Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Scand J Gastroenterol. 2022 Nov;57(11):1327-1330. doi: 10.1080/00365521.2022.2088248. Epub 2022 Jun 22.
Immunological treatment failure of anti-TNF therapy negatively influences treatment persistence of a second anti-TNF in IBD patients. So far it is unknown if this effect is also observed for other monoclonal antibodies. We assessed the influence of immunogenicity to anti-TNFs on treatment persistence of subsequent ustekinumab and vedolizumab therapy.
IBD patients with and without immunogenicity to anti-TNFs (undetectable trough levels and antibody titers ≥20 ng/mL) and subsequent ustekinumab (UST) and/or vedolizumab (VDZ) therapy were included in this retrospective, single-center study. The Kaplan-Meier method with the log-rank test and Cox proportional hazards were used as statistical methods.
One hundred patients (Crohn's disease: 62, Ulcerative colitis: 31, IBD unclassified: 7) with 127 treatment lines (62 with UST, 65 with VDZ) were included in the analysis. Immunogenicity to previous anti-TNFs did not influence treatment persistence of subsequent ustekinumab and vedolizumab therapy (UST: Log rank: = .95, Immunogenicity: HR for treatment discontinuation: 0.97 [95% CI 0.31-3.04]; VDZ: = .65, HR: 0.85 [0.41-1.75]; total cohort [UST and VDZ]: = .62, HR: 0.86 [0.47-1.57]). Azathioprine co-treatment did not lengthen treatment persistence (UST: Log rank: = .77, azathioprine: HR: 1.20 [0.34-4.27]; VDZ: = .92, HR: 0.58 [0.17-1.99]; total cohort: = .79, HR: 1.10 [0.55-2.20]). In this anti-TNF experienced cohort, patients with ustekinumab remained longer on treatment than patients receiving vedolizumab (Log rank: = .005, UST: HR: 0.43 [0.23-0.79]).
Immunogenicity to anti-TNFs does not influence treatment persistence of subsequent ustekinumab and vedolizumab therapy.
抗 TNF 治疗的免疫治疗失败会对 IBD 患者的第二次抗 TNF 治疗的持续时间产生负面影响。到目前为止,尚不清楚这种影响是否也适用于其他单克隆抗体。我们评估了抗 TNF 药物的免疫原性对后续乌司奴单抗和维得利珠单抗治疗的持续时间的影响。
本回顾性单中心研究纳入了抗 TNF 药物免疫原性(检测不到的谷浓度和抗体滴度≥20ng/ml)和随后乌司奴单抗(UST)和/或维得利珠单抗(VDZ)治疗的 IBD 患者。采用 Kaplan-Meier 方法结合对数秩检验和 Cox 比例风险进行统计分析。
本研究共纳入了 100 例患者(克罗恩病:62 例,溃疡性结肠炎:31 例,IBD 未分类:7 例),共 127 条治疗线(62 条 UST,65 条 VDZ)。先前抗 TNF 药物的免疫原性并不影响后续乌司奴单抗和维得利珠单抗治疗的持续时间(UST:对数秩检验:=0.95,免疫原性:治疗中止的 HR:0.97[95%CI 0.31-3.04];VDZ:=0.65,HR:0.85[0.41-1.75];总队列[UST 和 VDZ]:=0.62,HR:0.86[0.47-1.57])。硫唑嘌呤联合治疗并未延长治疗持续时间(UST:对数秩检验:=0.77,硫唑嘌呤:HR:1.20[0.34-4.27];VDZ:=0.92,HR:0.58[0.17-1.99];总队列:=0.79,HR:1.10[0.55-2.20])。在这个抗 TNF 治疗经验的队列中,乌司奴单抗治疗的患者比接受维得利珠单抗治疗的患者的治疗持续时间更长(对数秩检验:=0.005,UST:HR:0.43[0.23-0.79])。
抗 TNF 药物的免疫原性并不影响后续乌司奴单抗和维得利珠单抗治疗的持续时间。