Five-year Safety Data From OPUS, a European Observational Safety Registry for Adults With Ulcerative Colitis Treated With Originator Infliximab [Remicade®] or Conventional Therapy.


Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
19 Sep 2019
Historique:
pubmed: 28 2 2019
medline: 13 2 2020
entrez: 28 2 2019
Statut: ppublish

Résumé

The Observational Postmarketing Ulcerative colitis Study [OPUS] was conducted to obtain the first long-term [5 years] safety data assessing treatment with originator infliximab versus conventional therapies in patients with ulcerative colitis [UC] in real-world clinical practice. The OPUS registry was a prospective, non-randomised, observational study that measured adverse events in nine prespecified categories of interest in UC patients whose treatment with either originator infliximab or conventional therapy [defined as initiation or dose-increase of corticosteroids and/or immunosuppressants] was determined by their treating physician. Data for 2239 patients were available: N = 1180 enrolled to conventional therapy [including N = 296 who switched to originator infliximab during follow-up] and N = 1059 enrolled to originator infliximab. Patients in the originator infliximab group, compared with the conventional therapy group, had more severe disease at baseline, based on partial Mayo score [PMS]: 46.0% of patients in the originator infliximab group had severe disease (PMS of 7-9 [out of 9]), compared with 30.5% in the conventional therapy group. In adjusted time-to-event analyses, enrolment into the originator infliximab group was associated with a higher risk of serious infection (hazard ratio = 1.98 [95% confidence interval: 1.34, 2.91; p <0.001]) compared with enrolment into the conventional therapy group. No notable risk differences between groups were identified for haematological disorder, autoimmune disorder, malignancy/lymphoproliferative disorder, hepatobiliary disorder or fatality. UC patients treated with infliximab had higher risk for serious infection, compared with conventional therapies. No new safety concerns were observed with originator infliximab in the OPUS registry. [ClinicalTrials.gov: NCT00705484.].

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
The Observational Postmarketing Ulcerative colitis Study [OPUS] was conducted to obtain the first long-term [5 years] safety data assessing treatment with originator infliximab versus conventional therapies in patients with ulcerative colitis [UC] in real-world clinical practice.
METHODS METHODS
The OPUS registry was a prospective, non-randomised, observational study that measured adverse events in nine prespecified categories of interest in UC patients whose treatment with either originator infliximab or conventional therapy [defined as initiation or dose-increase of corticosteroids and/or immunosuppressants] was determined by their treating physician.
RESULTS RESULTS
Data for 2239 patients were available: N = 1180 enrolled to conventional therapy [including N = 296 who switched to originator infliximab during follow-up] and N = 1059 enrolled to originator infliximab. Patients in the originator infliximab group, compared with the conventional therapy group, had more severe disease at baseline, based on partial Mayo score [PMS]: 46.0% of patients in the originator infliximab group had severe disease (PMS of 7-9 [out of 9]), compared with 30.5% in the conventional therapy group. In adjusted time-to-event analyses, enrolment into the originator infliximab group was associated with a higher risk of serious infection (hazard ratio = 1.98 [95% confidence interval: 1.34, 2.91; p <0.001]) compared with enrolment into the conventional therapy group. No notable risk differences between groups were identified for haematological disorder, autoimmune disorder, malignancy/lymphoproliferative disorder, hepatobiliary disorder or fatality.
CONCLUSIONS CONCLUSIONS
UC patients treated with infliximab had higher risk for serious infection, compared with conventional therapies. No new safety concerns were observed with originator infliximab in the OPUS registry. [ClinicalTrials.gov: NCT00705484.].

Identifiants

pubmed: 30809631
pii: 5365571
doi: 10.1093/ecco-jcc/jjz048
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Gastrointestinal Agents 0
Immunosuppressive Agents 0
Infliximab B72HH48FLU

Banques de données

ClinicalTrials.gov
['NCT00705484']

Types de publication

Comparative Study Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1148-1157

Informations de copyright

Copyright © 2019 European Crohn’s and Colitis Organisation (ECCO). Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Julián Panés (J)

Department of Gastroenterology, Hospital Clínic de Barcelona, IDIBAPS, CIBERehd, Barcelona, Spain.

James O Lindsay (JO)

Department of Gastrointestinal and Liver Services, Royal London Hospital, Barts Health NHS Trust, London, UK.

Niels Teich (N)

Innere Medizin/Gastroenterologie, Internistische Gemeinschaftspraxis, Leipzig, Germany.

Stefan Lindgren (S)

Department of Gastroenterology, Lund University, Malmo, Sweden.

Jean-Frédéric Colombel (JF)

Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Freddy Cornillie (F)

Global Medical Affairs, MSD International, Kriens-Luzern, Switzerland.

Heather Ann Flynn (HA)

MRL, Merck & Co., Inc., Kenilworth, NJ, USA.

Susan Huyck (S)

MRL, Merck & Co., Inc., Kenilworth, NJ, USA.

Paul Stryszak (P)

MRL, Merck & Co., Inc., Kenilworth, NJ, USA.

Ruji Yao (R)

MRL, Merck & Co., Inc., Kenilworth, NJ, USA.

George Philip (G)

MRL, Merck & Co., Inc., Kenilworth, NJ, USA.

Walter Reinisch (W)

Klinische Abt. Gastroenterologie & Hepatologie, Universitätsklinik für Innere Medizin III, Vienna, Austria.

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Classifications MeSH