Histologic Healing Rates of Medical Therapies for Ulcerative Colitis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.


Journal

The American journal of gastroenterology
ISSN: 1572-0241
Titre abrégé: Am J Gastroenterol
Pays: United States
ID NLM: 0421030

Informations de publication

Date de publication:
05 2019
Historique:
pubmed: 30 1 2019
medline: 17 1 2020
entrez: 30 1 2019
Statut: ppublish

Résumé

Histologic remission is a potentially valuable means of assessing disease activity and treatment response in ulcerative colitis (UC). However, the efficacy of existing therapies to achieve this outcome is unclear. We performed a systematic review and meta-analysis of histologic outcomes in UC randomized controlled trials and examined the relationship between histologic and endoscopic outcomes. MEDLINE, EMBASE, CENTRAL, and the Cochrane IBD Register were searched for randomized controlled trials of aminosalicylates, corticosteroids, immunosuppressives, biologics, and small molecules. Histologic and endoscopic remission and response data were independently extracted and pooled using binomial-normal random-effect or fixed-effect models. Pooled efficacy estimates were calculated as risk ratios (RRs) using the Mantel-Haenszel method. Univariable and multivariable random-effect meta-regression models examined factors associated with histologic remission. Seventy-four studies (68 induction and 7 maintenance) were identified. Topical aminosalicylate enemas [37.2%, 95% confidence interval (CI), 29.0-46.3] and suppositories (44.9%, 95% CI, 28.9-62.3) had the highest induction of histologic remission rates. Aminosalicylate enemas (RR = 4.14, 95% CI, 2.35-7.31), aminosalicylate suppositories (RR = 3.94, 95% CI, 1.26-12.32), and budesonide multimatrix (RR = 1.47, 95% CI 1.08-1.99) had higher histologic remission rates than placebo. Data were lacking for biologics and immunosuppressives. The pooled histologic remission rate for placebo in induction studies was 10.4% (95% CI, 7.1-15.2). Histologic and endoscopic remission correlated strongly (r = 0.66; 95% CI, 0.50-0.78). In multivariate analysis of placebo-arm data, less severe clinical disease activity and corticosteroid use were associated with higher histologic remission rates. Similarly, mild clinical disease activity was associated with higher histologic remission rates when active-arm data were analyzed. Histologic remission rates for current UC treatments ranged from 15.0% to 44.9% according to drug class and patient population with the highest rates observed for topical aminosalicylates. Placebo remission rates were low with relatively narrow CIs. These data provide benchmarks to inform future trial design. Histologic remission is a potential treatment target in clinical practice.

Identifiants

pubmed: 30694863
doi: 10.14309/ajg.0000000000000111
doi:

Substances chimiques

Gastrointestinal Agents 0

Types de publication

Journal Article Meta-Analysis Research Support, N.I.H., Extramural Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

733-745

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Robert Battat (R)

Division of Gastroenterology, University of California, San Diego, La Jolla, California, USA.
Robarts Clinical Trials Inc., London, Ontario, Canada.

Marjolijn Duijvestein (M)

Robarts Clinical Trials Inc., London, Ontario, Canada.
Academic Medical Center, Amsterdam, Netherlands.

Leonardo Guizzetti (L)

Robarts Clinical Trials Inc., London, Ontario, Canada.

Daksh Choudhary (D)

Department of Medicine, University of Western Ontario, London, Ontario, Canada.

Brigid S Boland (BS)

Division of Gastroenterology, University of California, San Diego, La Jolla, California, USA.

Parambir S Dulai (PS)

Division of Gastroenterology, University of California, San Diego, La Jolla, California, USA.

Claire E Parker (CE)

Robarts Clinical Trials Inc., London, Ontario, Canada.

Tran M Nguyen (TM)

Robarts Clinical Trials Inc., London, Ontario, Canada.

Siddharth Singh (S)

Division of Gastroenterology, University of California, San Diego, La Jolla, California, USA.

Niels Vande Casteele (N)

Division of Gastroenterology, University of California, San Diego, La Jolla, California, USA.
Robarts Clinical Trials Inc., London, Ontario, Canada.

Rish K Pai (RK)

Department of Pathology, Mayo Clinic Arizona, Scottsdale, Arizona, USA.

Brian G Feagan (BG)

Robarts Clinical Trials Inc., London, Ontario, Canada.
Department of Medicine, University of Western Ontario, London, Ontario, Canada.
Department of Epidemiology and Biostatistics, University of Western Ontario, London Ontario, Canada.

William J Sandborn (WJ)

Division of Gastroenterology, University of California, San Diego, La Jolla, California, USA.

Vipul Jairath (V)

Robarts Clinical Trials Inc., London, Ontario, Canada.
Department of Medicine, University of Western Ontario, London, Ontario, Canada.
Department of Epidemiology and Biostatistics, University of Western Ontario, London Ontario, Canada.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH