Litcius/Paper detail

Reported congenital malformations after exposure to non‐tumour necrosis factor inhibitor biologics: A retrospective comparative study in EudraVigilance

Nafise Ghalandari, H. J. M. J. Crijns, Jorieke E. H. Bergman, Radboud J. E. M. Dolhain, Eugène van Puijenbroek, Johanna M. W. Hazes

2022British Journal of Clinical Pharmacology23 citationsDOIOpen Access PDF

Abstract

AIMS: To evaluate the number and nature of reported congenital malformations (CMs) after intrauterine exposure to non-tumour necrosis factor inhibitor biologics (non-TNFi biologics) compared to certolizumab pegol (CZP). METHODS: A retrospective comparative study was conducted in the EudraVigilance (EV) database. A safe biologic (CZP) was considered as the reference group. Odds ratios (ORs) for CMs were calculated for each non-TNFi biologic (including abatacept, anakinra, belimumab, ixekizumab, rituximab, secukinumab, tocilizumab, ustekinumab and vedolizumab), versus CZP (quantitative assessment). Then, CM patterns were reviewed in consultation with a clinical geneticist (qualitative assessment). RESULTS: ORs were not statistically significant except for belimumab and vedolizumab (similar in magnitude). Except for vedolizumab, no specific CM patterns were observed for the included non-TNFi biologics. Three cases of corpus callosum agenesis (CCA) were identified for vedolizumab (versus none in CZP and other investigated non-TNFi biologics). Two of the CCA cases were associated with other neurological CMs (one cerebral ventriculomegaly with microcephaly and one polymicrogyria). This may indicate that these CCAs are related to undiagnosed genetic alterations or are associated with the underlying maternal disease, although a definite relationship with vedolizumab exposure cannot be ruled out. CONCLUSION: No special safety signal was identified regarding the occurrence of CMs after exposure to abatacept (n = 64), anakinra (n = 20), belimumab (n = 93), ixekizumab (n = 29), rituximab (n = 57), secukinumab (n = 128), tocilizumab (n = 124) and ustekinumab (n = 215). Regarding observed CCAs in the vedolizumab group (n = 113), no firm conclusions can be made based on available information.

Topics & Concepts

MedicineVedolizumabAnakinraCertolizumab pegolTocilizumabSecukinumabBelimumabAbataceptInternal medicineRituximabUstekinumabPediatricsAdalimumabImmunologyInflammatory bowel diseaseB-cell activating factorArthritisTumor necrosis factor alphaDiseasePsoriatic arthritisLymphomaAntibodyB cellFolate and B Vitamins ResearchFetal and Pediatric Neurological DisordersImmunodeficiency and Autoimmune Disorders