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

BackgroundFilgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.AimsThe aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of t...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2024-09, Vol.60 (5), p.563-584
Hauptverfasser: Feagan, Brian G, Matsuoka, Katsuyoshi, Rogler, Gerhard, Laharie, David, Vermeire, Séverine, Danese, Silvio, Loftus, Edward V, Beales, Ian, Schreiber, Stefan, Hyo Jong Kim, Faes, Margaux, de Haas, Angela, Masior, Tomasz, Rudolph, Christine, Laurent Peyrin‐Biroulet
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container_end_page 584
container_issue 5
container_start_page 563
container_title Alimentary pharmacology & therapeutics
container_volume 60
creator Feagan, Brian G
Matsuoka, Katsuyoshi
Rogler, Gerhard
Laharie, David
Vermeire, Séverine
Danese, Silvio
Loftus, Edward V
Beales, Ian
Schreiber, Stefan
Hyo Jong Kim
Faes, Margaux
de Haas, Angela
Masior, Tomasz
Rudolph, Christine
Laurent Peyrin‐Biroulet
description BackgroundFilgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.AimsThe aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535).MethodsIn 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.ResultsData 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.ConclusionsFilgotinib 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.
doi_str_mv 10.1111/apt.18158
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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.ResultsData 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.ConclusionsFilgotinib 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.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/apt.18158</identifier><language>eng</language><publisher>Chichester: Wiley Subscription Services, Inc</publisher><subject>Biomarkers ; Disease control ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Janus kinase ; Quality of life ; Remission ; Safety ; Ulcerative colitis</subject><ispartof>Alimentary pharmacology &amp; therapeutics, 2024-09, Vol.60 (5), p.563-584</ispartof><rights>2024. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Feagan, Brian G</creatorcontrib><creatorcontrib>Matsuoka, Katsuyoshi</creatorcontrib><creatorcontrib>Rogler, Gerhard</creatorcontrib><creatorcontrib>Laharie, David</creatorcontrib><creatorcontrib>Vermeire, Séverine</creatorcontrib><creatorcontrib>Danese, Silvio</creatorcontrib><creatorcontrib>Loftus, Edward V</creatorcontrib><creatorcontrib>Beales, Ian</creatorcontrib><creatorcontrib>Schreiber, Stefan</creatorcontrib><creatorcontrib>Hyo Jong Kim</creatorcontrib><creatorcontrib>Faes, Margaux</creatorcontrib><creatorcontrib>de Haas, Angela</creatorcontrib><creatorcontrib>Masior, Tomasz</creatorcontrib><creatorcontrib>Rudolph, Christine</creatorcontrib><creatorcontrib>Laurent Peyrin‐Biroulet</creatorcontrib><title>Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4years of follow‐up in the SELECTION open‐label long‐term extension study</title><title>Alimentary pharmacology &amp; therapeutics</title><description>BackgroundFilgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.AimsThe aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535).MethodsIn 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.ResultsData 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.ConclusionsFilgotinib 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.</description><subject>Biomarkers</subject><subject>Disease control</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Janus kinase</subject><subject>Quality of life</subject><subject>Remission</subject><subject>Safety</subject><subject>Ulcerative colitis</subject><issn>0269-2813</issn><issn>1365-2036</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNj79OAzEMhyMEEuXPwBtYYm5J7ui1Za2KqFTBQPcqvTolVS4-El_hNh6BR0Q8CbmKgREvtvTZ-n4W4krJgUp1o2seqLEajo9ET-XFsJ_JvDgWPZkVk342VvmpOItxJ6UsRjLria8F-e33xydjqCBqg9yC9htAY2ypyxbIgLFuS2y9XYOhAPyCwAE1V-i54xVtMGhG1wITRNxj6GZdst0jNK7saDeW5CzbeAdzn3y2Sibt2mgjmEAVNHV3f9uiDvHgJefoLYVLwPqD93m2mE2X86dHoBp9Qk6v0YH78wS-M_poyUPkZtNeiBOjXcTL334uru9ny-lDvw702mDk1Y6akHLEVS4nWa7UqFD5_7Z-ADLFfZY</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Feagan, Brian