Outcome of Pregnancies in Female Patients With Inflammatory Bowel Diseases Treated With Vedolizumab.


Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
01 Jan 2019
Historique:
pubmed: 4 10 2018
medline: 15 5 2019
entrez: 4 10 2018
Statut: ppublish

Résumé

Vedolizumab is an IgG1 anti-α4β7 integrin antibody approved for the treatment of inflammatory bowel diseases [IBD], but without clear safety data during conception, pregnancy and nursing. Animal studies showed that mucosal vascular addressin cell adhesion molecule 1 [MAdCAM-1] is expressed by maternal vessels in the placenta and recruits α4β7-expressing cells that are considered important for maternal/fetal tolerance. Blocking this interaction by vedolizumab might affect this process. We aimed to evaluate pregnancy outcomes in vedolizumab-treated female IBD patients. We conducted a retrospective, multicentre Belgian observational study. Details on disease activity, prenatal complications, delivery and neonatal outcome were collected through a case report form. Twenty-four pregnancies were reported. Five women had active disease at conception and one patient flared during pregnancy. There were 23 live births. Complications were observed in 25% of pregnancies [premature rupture of membranes, pre-eclampsia, miscarriage, elective termination and stillbirth] and in 35% of infants [prematurity, intra-uterine growth retardation, small for gestational age and congenital malformations including hip dysplasia, pulmonary valve stenosis and Hirschprung's disease]. Vedolizumab was continued throughout pregnancy in two females and stopped in the 1st and 2nd trimester in five and 16 patients, respectively. For live born children, the median [interquartile range] gestational age, weight and Apgar score 5 min after birth were 39 [37-39.6] weeks, 3270 [3080-3585] grams and 10 [9-10], respectively. Although several complications were observed, both in mothers and in newborns, no firm conclusions can be drawn. Awaiting prospective and controlled registries, vigilance and strict follow-up of pregnant patients treated with vedolizumab seems mandatory.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Vedolizumab is an IgG1 anti-α4β7 integrin antibody approved for the treatment of inflammatory bowel diseases [IBD], but without clear safety data during conception, pregnancy and nursing. Animal studies showed that mucosal vascular addressin cell adhesion molecule 1 [MAdCAM-1] is expressed by maternal vessels in the placenta and recruits α4β7-expressing cells that are considered important for maternal/fetal tolerance. Blocking this interaction by vedolizumab might affect this process. We aimed to evaluate pregnancy outcomes in vedolizumab-treated female IBD patients.
METHODS METHODS
We conducted a retrospective, multicentre Belgian observational study. Details on disease activity, prenatal complications, delivery and neonatal outcome were collected through a case report form.
RESULTS RESULTS
Twenty-four pregnancies were reported. Five women had active disease at conception and one patient flared during pregnancy. There were 23 live births. Complications were observed in 25% of pregnancies [premature rupture of membranes, pre-eclampsia, miscarriage, elective termination and stillbirth] and in 35% of infants [prematurity, intra-uterine growth retardation, small for gestational age and congenital malformations including hip dysplasia, pulmonary valve stenosis and Hirschprung's disease]. Vedolizumab was continued throughout pregnancy in two females and stopped in the 1st and 2nd trimester in five and 16 patients, respectively. For live born children, the median [interquartile range] gestational age, weight and Apgar score 5 min after birth were 39 [37-39.6] weeks, 3270 [3080-3585] grams and 10 [9-10], respectively.
CONCLUSIONS CONCLUSIONS
Although several complications were observed, both in mothers and in newborns, no firm conclusions can be drawn. Awaiting prospective and controlled registries, vigilance and strict follow-up of pregnant patients treated with vedolizumab seems mandatory.

Identifiants

pubmed: 30281093
pii: 5114379
doi: 10.1093/ecco-jcc/jjy142
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Gastrointestinal Agents 0
vedolizumab 9RV78Q2002

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

12-18

Auteurs

Annick Moens (A)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.

Karen van Hoeve (K)

Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.
Department of Paediatric Gastroenterology, University Hospitals Leuven, KU Leuven, Leuven, Belgium.

Evelien Humblet (E)

Department of Gastroenterology, Ziekenhuis Oost-Limburg - Campus Sint-Jan, Genk, Belgium.

Jean-François Rahier (JF)

Deparment of Gastroenterology, CHU UCL Namur, Université catholique de Louvain, Yvoir, Belgium.

Peter Bossuyt (P)

Department of Gastroenterology, Imeldaziekenhuis, Bonheiden, Belgium.

Sophie Dewit (S)

Department of Gastroenterology, Mariaziekenhuis Noord-Limburg, Overpelt, Belgium.

Denis Franchimont (D)

Department of Gastroenterology, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.

Elisabeth Macken (E)

Department of Gastroenterology, Universiteit ziekenhuis Antwerpen, UZA, Antwerp, Belgium.

Jochen Nijs (J)

Department of Gastroenterology, Sint-Trudo Ziekenhuis, Sint-Truiden, Belgium.

Annelies Posen (A)

Department of Gastroenterology, AZ Vesalius, Tongeren, Belgium.

Beatrijs Strubbe (B)

Department of Gastroenterology, AZ Sint-Lucas, Gent, Belgium.

Anneleen Van Hootegem (A)

Department of Gastroenterology, AZ Klina, Brasschaat, Belgium.

Wouter Van Moerkercke (W)

Department of Gastroenterology, AZ Groeninge, Kortrijk, Belgium.

Séverine Vermeire (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.

Marc Ferrante (M)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, Leuven, Belgium.
Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, Belgium.

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Classifications MeSH