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Caution advised in the use of CFTR modulator treatment for individuals harboring specific CFTR variants.
Raraigh, Karen S; Lewis, Michelle H; Collaco, Joseph M; Corey, Mary; Penland, Christopher M; Stephenson, Anne L; Rommens, Johanna M; Castellani, Carlo; Cutting, Garry R.
Afiliação
  • Raraigh KS; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
  • Lewis MH; Berman Institute of Bioethics, Johns Hopkins University, Baltimore, MD 21287, United States.
  • Collaco JM; Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.
  • Corey M; Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Penland CM; Cystic Fibrosis Foundation, Bethesda, MD 20814, United States.
  • Stephenson AL; Department of Respirology, Adult Cystic Fibrosis Program, St. Michael's Hospital, Toronto, Ontario, Canada.
  • Rommens JM; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Castellani C; IRCCS Istituto Giannina Gaslini, Cystic Fibrosis Center, Genoa, Italy.
  • Cutting GR; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States. Electronic address: gcutting@jhmi.edu.
J Cyst Fibros ; 21(5): 856-860, 2022 09.
Article em En | MEDLINE | ID: mdl-35527187
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article