G</creator><creator>Matsuoka, Katsuyoshi</creator><creator>Rogler, Gerhard</creator><creator>Laharie, David</creator><creator>Vermeire, Séverine</creator><creator>Danese, Silvio</creator><creator>Loftus, Edward V</creator><creator>Beales, Ian</creator><creator>Schreiber, Stefan</creator><creator>Hyo Jong Kim</creator><creator>Faes, Margaux</creator><creator>de Haas, Angela</creator><creator>Masior, Tomasz</creator><creator>Rudolph, Christine</creator><creator>Laurent Peyrin‐Biroulet</creator><general>Wiley Subscription Services, Inc</general><scope>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>M7N</scope></search><sort><creationdate>20240901</creationdate><title>Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4years of follow‐up in the SELECTION open‐label long‐term extension study</title><author>Feagan, Brian G ; Matsuoka, Katsuyoshi ; Rogler, Gerhard ; Laharie, David ; Vermeire, Séverine ; Danese, Silvio ; Loftus, Edward V ; Beales, Ian ; Schreiber, Stefan ; Hyo Jong Kim ; Faes, Margaux ; de Haas, Angela ; Masior, Tomasz ; Rudolph, Christine ; Laurent Peyrin‐Biroulet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_30923117613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biomarkers</topic><topic>Disease control</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory bowel diseases</topic><topic>Janus kinase</topic><topic>Quality of life</topic><topic>Remission</topic><topic>Safety</topic><topic>Ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feagan, Brian G</creatorcontrib><creatorcontrib>Matsuoka, Katsuyoshi</creatorcontrib><creatorcontrib>Rogler, Gerhard</creatorcontrib><creatorcontrib>Laharie, David</creatorcontrib><creatorcontrib>Vermeire, Séverine</creatorcontrib><creatorcontrib>Danese, Silvio</creatorcontrib><creatorcontrib>Loftus, Edward V</creatorcontrib><creatorcontrib>Beales, Ian</creatorcontrib><creatorcontrib>Schreiber, Stefan</creatorcontrib><creatorcontrib>Hyo Jong Kim</creatorcontrib><creatorcontrib>Faes, Margaux</creatorcontrib><creatorcontrib>de Haas, Angela</creatorcontrib><creatorcontrib>Masior, Tomasz</creatorcontrib><creatorcontrib>Rudolph, Christine</creatorcontrib><creatorcontrib>Laurent Peyrin‐Biroulet</creatorcontrib><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feagan, Brian G</au><au>Matsuoka, Katsuyoshi</au><au>Rogler, Gerhard</au><au>Laharie, David</au><au>Vermeire, Séverine</au><au>Danese, Silvio</au><au>Loftus, Edward V</au><au>Beales, Ian</au><au>Schreiber, Stefan</au><au>Hyo Jong Kim</au><au>Faes, Margaux</au><au>de Haas, Angela</au><au>Masior, Tomasz</au><au>Rudolph, Christine</au><au>Laurent Peyrin‐Biroulet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4years of follow‐up in the SELECTION open‐label long‐term extension study</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><date>2024-09-01</date><risdate>2024</risdate><volume>60</volume><issue>5</issue><spage>563</spage><epage>584</epage><pages>563-584</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>BackgroundFilgotinib, an oral, once‐daily, Janus kinase 1 preferential inhibitor, is an approved treatment for moderately to severely active ulcerative colitis.AimsThe aim of this study is to assess the safety and efficacy of continued filgotinib therapy over ~4 years in the long‐term extension of the phase 2b/3 SELECTION trial (SELECTIONLTE; NCT02914535).MethodsIn 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.ResultsData 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.ConclusionsFilgotinib 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.</abstract><cop>Chichester</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/apt.18158</doi></addata></record>
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source Wiley Journals; EZB-FREE-00999 freely available EZB journals
subjects Biomarkers
Disease control
Inflammatory bowel disease
Inflammatory bowel diseases
Janus kinase
Quality of life
Remission
Safety
Ulcerative colitis
title Long‐term safety and efficacy of filgotinib for the treatment of moderately to severely active ulcerative colitis: Interim analysis from up to 4years of follow‐up in the SELECTION open‐label long‐term extension study
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