Comparison between tofacitinib and ustekinumab as a third-line therapy in refractory ulcerative colitis: A multicenter international study

被引:5
作者
Allocca, Mariangela [1 ,2 ,26 ,27 ]
Catalano, Gaia [1 ,2 ]
Savarino, Edoardo V. [3 ]
Chaparro, Maria [4 ,5 ]
Levartovsky, Asaf [6 ]
Michalopoulos, George [7 ]
Viazis, Nikos [8 ]
Fousekis, Fotis S. [9 ]
Psistakis, Andreas [10 ]
Noviello, Daniele [11 ]
do Nascimento, Catarina Neto [12 ]
Caron, Benedicte [13 ,14 ]
Kitsou, Vassiliki [15 ]
Bamias, Giorgos [15 ]
Garcia, Maria Jose [16 ]
Zacharopoulou, Eirini [17 ]
Foteinogiannopoulou, Kalliopi [18 ]
D'Amico, Ferdinando [1 ,2 ]
Koutroubakis, Ioannis [18 ]
Ellul, Pierre [19 ]
Tzouvala, Maria [17 ]
Peyrin-Biroulet, Laurent [13 ,14 ,20 ]
Torres, Joana [12 ]
Caprioli, Flavio [11 ,21 ]
Karmiris, Konstantinos [10 ]
Theodoropoulou, Angeliki [10 ]
Katsanos, Konstantinos H. [9 ]
Christodoulou, Dimitrios K. [9 ]
Mantzaris, Gerassimos J. [8 ]
Kopylov, Uri [6 ]
Gisbert, Javier P. [4 ,5 ]
Danese, Silvio [1 ,2 ,22 ]
Magro, Fernando [23 ]
Carla, Fornari [24 ]
Fiorino, Gionata [22 ,25 ]
机构
[1] IRCCS Hosp San Raffaele, Gastroenterol & Endoscopy, Milan, Italy
[2] Univ Vita Salute San Raffaele, Milan, Italy
[3] Univ Padua, Dept Surg Oncol & Gastroenterol, Div Gastroenterol, Padua, Italy
[4] Hosp Univ Princesa, Univ Autonoma Madrid UAM, Inst Invest Sanitaria Princesa IIS Princesa, Madrid, Spain
[5] Ctr Invest Biomed Red Enfermedades Hepat & Digest, Madrid, Spain
[6] Tel Aviv Univ, Sheba Med Ctr, Gastroenterol, Tel Hashomer, Tel Aviv, Israel
[7] Gen Hosp Athens G Gennimatas, Athens, Greece
[8] Evangelismos PolyklinikiGHA, Athens, Greece
[9] Univ Ioannina, Fac Med, Sch Hlth Sci, Dept Internal Med,Div Gastroenterol, Ioannina, Greece
[10] Venizeleio Gen Hosp, Gastroenterol, Iraklion, Greece
[11] Univ Milan, Universita` Studi Milano, Milan, Italy
[12] Hosp Beatriz Angelo, Gastroenterol, Loures, Portugal
[13] Univ Hosp Nancy, Univ Lorraine, Dept Gastroenterol, Nancy, France
[14] Univ Lorraine, Univ Hosp Nancy, Inserm, NGERE 1256, Nancy, France
[15] Natl & Kapodistrian Univ Athens, Sotiria Hosp, Acad Dept Internal Med 3, GI Unit, Athens, Greece
[16] Hosp Univ Marques de Valdecilla, Gastroenterol & Hepatol Dept, Santander, Spain
[17] Gen Hosp Nikaia & Piraeus Agios Panteleimon Gen Ho, Gastroenterol, Athens, Greece
[18] Univ Crete, Univ Hosp Heraklion, Med Sch, Gastroenterol Dept, Iraklion, Greece
[19] Mater Dei Hosp, Gastroenterol, Msida, Malta
[20] Paris IBD Ctr, Grp Hospitalier Ambroise Pare Hartmann, Neuilly Sur Seine, France
[21] Fdn IRCCS CaGranda Osped Maggiore Policlin, Gastroenterol & Endoscopy Unit, Milan, Italy
[22] Univ Vita Salute San Raffaele, Milan, Italy
[23] Univ Porto, Fac Med, Unit Pharmacol & Therapeut, Gastroenterol & Biomed, Porto, Portugal
[24] Univ Milano Bicocca, Res Ctr Publ Hlth, Dept Med & Surg, Monza, Italy
[25] San Camillo Forlanini Hosp, Gastroenterol & Digest Endoscopy, Rome, Italy
[26] IRCCS Hosp San Raffaele, Dept Gastroenterol & Endoscopy, Via Olgettina 60, I-20132 Milan, Italy
[27] Univ Vita Salute San Raffaele, Via Olgettina 60, I-20132 Milan, Italy
关键词
biologics; inflammatory bowel disease; tofacitinib; MAINTENANCE THERAPY; INDUCTION;
D O I
10.1002/ueg2.12492
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Ustekinumab and tofacitinib have recently been approved for the management of moderate to severe ulcerative colitis (UC). However, there is no evidence on how they should be positioned in the therapeutic algorithm. The aim of this study was to compare tofacitinib and ustekinumab as third-line therapies in UC patients in whom anti-TNF and vedolizumab had failed. Methods: This was a multicenter retrospective observational study. The primary outcome was disease progression, defined as the need for steroids, therapy escalation, UC-related hospitalization and/or surgery. Secondary outcomes were clinical remission, normalization of C-reactive protein, endoscopic remission, treatment withdrawal, and adverse events. Results: One-hundred seventeen UC patients were included in the study and followed for a median time of 11.6 months (q(1) -q(3,) 5.5-18.7). Overall, 65% of patients were treated with tofacitinib and 35% with ustekinumab. In the entire study cohort, 63 patients (54%) had disease progression during the follow-up period. Treatment with ustekinumab predicted increased risk of disease progression compared to treatment with tofacitinib in Cox regression analysis (HR: 1.93 [95% CI: 1.06-3.50] p = 0.030). Twenty-eight (68%) patients in the ustekinumab group and 35 (46%) in the tofacitinib group had disease progression over the follow-up period (log-rank test, p < 0.054). No significant differences were observed for the secondary outcomes. Six and 22 adverse events occurred in the ustekinumab and tofacitinib groups, respectively (15% vs. 31%, p = 0.11). Conclusions: Tofacitinib was more efficacious in reducing disease progression than ustekinumab in this cohort of refractory UC patients. However, prospective head-to-head clinical trials are needed as to confirm these data.
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收藏
页码:543 / 551
页数:9
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