作者
Tessa Straatmijer,Vince B C Biemans,Marijn C. Visschedijk,Frank Hoentjen,Annemarie de Vries,Adriaan A. van Bodegraven,Alexander Bodelier,Nanne K H de Boer,Gerard Dijkstra,Noortje Festen,Carmen S. Horjus,Jeroen M. Jansen,Bindia Jharap,W Mares,Fiona D. van Schaik,Cyriel Y. Ponsioen,Tessa E H Römkens,Nidhi Srivastava,Michael MPJA. van der Voorn,Rachel West,J van der Woude,Marije D.J. Wolvers,Marieke Pierik,Andrea E. van der Meulen‐de Jong,Marjolijn Duijvestein,Malena Schlotter,Martine van Workum,Dirk de Jong,Willemijn van Dop,Sander van der Marel,Hayat El Ghabzouri,Kamila Talhaoui,Bas Oldenburg,Nynke Boontje,Herma H. Fidder,Meike M. Hirdes,Rob H. Creemers,Jildou Hoekstra,Jael Smid,Zlatan Mujagic,Marthe François-Verweij,Toos Schakel- van den Berge,Jeroen Maljaars,Rosaline Theeuwen,Denise van den Berg,Suzanne Gerretsen,Xenia Yocarini,Geert R. D’Haens,Mark Löwenberg,Joep Grootjans,Krisztina Gecse,Gerd Bouma,Petra Waaijenberg,Bart Muskens
摘要
Clinicians face difficulty in when and in what order to position biologics and Janus kinase inhibitors in patients with anti-tumor necrosis factor-alpha (TNF) refractory ulcerative colitis (UC). We aimed to compare the effectiveness and safety of vedolizumab and tofacitinib in anti-TNF-exposed patients with UC in our prospective nationwide Initiative on Crohn and Colitis Registry.Patients with UC who failed anti-TNF treatment and initiated vedolizumab or tofacitinib treatment were identified in the Initiative on Crohn and Colitis Registry in the Netherlands. We selected patients with both clinical as well as biochemical or endoscopic disease activity at initiation of therapy. Patients previously treated with vedolizumab or tofacitinib were excluded. Corticosteroid-free clinical remission (Simple Clinical Colitis Activity Index ≤2), biochemical remission (C-reactive protein ≤5 mg/L or fecal calprotectin ≤250 μg/g), and safety outcomes were compared after 52 weeks of treatment. Inverse propensity score-weighted comparison was used to adjust for confounding and selection bias.Overall, 83 vedolizumab- and 65 tofacitinib-treated patients were included. Propensity score-weighted analysis showed that tofacitinib-treated patients were more likely to achieve corticosteroid-free clinical remission and biochemical remission at weeks 12, 24, and 52 compared with vedolizumab-treated patients (odds ratio [OR], 6.33; 95% confidence interval [CI], 3.81-10.50; P < .01; OR, 3.02; 95% CI, 1.89-4.84; P < .01; and OR, 1.86; 95% CI, 1.15-2.99; P = .01; and OR, 3.27; 95% CI, 1.96-5.45; P < .01; OR, 1.87; 95% CI, 1.14-3.07; P = .01; and OR, 1.81; 95% CI, 1.06-3.09; P = .03, respectively). There was no difference in infection rate or severe adverse events.Tofacitinib was associated with superior effectiveness outcomes compared with vedolizumab in anti-TNF-experienced patients with UC along with comparable safety outcomes.