Exposure to CFTR Modulators During Pregnancy in Cystic Fibrosis: Four Cases to Highlight Neonatal Diagnostic Challenges and Outcomes

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Authors: Louis Domenach, Adrien Pagin, Camille Cisterne, Marie‐Pierre Audrézet, L. Couderc, Laetitia Monteil, Léa Roditis, Marlène Murris, Julie Macey, Michael John Fayon, S. Bui, Marie‐Pierre Reboul
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Abstract

CFTR modulators have transformed the clinical evolution of patients with CF. The number of pregnancies is increasing in women with CF, most of whom are now treated with CFTR modulators such as elexacaftor/tezacaftor/ivacaftor (ETI) or Tezacaftor/Ivacaftor. This raises some questions as we still lack data on foetal and maternal safety. The preliminary data seem to support the continuation of modulators. Some of these mothers may also give birth to newborns with CF and this raises more questions. We report here four cases of CF newborns whose mothers were treated with CFTR modulators throughout pregnancy to help refine potential foetal outcomes of in utero administration of CF modulators. No maternal or foetal complications could be attributed to CFTR modulators. Three CF newborns were exposed to ETI and were false negative of the newborn screening. Two of them were pancreatic sufficient at birth. The remaining patient, exposed to Tezacaftor/Ivacaftor (TI) alone, showed elevated immunoreactive trypsin (IRT) and severe pancreatic insufficiency at birth. These cases highlight that in utero administration of ETI could potentially improve neonatal outcomes of CF newborns and cause newborn screening false negative.

Fields of Study & Subjects

Cystic Fibrosis Research Advances Pregnancy and Medication Impact Lysosomal Storage Disorders Research

Publication details

Journal / source
International Journal of Neonatal Screening
Volume
12
Issue
1
Pages
11–11
Publication date
26 February 2026
Language
EN