Real-world Comparative Effectiveness of Ustekinumab vs Anti-TNF in Crohn's Disease With Propensity Score Adjustment: Induction Phase Results From the Prospective, Observational RUN-CD Study.


Journal

Inflammatory bowel diseases
ISSN: 1536-4844
Titre abrégé: Inflamm Bowel Dis
Pays: England
ID NLM: 9508162

Informations de publication

Date de publication:
02 11 2023
Historique:
received: 25 06 2022
medline: 8 11 2023
pubmed: 13 1 2023
entrez: 12 1 2023
Statut: ppublish

Résumé

In addition to randomized controlled trials (RCTs), real-world studies on the effectiveness of ustekinumab (UST) in Crohn's disease (CD) are required inasmuch as RCTs are usually confined to selected patients, which may not represent everyday clinical practice. Within the framework of the prospective real-world RUN-CD registry, a total of approximately 900 CD patients from 44 inflammatory bowel disease centers from all over Germany starting a new therapy with UST or other biologics were screened for a real-world evidence (RWE) comparison of CD patients with UST vs antitumor necrosis factor (TNF). A total of 618 CD patients with a nonrandomized biological therapy were qualified for this induction phase effectiveness RUN-CD study of UST vs anti-TNF. To reduce selection bias in estimations of treatment effects, the propensity score with inverse probability of treatment weighting was implemented. The results were reported as odds ratio (OR) and 95% confidence interval (CI). A total of 339 UST and 279 anti-TNF patients were analyzed. The effectiveness of UST vs anti-TNF in terms of clinical remission (UST 65.4% vs anti-TNF 63.0%; OR, 1.11; 95% CI, 0.71-1.74) and steroid-free remission (UST 51.0% vs anti-TNF 53.8%; OR, 0.94; 95% CI, 0.60-1.47) was comparable at the end of induction therapy. Similar results were observed in the bio-naïve and bio-experienced UST vs anti-TNF groups. For both, the remission rates were higher in the bio-naïve than in the bio-experienced groups (P < .05). In this prospective, observational RUN-CD study, the RWE head-to-head comparison of UST vs anti-TNF showed similar induction effectiveness in both groups, remarkably higher than those found in prior RCTs. The higher effectiveness outcome rates observed in patients treated with UST compared with pivotal studies in combination with its known favorable safety profile and an improved HRQoL support UST use as a first-line, advanced therapy in CD.

Sections du résumé

BACKGROUND
In addition to randomized controlled trials (RCTs), real-world studies on the effectiveness of ustekinumab (UST) in Crohn's disease (CD) are required inasmuch as RCTs are usually confined to selected patients, which may not represent everyday clinical practice. Within the framework of the prospective real-world RUN-CD registry, a total of approximately 900 CD patients from 44 inflammatory bowel disease centers from all over Germany starting a new therapy with UST or other biologics were screened for a real-world evidence (RWE) comparison of CD patients with UST vs antitumor necrosis factor (TNF).
METHODS
A total of 618 CD patients with a nonrandomized biological therapy were qualified for this induction phase effectiveness RUN-CD study of UST vs anti-TNF. To reduce selection bias in estimations of treatment effects, the propensity score with inverse probability of treatment weighting was implemented. The results were reported as odds ratio (OR) and 95% confidence interval (CI).
RESULTS
A total of 339 UST and 279 anti-TNF patients were analyzed. The effectiveness of UST vs anti-TNF in terms of clinical remission (UST 65.4% vs anti-TNF 63.0%; OR, 1.11; 95% CI, 0.71-1.74) and steroid-free remission (UST 51.0% vs anti-TNF 53.8%; OR, 0.94; 95% CI, 0.60-1.47) was comparable at the end of induction therapy. Similar results were observed in the bio-naïve and bio-experienced UST vs anti-TNF groups. For both, the remission rates were higher in the bio-naïve than in the bio-experienced groups (P < .05).
CONCLUSIONS
In this prospective, observational RUN-CD study, the RWE head-to-head comparison of UST vs anti-TNF showed similar induction effectiveness in both groups, remarkably higher than those found in prior RCTs.
The higher effectiveness outcome rates observed in patients treated with UST compared with pivotal studies in combination with its known favorable safety profile and an improved HRQoL support UST use as a first-line, advanced therapy in CD.

Autres résumés

Type: plain-language-summary (eng)
The higher effectiveness outcome rates observed in patients treated with UST compared with pivotal studies in combination with its known favorable safety profile and an improved HRQoL support UST use as a first-line, advanced therapy in CD.

Identifiants

pubmed: 36633301
pii: 6986148
doi: 10.1093/ibd/izac271
doi:

Substances chimiques

Ustekinumab FU77B4U5Z0

Types de publication

Observational Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1741-1750

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Crohn’s & Colitis Foundation. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Bernd Bokemeyer (B)

Interdisciplinary Crohn Colitis Centre Minden, Germany.
Clinic of General Internal Medicine I, University Hospital Schleswig-Holstein, Campus Kiel, Germany.
Competence Network IBD, Kiel, Germany.

Sandra Plachta-Danielzik (S)

Competence Network IBD, Kiel, Germany.

Romina di Giuseppe (R)

Competence Network IBD, Kiel, Germany.

Wolfgang Mohl (W)

Center for Gastroenterology Saar MVZ, Saarbrücken, Germany.

Niels Teich (N)

Gastroenterology Practice, Leipzig, Germany.

Martin Hoffstadt (M)

Gastroenterology Practice, Iserlohn, Germany.

Axel Schweitzer (A)

Gastroenterology Practice, Münster, Germany.

Manfred von der Ohe (M)

Gastroenterology Practice, Herne, Germany.

Annika Gauss (A)

Department of Gastroenterology, Internal Medicine IV, University Hospital of Heidelberg, Germany.

Raja Atreya (R)

Department of Medicine, Medical Clinic 1, University Hospital Erlangen, University of Erlangen-Nürnberg, Germany.

Thomas Krause (T)

Gastroenterology Practice, Kassel, Germany.

Irina Blumenstein (I)

Department of Gastroenterology and Clinical Nutrition, Johann Wolfgang Goethe University Clinic, Frankfurt, Germany.

Petra Hartmann (P)

Gastroenterology Practice, Minden, Germany.

Stefan Schreiber (S)

Clinic of General Internal Medicine I, University Hospital Schleswig-Holstein, Campus Kiel, Germany.

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