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Clinical effectiveness of golimumab in ulcerative colitis: a prospective multicentre study based on the Swedish IBD Quality Register, SWIBREG
Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden; Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.ORCID iD: 0000-0002-1046-383x
Örebro University, School of Medical Sciences. Department of Gastroenterology.ORCID iD: 0000-0002-6316-5027
GHP Gastro Center Skåne, Lund, Sweden.
Department of Gastroenterology, Danderyd Hospital, Stockholm, Sweden.
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2021 (English)In: Scandinavian Journal of Gastroenterology, ISSN 0036-5521, E-ISSN 1502-7708, Vol. 56, no 11, p. 1304-1311Article in journal (Refereed) Published
Abstract [en]

OBJECTIVES: Clinical trials demonstrated that golimumab is effective in anti-TNF naïve patients with ulcerative colitis. We aimed to assess the clinical effectiveness of golimumab in a real-world setting.

MATERIALS AND METHODS: This was a prospective cohort study, conducted at 16 Swedish hospitals. Data were collected using an electronic case report form. Patients with active ulcerative colitis, defined as Mayo endoscopic subscore ≥2 were eligible for inclusion. The primary outcomes were clinical effectiveness at 12 weeks and 52 weeks, i.e. response (defined as a decrease in Mayo score by ≥3 points or 30% from baseline) and remission (defined as a Mayo score of ≤2 with no individual subscores >1).

RESULTS: Fifty patients were included. At study entry, 70% were previously exposed to anti-TNF, 16% to vedolizumab, and 96% to immunomodulators. The 12 and 52-week drug continuation rates were 37/50 (74%) and 23/50 (46%), respectively. The 12-week response rate was 14/50 (28%), the remission rate, 8/50 (16%) and the corresponding figures at week 52 were 13/50 (26%) and 10/50 (20%). Among patients who continued golimumab, the median Mayo score decreased from 7 (6-9) at baseline to 1 (0-5) at 52 weeks (p < .01) and the faecal calprotectin decreased from 862 (335-1759) µg/g to 90 (34-169) µg/g (p < .01). Clinical response at week 12 was highly predictive of clinical remission at week 52 (adjusted OR: 73.1; 95% CI: 4.5‒1188.9).

CONCLUSIONS: The majority of golimumab treated patients represented a treatment refractory patient-group. Despite this, our results confirm that golimumab is an effective therapy in ulcerative colitis.

Place, publisher, year, edition, pages
Taylor & Francis, 2021. Vol. 56, no 11, p. 1304-1311
Keywords [en]
Golimumab, clinical effectiveness, inflammatory bowel disease, ulcerative colitis
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-93826DOI: 10.1080/00365521.2021.1963466ISI: 000686823300001PubMedID: 34415803Scopus ID: 2-s2.0-85113310015OAI: oai:DiVA.org:oru-93826DiVA, id: diva2:1586851
Note

Funding agencies:

MSD

Swedish government's agreement on medical training and research OLL-836791  OLL-929900

Available from: 2021-08-23 Created: 2021-08-23 Last updated: 2024-11-19Bibliographically approved
In thesis
1. Biological treatment in inflammatory bowel disease: clinical and therapeutic aspects
Open this publication in new window or tab >>Biological treatment in inflammatory bowel disease: clinical and therapeutic aspects
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Biological therapy has emerged as an important treatment modality for inflammatory bowel disease (IBD). Despite the prevailing trend, there contin­ues to be a lack of guidelines for selecting a suitable biological drug for a specific patient group. Register data are valuable sources for real-world studies of treatment outcomes across diverse patient groups. This thesis in­cludes four observational cohort studies assessing clinical and therapeutic aspects of biological treatment in patients with IBD, covering the main sub­types Crohn's disease and ulcerative colitis. The overarching aim is to ad­vance understanding of the effectiveness and safety of biological treatment in patients diagnosed with IBD.

Study I examined anti-tumour necrosis factor (anti-TNF) drug continuation rates in 955 patients with IBD that were recorded in the Swedish IBD regis­ter (SWIBREG). Infliximab (vs adalimumab) discontinuation was higher when used as first- and second-line treatment in patients with Crohn's dis­ease. Study II examined the use of golimumab in ulcerative colitis. Most (70%) of the 50 study patients were previously exposed to anti-TNF. After 1 year, 23 (46%) patients were still on golimumab treatment and improve­ments in clinical and biochemical markers were seen. Study III investigated long-term outcomes of vedolizumab treatment in patients participating in the extension of the Swedish observational study on vedolizumab, focusing on its effectiveness and use of healthcare resources in patients with IBD (SVEAH). Patients who initially responded to vedolizumab treatment and continued it beyond 1 year experienced high rates of clinical remission and improved quality of life measures after 3 years. Few serious adverse events were reported. Study IV examined correlations between baseline clinical characteristics, serum proteins, and drug levels post-induction. Four pro­teins of interest correlated with s-adalimumab levels.

This thesis proposes that the clinical and biochemical characterisation of patients with IBD can contribute to informed decision-making in biological treatment.

Place, publisher, year, edition, pages
Örebro: Örebro University, 2024. p. 132
Series
Örebro Studies in Medicine, ISSN 1652-4063 ; 308
Keywords
inflammatory bowel disease, Crohn's disease, ulcerative colitis, real-world data, SWIBREG, register-based studies, biological treatment, anti-TNF, integrin inhibitor, clinical effectiveness, biochemical data
National Category
General Practice
Identifiers
urn:nbn:se:oru:diva-116240 (URN)9789175296104 (ISBN)9789175296111 (ISBN)
Public defence
2024-12-12, Örebro universitet, Campus USÖ, Tidefeltsalen, Södra Grev Rosengatan 32, Örebro, 09:15 (English)
Opponent
Supervisors
Available from: 2024-09-24 Created: 2024-09-24 Last updated: 2024-12-16Bibliographically approved

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Eriksson, CarlVisuri, IsabellaBergemalm, DanielHalfvarson, Jonas

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