.89-6.36, < 0.001). Moreover, WCS showed an increased likelihood of initiating prolonged corticosteroid therapy (HR, 1.42, 95% CI, 0.77-2.59, = 0.260); however, the results were not significant.
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.
生物制剂已被证明在治疗溃疡性结肠炎(UC)方面有效;然而,在现实世界中,肿瘤坏死因子抑制剂(TNFi)治疗失败很常见。关于治疗失败后临床实践中优先序贯治疗的数据仍然有限。
本研究旨在评估在一线使用TNFi治疗失败后,循环使用TNFi或改用非TNFi生物制剂的患者的真实世界结局。
德国的一项回顾性队列研究。
利用法定疾病基金提供的2014年5月1日至2022年6月30日的行政索赔数据识别成年UC患者。识别出首次开始使用TNFi一线治疗然后改用另一种药物的患者。如果患者循环使用另一种TNFi,则定义为同类转换(WCS);如果他们改用非TNFi生物制剂[乌司奴单抗(UST)或维多珠单抗(VDZ)],则定义为异类转换者(OCS),并从索引(转换日期)开始随访至死亡、保险终止或2022年6月30日的研究结束。进行治疗权重逆概率(IPTW)以调整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)和次要结局(无皮质类固醇药物生存期)。
我们识别出166例开始使用TNFi并改用后续治疗的患者(平均年龄:42.9岁,49.4%为女性)。经过IPTW后,WCS组和OCS组分别有71例和76例患者。与OCS相比,WCS更有可能停用新疗法[风险比(HR),1.82,95%置信区间(CI),1.14 - 2.89,P = 0.012],并且更有可能再次转换治疗(HR,3.46,95% CI,1.89 - 6.36,P < 0.001)。此外,WCS开始长期使用皮质类固醇治疗的可能性增加(HR,1.42,95% CI,0.77 - 2.59,P = 0.260);然而,结果并不显著。
本研究表明,在一线TNFi治疗失败后,与改用UST或VDZ等非TNFi生物制剂相比,UC患者循环使用另一种TNFi的真实世界结局较差。