Safety of ustekinumab or vedolizumab in pregnant inflammatory bowel disease patients: a multicentre cohort study.


Journal

Alimentary pharmacology & therapeutics
ISSN: 1365-2036
Titre abrégé: Aliment Pharmacol Ther
Pays: England
ID NLM: 8707234

Informations de publication

Date de publication:
02 2021
Historique:
received: 22 05 2020
revised: 23 06 2020
accepted: 14 11 2020
pubmed: 22 12 2020
medline: 6 3 2021
entrez: 21 12 2020
Statut: ppublish

Résumé

The prevalence of inflammatory bowel diseases (IBD) is high in women of childbearing age. Achieving clinical remission from conception to delivery using current medications is a major issue in IBD. To assess maternal and neonatal complications and management of vedolizumab or ustekinumab) in pregnant women with IBD receiving these agents. We performed a retrospective cohort study among GETAID centres including women with IBD who received ustekinumab or vedolizumab during pregnancy or within the 2 months before conception and compared outcomes to women exposed to anti-TNF treatment during pregnancy. Seventy-three pregnancies in 68 women with IBD were analysed: 29 on ustekinumab resulting in 26 (90%) live births, two (7%) spontaneous abortions and one (3%) elective termination; 44 on vedolizumab resulting in 38 (86%) live births, five (11%) spontaneous abortions and one (3%) medical interruption. The control group included 88 pregnancies exposed to anti-TNF in 76 women with IBD. The median age at conception, the proportion of women who smoked or in clinical activity at conception was comparable between groups. Only the proportion of patients exposed to >2 anti-TNF agents was significantly increased among the ustekinumab and vedolizumab groups compared to control group (22% and 10% vs 3%, P < 0.005). Rates of prematurity, spontaneous abortion, congenital malformations and maternal complications were comparable between groups. We report 73 pregnancies in patients receiving vedolizumab or ustekinumab without a negative signal on maternal or neonatal outcomes. Further prospective studies are needed on the outcomes of pregnancies with new biologic drugs.

Sections du résumé

BACKGROUND
The prevalence of inflammatory bowel diseases (IBD) is high in women of childbearing age. Achieving clinical remission from conception to delivery using current medications is a major issue in IBD.
AIMS
To assess maternal and neonatal complications and management of vedolizumab or ustekinumab) in pregnant women with IBD receiving these agents.
METHODS
We performed a retrospective cohort study among GETAID centres including women with IBD who received ustekinumab or vedolizumab during pregnancy or within the 2 months before conception and compared outcomes to women exposed to anti-TNF treatment during pregnancy.
RESULTS
Seventy-three pregnancies in 68 women with IBD were analysed: 29 on ustekinumab resulting in 26 (90%) live births, two (7%) spontaneous abortions and one (3%) elective termination; 44 on vedolizumab resulting in 38 (86%) live births, five (11%) spontaneous abortions and one (3%) medical interruption. The control group included 88 pregnancies exposed to anti-TNF in 76 women with IBD. The median age at conception, the proportion of women who smoked or in clinical activity at conception was comparable between groups. Only the proportion of patients exposed to >2 anti-TNF agents was significantly increased among the ustekinumab and vedolizumab groups compared to control group (22% and 10% vs 3%, P < 0.005). Rates of prematurity, spontaneous abortion, congenital malformations and maternal complications were comparable between groups.
CONCLUSION
We report 73 pregnancies in patients receiving vedolizumab or ustekinumab without a negative signal on maternal or neonatal outcomes. Further prospective studies are needed on the outcomes of pregnancies with new biologic drugs.

Identifiants

pubmed: 33345331
doi: 10.1111/apt.16192
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Tumor Necrosis Factor-alpha 0
vedolizumab 9RV78Q2002
Ustekinumab FU77B4U5Z0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

460-470

Investigateurs

Benjamin Pariente (B)
Maria Nachury (M)
Pauline Wils (P)
Pierre Desreumaux (P)
Julien Branche (J)
Romain Gérard (R)
Philippe Seksik (P)
Anne Bourrier (A)
Laurent Beaugerie (L)
Harry Sokol (H)
Julien Kirchgesner (J)
Carmen Stefanescu (C)
Yoram Bouhnik (Y)
Xavier Treton (X)
Stephane Nancey (S)
Gilles Boschetti (G)
Bernard Flourié (B)
Claire Gay (C)
Pauline Danion (P)
Chloe Venturin (C)
Matthieu Allez (M)
Jean-Marc Gornet (JM)
Clotilde Baudry (C)
Guillaume Pineton de Chambrun (G)
Romain Altwegg (R)
Cyrielle Gilletta (C)
Lucine Vuitton (L)
Stephanie Viennot (S)
Melanie Serrero (M)
Jean Charles Grimaud (JC)
Mathurin Fumery (M)
Franck Brazier (F)
Clara Yzet (C)
Michael Collins (M)
Félix Goutorbe (F)
Hedia Brixi (H)
Guillaume Cadiot (G)
Guillaume Bouguen (G)
Noémie Tavernier (N)
Médina Boualit (M)
Aurélien Amiot (A)
Charlotte Gagnière (C)
Jenny Tannoury (J)
Vered Abitbol (V)
David Laharie (D)
Pauline Rivière (P)
Florian Poullenot (F)

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

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