Ustekinumab for Perianal Crohn's Disease: The BioLAP Multicenter Study From the GETAID.


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:
11 2020
Historique:
entrez: 6 11 2020
pubmed: 7 11 2020
medline: 15 12 2020
Statut: ppublish

Résumé

New therapeutic options for patients with Crohn's disease (CD) with perianal lesions failing anti-tumor necrosis factor (TNF) agents are needed. We aimed to assess the effectiveness of ustekinumab in perianal CD (pCD) and predictors of clinical success in a real-life multicenter cohort. We conducted a national multicenter retrospective cohort study in patients with either active or inactive pCD who received ustekinumab. In patients with active pCD at treatment initiation, the success of ustekinumab was defined by clinical success at 6 months assessed by the physician's judgment without additional medical or surgical treatment for pCD. Univariate and multivariable logistic regression analyses were performed to identify predictors of success. In patients with inactive pCD at ustekinumab initiation, the pCD recurrence-free survival was calculated using the Kaplan-Meier method. Two hundred seven patients were included, the mean age was 37.7 years, the mean duration of CD was 14.3 years, and the mean number of prior perianal surgeries was 2.8. Two hundred five (99%) patients had previously been exposed to at least 1 anti-TNF and 58 (28%) to vedolizumab. The median follow-up time was 48 weeks; 56/207 (27%) patients discontinued therapy after a median time of 43 weeks. In patients with active pCD, success was reached in 57/148 (38.5%) patients. Among patients with setons at initiation, 29/88 (33%) had a successful removal. The absence of optimization was associated with treatment success (P = 0.044, odds ratio 2.74; 95% confidence interval: 0.96-7.82). In multivariable analysis, the number of prior anti-TNF agents (≥3) was borderline significant (P = 0.056, odds ratio 0.4; 95% confidence interval: 0.15-1.08). In patients with inactive pCD at initiation, the probability of recurrence-free survival was 86.2% and 75.1% at weeks 26 and 52, respectively. Ustekinumab appears as a potential effective therapeutic option in perianal refractory CD. Further prospective studies are warranted.

Identifiants

pubmed: 33156100
doi: 10.14309/ajg.0000000000000810
pii: 00000434-202011000-00016
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Antibodies, Monoclonal, Humanized 0
Gastrointestinal Agents 0
Tumor Necrosis Factor Inhibitors 0
vedolizumab 9RV78Q2002
Ustekinumab FU77B4U5Z0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1812-1820

Références

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Auteurs

Constance Chapuis-Biron (C)

Department of Gastroenterology, University Hospital of Besançon, University Bourgogne Franche-Comté, Besançon, France.

Julien Kirchgesner (J)

Department of Gastroenterology, Saint-Antoine Hospital, Assitance Publique-Hôpitaux de Paris (AP-HP), Paris, France.

Benjamin Pariente (B)

Department of Hepatogastroenterology, University Hospital of Lille, Lille, France.

Yoram Bouhnik (Y)

Department of Gastroenterology, AP-HP, Hôpital Beaujon, Paris, France.

Aurélien Amiot (A)

Department of Gastroenterology, AP-HP, Hôpital Henri-Mondor, Paris, France.

Stéphanie Viennot (S)

Department of Hepatogastroenterology, University Hospital of Caen, Caen, France.

Mélanie Serrero (M)

Department of Gastroenterology, AP-HM, Hôpital Nord, Marseille, France.

Mathurin Fumery (M)

Department of Hepatogastroenterology, Peritox, University Hospital of Amiens, Amiens, France.

Matthieu Allez (M)

Department of Gastroenterology, AP-HP, Hôpital Saint Louis, Paris, France.

Laurent Siproudhis (L)

Department of Hepatogastroenterology, CHU Pontchaillou, University Hospital of Rennes, Rennes, France.

Anthony Buisson (A)

Department of Hepatogastroenterology, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.

Guillaume Pineton de Chambrun (G)

Department of Hepatogastroenterology, University Hospital of Montpellier, Montpellier, France.

Vered Abitbol (V)

Department of Gastroenterology, AP-HP, Hôpital Cochin, Paris, France.

Stéphane Nancey (S)

Department of Gastroenterology, Hospices Civils de Lyon, Lyon Sud Hospital, Lyon, France.

Ludovic Caillo (L)

Department of Hepatogastroenterology, University Hospital of Nimes, Nimes, France.

Laurianne Plastaras (L)

Department of Hepatogastroenterology, Hospital Pasteur, Colmar, France.

Guillaume Savoye (G)

Department of Hepatogastroenterology, University Hospital of Rouen.

Elise Chanteloup (E)

Department of Gastroenterology, Hôpital Paris Saint Joseph, Paris, France.

Marion Simon (M)

Department of Gastroenterology, Institut Mutualiste Montsouris, Paris, France.

Nina Dib (N)

Department of Hepatogastroenterology, University Hospital of Angers, Angers, France.

Sylvie Rajca (S)

Department of Gastroenterology, AP-HP, Hôpital Louis-Mourier, Paris, France.

Morgane Amil (M)

Department of Hepatogastroenterology, Centre hospitalier La Roche-sur-Yon, La Roche-sur-Yon, France.

Anne-Laure Parmentier (AL)

Department of Methodology, University Hospital of Besançon, Besançon, France.

Laurent Peyrin-Biroulet (L)

Department of Gastroenterology, Inserm U954, University Hospital of Nancy, Lorraine University, Nancy, France.

Lucine Vuitton (L)

Department of Gastroenterology, University Hospital of Besançon, University Bourgogne Franche-Comté, Besançon, France.

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