Higher vs Standard Adalimumab Induction and Maintenance Dosing Regimens for Treatment of Ulcerative Colitis: SERENE UC Trial Results.

Adalimumab Clinical Trial Result Inflammatory Bowel Disease Moderately to Severely Active Ulcerative Colitis Monoclonal Antibody

Journal

Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630

Informations de publication

Date de publication:
06 2022
Historique:
received: 20 07 2021
revised: 02 02 2022
accepted: 20 02 2022
pubmed: 2 3 2022
medline: 18 5 2022
entrez: 1 3 2022
Statut: ppublish

Résumé

SERENE UC (Study of a Novel Approach to Induction and Maintenance Dosing With Adalimumab in Patients With Moderate to Severe Ulcerative Colitis) evaluated the efficacy of higher adalimumab induction and maintenance dose regimens in patients with ulcerative colitis. This phase 3, double-blind, randomized trial included induction and maintenance studies, with a main study (ex-Japan) and Japan substudy. Eligible patients (18-75 years, full Mayo score 6-12, centrally read endoscopy subscore 2-3) were randomized 3:2 to higher induction regimen (adalimumab 160 mg at weeks 0, 1, 2, and 3) or standard induction regimen (160 mg at week 0 and 80 mg at week 2); all received 40 mg at weeks 4 and 6. At week 8, all patients were rerandomized 2:2:1 (main study) to 40 mg every week (ew), 40 mg every other week (eow), or exploratory therapeutic drug monitoring; or 1:1 (Japan substudy) to 40 mg ew or 40 mg eow maintenance regimens. In the main study, 13.3% vs 10.9% of patients receiving the higher induction regimen vs standard induction regimen achieved clinical remission (full Mayo score ≤2 with no subscore >1) at week 8 (induction primary end point; P = .265); among week-8 responders, 39.5% vs 29.0% receiving 40 mg ew vs 40 mg eow achieved clinical remission at week 52 (maintenance primary end point; P = .069). In the integrated (main + Japan) population, 41.1% vs 30.1% of week-8 responders receiving 40 mg ew vs 40 mg eow achieved clinical remission at week 52 (nominal P = .045). Safety profiles were comparable between dosing regimens. Although primary end points were not met, a >10% absolute difference in clinical remission was demonstrated with higher adalimumab maintenance dosing. Higher dosing regimens were generally well tolerated and consistent with the known safety profile of adalimumab in ulcerative colitis. gov, Number: NCT002209456.

Sections du résumé

BACKGROUND & AIMS
SERENE UC (Study of a Novel Approach to Induction and Maintenance Dosing With Adalimumab in Patients With Moderate to Severe Ulcerative Colitis) evaluated the efficacy of higher adalimumab induction and maintenance dose regimens in patients with ulcerative colitis.
METHODS
This phase 3, double-blind, randomized trial included induction and maintenance studies, with a main study (ex-Japan) and Japan substudy. Eligible patients (18-75 years, full Mayo score 6-12, centrally read endoscopy subscore 2-3) were randomized 3:2 to higher induction regimen (adalimumab 160 mg at weeks 0, 1, 2, and 3) or standard induction regimen (160 mg at week 0 and 80 mg at week 2); all received 40 mg at weeks 4 and 6. At week 8, all patients were rerandomized 2:2:1 (main study) to 40 mg every week (ew), 40 mg every other week (eow), or exploratory therapeutic drug monitoring; or 1:1 (Japan substudy) to 40 mg ew or 40 mg eow maintenance regimens.
RESULTS
In the main study, 13.3% vs 10.9% of patients receiving the higher induction regimen vs standard induction regimen achieved clinical remission (full Mayo score ≤2 with no subscore >1) at week 8 (induction primary end point; P = .265); among week-8 responders, 39.5% vs 29.0% receiving 40 mg ew vs 40 mg eow achieved clinical remission at week 52 (maintenance primary end point; P = .069). In the integrated (main + Japan) population, 41.1% vs 30.1% of week-8 responders receiving 40 mg ew vs 40 mg eow achieved clinical remission at week 52 (nominal P = .045). Safety profiles were comparable between dosing regimens.
CONCLUSION
Although primary end points were not met, a >10% absolute difference in clinical remission was demonstrated with higher adalimumab maintenance dosing. Higher dosing regimens were generally well tolerated and consistent with the known safety profile of adalimumab in ulcerative colitis.
CLINICALTRIALS
gov, Number: NCT002209456.

Identifiants

pubmed: 35227777
pii: S0016-5085(22)00199-8
doi: 10.1053/j.gastro.2022.02.033
pii:
doi:

Substances chimiques

Adalimumab FYS6T7F842

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1891-1910

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Julián Panés (J)

Hospital Clinic de Barcelona, August Pi i Sunyer Biomedical Research Institute, Biomedical Research Networking Center in Hepatic and Digestive Diseases, Barcelona, Spain. Electronic address: jpanes@clinic.cat.

Jean-Frederic Colombel (JF)

Icahn School of Medicine at Mt Sinai, New York, New York.

Geert R D'Haens (GR)

Amsterdam Gastroenterology Endocrinology Metabolism and Gastroenterology and Hepatology Departments, Amsterdam University Medical Centers, Amsterdam, the Netherlands.

Stefan Schreiber (S)

Department of Internal Medicine, University Hospital Schleswig-Holstein, Kiel University, Kiel, Germany.

Remo Panaccione (R)

Department of Medicine, University of Calgary, Calgary, Alberta, Canada.

Laurent Peyrin-Biroulet (L)

Department of Gastroenterology, Centre Hospitalier Régional Universitaire de Nancy, Nutrition-Genetics and Exposure to Environmental Risks, Institut National de la Santé et de la Recherche Médicale, University of Lorraine, Nancy, France.

Edward V Loftus (EV)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Silvio Danese (S)

Gastroenterology and Endoscopy, Istituto di Ricovero e Cura a Carattere Scientifico, Ospedale San Raffaele and University Vita-Salute San Raffaele, Milan, Italy.

Satoshi Tanida (S)

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.

Yusuke Okuyama (Y)

Department of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan.

Edouard Louis (E)

Department of Gastroenterology, University Hospital Centre Hospitalier Universitaire de Liège, Liège, Belgium.

Alessandro Armuzzi (A)

Inflammatory Bowel Diseases Unit, Fondazione Policlinico Universitario A. Gemelli Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy.

Marc Ferrante (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Katholieke Universiteit Leuven, Leuven, Belgium.

Harald Vogelsang (H)

Medical University of Vienna, Vienna, Austria.

Toshifumi Hibi (T)

Center for Advanced Inflammatory Bowel Disease Research and Treatment, Kitasato University, Kitasato Institute Hospital, Tokyo, Japan.

Mamoru Watanabe (M)

Advanced Research Institute and Department of Gastroenterology and Hepatology, Tokyo Medical and Dental University, Tokyo, Japan.

Jessica Lefebvre (J)

AbbVie Inc, North Chicago, Illinois.

Tricia Finney-Hayward (T)

AbbVie Ltd, Maidenhead, Berkshire, England, United Kingdom.

Yuri Sanchez Gonzalez (Y)

AbbVie Inc, North Chicago, Illinois.

Thao T Doan (TT)

AbbVie Inc, North Chicago, Illinois.

Nael M Mostafa (NM)

AbbVie Inc, North Chicago, Illinois.

Kimitoshi Ikeda (K)

AbbVie GK, Minato-ku, Tokyo, Japan.

Wangang Xie (W)

AbbVie Inc, North Chicago, Illinois.

Bidan Huang (B)

AbbVie Inc, North Chicago, Illinois.

Joel Petersson (J)

AbbVie Inc, North Chicago, Illinois.

Jasmina Kalabic (J)

AbbVie Deutschland GmbH & Co KG, Ludwigshafen, Germany.

Anne M Robinson (AM)

AbbVie Inc, North Chicago, Illinois.

William J Sandborn (WJ)

Gastroenterology Department, University of California San Diego, La Jolla, California.

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