Caution advised in the use of CFTR modulator treatment for individuals harboring specific CFTR variants.

CFTR modulator CFTR variant Clinical outcomes Non CF-causing variant Variant interpretation

Journal

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Titre abrégé: J Cyst Fibros
Pays: Netherlands
ID NLM: 101128966

Informations de publication

Date de publication:
09 2022
Historique:
received: 11 12 2021
revised: 09 03 2022
accepted: 24 04 2022
pubmed: 9 5 2022
medline: 28 9 2022
entrez: 8 5 2022
Statut: ppublish

Résumé

In December 2020, the U.S. Food and Drug Administration (FDA) expanded the list of CFTR variants approved for treatment with CFTR modulators drugs from 39 to 183. Clinicians should be aware that individuals harboring certain variants approved for treatment may not respond to or benefit from this therapy. After review, the expert panel leading the CFTR2 project identified four categories of variants that may not result in a clinical response to modulator treatment: 15 variants assigned as non CF-causing; 45 variants of unknown significance; six variants known or suspected to cause mis-splicing as their primary defect rather than an amino acid substitution; and eight variants known to occur together in cis with another deleterious variant not expected to lead to CFTR protein (nonsense or frameshift). The potential risks and benefits of CFTR modulator therapy should be considered carefully for individuals harboring these variants.

Identifiants

pubmed: 35527187
pii: S1569-1993(22)00108-4
doi: 10.1016/j.jcf.2022.04.019
pii:
doi:

Substances chimiques

CFTR protein, human 0
Cystic Fibrosis Transmembrane Conductance Regulator 126880-72-6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

856-860

Informations de copyright

Copyright © 2022. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest CC serves on advisory boards for Vertex Pharmaceuticals, Mylan, Chiesi Farmaceutici, and Actelion. GRC served as a consultant for Vertex Pharmaceuticals and has a relative employed by Vertex Pharmaceuticals. All other authors report none.

Auteurs

Karen S Raraigh (KS)

McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.

Michelle H Lewis (MH)

Berman Institute of Bioethics, Johns Hopkins University, Baltimore, MD 21287, United States.

Joseph M Collaco (JM)

Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.

Mary Corey (M)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.

Christopher M Penland (CM)

Cystic Fibrosis Foundation, Bethesda, MD 20814, United States.

Anne L Stephenson (AL)

Department of Respirology, Adult Cystic Fibrosis Program, St. Michael's Hospital, Toronto, Ontario, Canada.

Johanna M Rommens (JM)

Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.

Carlo Castellani (C)

IRCCS Istituto Giannina Gaslini, Cystic Fibrosis Center, Genoa, Italy.

Garry R Cutting (GR)

McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States. Electronic address: gcutting@jhmi.edu.

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Classifications MeSH