Long-term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4 years of follow-up in the SELECTION open-label long-term extension study

被引:1
|
作者
Feagan, Brian G. [1 ,2 ]
Matsuoka, Katsuyoshi [3 ]
Rogler, Gerhard [4 ]
Laharie, David [5 ]
Vermeire, Severine [6 ]
Danese, Silvio [7 ,8 ]
Loftus Jr, Edward V. [9 ]
Beales, Ian [10 ,11 ]
Schreiber, Stefan [12 ]
Kim, Hyo Jong [13 ]
Faes, Margaux [14 ]
de Haas, Angela [15 ]
Masior, Tomasz [16 ]
Rudolph, Christine [15 ]
Peyrin-Biroulet, Laurent [17 ,18 ,19 ,20 ,21 ,22 ]
机构
[1] Alimentiv Inc, London, ON, Canada
[2] Western Univ, London, ON, Canada
[3] Toho Univ, Sakura Med Ctr, Dept Internal Med, Div Gastroenterol & Hepatol, Chiba, Japan
[4] Univ Zurich, Univ Hosp Zurich, Dept Gastroenterol & Hepatol, Zurich, Switzerland
[5] Univ Bordeaux, Hosp Ctr Univ Bordeaux, Magellan Med Surg Ctr, Haut Leveque Hosp,Gastroenterol Dept, Bordeaux, France
[6] UZ Leuven, Dept Gastroenterol & Hepatol, Leuven, Belgium
[7] IRCCS Hosp San Raffaele, Dept Gastroenterol & Endoscopy, Milan, Italy
[8] Univ Vita Salute San Raffaele, Milan, Italy
[9] Mayo Clin, Coll Med & Sci, Div Gastroenterol & Hepatol, Rochester, MN USA
[10] Norfolk & Norwich Univ Hosp NHS Fdn Trust, Dept Gastroenterol, Norwich, England
[11] Univ East Anglia, Norwich, England
[12] Univ Kiel, Univ Hosp Schleswig Holstein, Dept Internal Med 1, Kiel, Germany
[13] Kyung Hee Univ, Ctr Crohns & Colitis, Dept Gastroenterol, Seoul, South Korea
[14] Galapagos NV, Mechelen, Belgium
[15] Galapagos NV, Leiden, Netherlands
[16] Galapagos GmbH, Basel, Switzerland
[17] Nancy Univ Hosp, Dept Gastroenterol, Nancy, France
[18] Univ Lorraine, INSERM, NGERE, Nancy, France
[19] Nancy Univ Hosp, INFINY Inst, Nancy, France
[20] Nancy Univ Hosp, FHU CURE, Nancy, France
[21] Private Hosp Grp Ambroise Pare Hartmann, Paris IBD Ctr, Neuilly Sur Seine, France
[22] McGill Univ, Hlth Ctr, Div Gastroenterol & Hepatol, Montreal, PQ, Canada
关键词
PHASE; 2B/3; SELECTION;
D O I
10.1111/apt.18158
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Filgotinib, an oral, once-daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis. Aims: The aim of this study is to assess the safety and efficacy of continued filgotinib therapy over similar to 4 years in the long-term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535). Methods: In this interim analysis of SELECTIONLTE, SELECTION completers (week 10 responders to filgotinib who completed the maintenance study) continued their assigned treatment (double-blind filgotinib 200 mg [FIL200] or filgotinib 100 mg) and SELECTION week 10 non-responders received open-label FIL200. We assessed safety by adverse events (AEs), and efficacy by partial Mayo Clinic Score (pMCS), inflammatory biomarkers and health-related quality of life (HRQoL). We compared safety and efficacy between achievers and non-achievers of a multi-component endpoint, comprehensive disease control (CDC), comprising symptomatic, endoscopic, inflammatory biomarker and HRQoL improvements. Results: Data for completers (n = 250) and non-responders (n = 372) were reported for <= 202 weeks. AE occurrences were low and consistent with previous analyses. The as-observed proportion of FIL200-treated patients in pMCS, biomarker and HRQoL remission during SELECTIONLTE remained high among completers (week 144: 80.0%, 86.4% and 86.0%, respectively) and increased among non-responders (week 192: 62.1%, 76.7% and 59.3%, respectively). Significantly higher proportions of CDC achievers at SELECTION week 58 achieved pMCS, IBDQ and corticosteroid-free pMCS remission than non-achievers, up to LTE week 96. Conclusions: Filgotinib induced and maintained symptomatic remission and improved HRQoL over 4 years. Safety results showed a proven long-term benefit-risk profile. FIL200-treated CDC achievers had better long-term outcomes than non-achievers.
引用
收藏
页码:563 / 584
页数:22
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