Real-life treatment persistence and treatment outcomes of Finnish patients with inflammatory bowel disease receiving vedolizumab as first-line biological treatment

dc.contributor.authorYlisaukko-oja, Tero
dc.contributor.authoraf Björkesten, Clas-Göran
dc.contributor.authorEberl, Anja
dc.contributor.authorNuutinen, Heikki
dc.contributor.authorJussila, Airi
dc.contributor.authorMolander, Pauliina
dc.contributor.authorKoskela, Ritva
dc.contributor.authorBlomster, Timo
dc.contributor.authorPajala, Markku
dc.contributor.authorIlus, Tuire
dc.contributor.authorHaiko, Paula
dc.contributor.authorKovac, Bianca
dc.contributor.authorSilvola, Saija
dc.contributor.authorSmith, Sarah
dc.contributor.authorJokelainen, Jari
dc.contributor.authorSipponen, Taina
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.converis.publication-id456842465
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/456842465
dc.date.accessioned2025-08-28T02:32:46Z
dc.date.available2025-08-28T02:32:46Z
dc.description.abstract<p><strong>Purpose: </strong>To analyze treatment persistence and treatment outcomes of vedolizumab as first-line biological treatment in Crohn's disease (CD) and ulcerative colitis (UC) patients in a Finnish real-world setting.</p><p><strong>Methods: </strong>Observational, retrospective, multi-center chart review study that included adult CD and UC patients initiating vedolizumab as first-line biological treatment between 2014 and 2020.</p><p><strong>Results: </strong>The cohort consisted of 54 CD and 69 UC patients. At month 12, treatment persistence was 84.9 % in CD and 64.7 % in UC. Most vedolizumab discontinuations (CD, n = 11; UC, n = 26) were due to inefficacy. Discontinuations due to adverse events were rare (n < 5). Efficacy improvements were observed in treatment persistent patients at 12 months vs. baseline in the Harvey-Bradshaw Index (CD, 1.8 vs. 3.9, p = 0.001), Partial Mayo Score (UC, 1.0 vs. 4.9, p < 0.001), Physician's Global Assessment (CD, 0.9 vs. 1.8, p < 0.001; UC, 0.4 vs. 2.1, p < 0.001), along with positive endoscopic and biochemical outcomes. Clinical remission was 90.9 % vs. 63.0 % for CD, and 81.6 % vs. 12.3 % for UC, while corticosteroid use was 15.9 % vs. 53.7 % for CD, and 14.6 % vs. 92.8 % for UC at 12 months and baseline, respectively.</p><p><strong>Conclusion: </strong>Vedolizumab was associated with improvements in efficacy, endoscopic activity, biochemical parameters, and decreased corticosteroid burden when used as a first-line biological treatment.</p>
dc.identifier.eissn2405-8440
dc.identifier.jour-issn2405-8440
dc.identifier.olddbid209274
dc.identifier.oldhandle10024/192301
dc.identifier.urihttps://www.utupub.fi/handle/11111/41443
dc.identifier.urnURN:NBN:fi-fe2025082788273
dc.language.isoen
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumbere32432
dc.relation.doi10.1016/j.heliyon.2024.e32432
dc.relation.ispartofjournalHeliyon
dc.relation.issue12
dc.relation.volume10
dc.source.identifierhttps://www.utupub.fi/handle/10024/192301
dc.titleReal-life treatment persistence and treatment outcomes of Finnish patients with inflammatory bowel disease receiving vedolizumab as first-line biological treatment
dc.year.issued2024

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