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Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review
A cystic fibrosis (CF) transmembrane conductor regulator (CFTR) gene modulating triple therapy combining elexacaftor-tezacaftor-ivacaftor (Trikafta) has been recently discovered. Its approval by the Food and Drug Administration (FDA) in 2019 has expanded the target therapy group to individuals aged...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583755/ https://www.ncbi.nlm.nih.gov/pubmed/36284811 http://dx.doi.org/10.7759/cureus.29359 |
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author | Dawood, Sarah N Rabih, Ahmad M Niaj, Ahmad Raman, Aishwarya Uprety, Manish Calero, Maria Jose Villanueva, Maria Resah B Joshaghani, Narges Villa, Nicole Badla, Omar Goit, Raman Saddik, Samia E Mohammed, Lubna |
author_facet | Dawood, Sarah N Rabih, Ahmad M Niaj, Ahmad Raman, Aishwarya Uprety, Manish Calero, Maria Jose Villanueva, Maria Resah B Joshaghani, Narges Villa, Nicole Badla, Omar Goit, Raman Saddik, Samia E Mohammed, Lubna |
author_sort | Dawood, Sarah N |
collection | PubMed |
description | A cystic fibrosis (CF) transmembrane conductor regulator (CFTR) gene modulating triple therapy combining elexacaftor-tezacaftor-ivacaftor (Trikafta) has been recently discovered. Its approval by the Food and Drug Administration (FDA) in 2019 has expanded the target therapy group to individuals aged twelve and up with at least one Phe508del (phenylalanine 508 deletion) mutation in the CFTR gene. This systematic review aims to assess this combination therapy's safety and efficacy. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines, an in-depth search was performed. The search was done by utilizing databases such as PubMed Central (PMC), Google Scholar, and Science Direct for articles related to this topic. Studies published in the last five years in the English language were chosen preliminarily. Further eligibility criteria and quality assessment tools were employed to assess the risk of bias and finalize ten articles to be used in this review. The chosen articles constituted four randomized control trials (RCTs), four systematic reviews, and two narrative reviews. The last date for data collection was April 24, 2022. Based on the findings of this review, we concluded that by combining three CFTR modulators, this therapy had outperformed all the currently available medications in terms of improving pulmonary function, reducing exacerbations, and enhancing the quality of life of CF patients. In clinical trials, headache and rash were the most common side effects, and laboratory testing to assess liver function is suggested. Long-term safety and effectiveness must be confirmed by the continued review of real-life patient data. Studies done on triple therapy thus far have been promising. Unfortunately, a small proportion of the CF population remains ineligible for any form of CFTR modulator therapy owing to their type of genetic mutation, and this provides ground for further research in this field. |
format | Online Article Text |
id | pubmed-9583755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-95837552022-10-24 Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review Dawood, Sarah N Rabih, Ahmad M Niaj, Ahmad Raman, Aishwarya Uprety, Manish Calero, Maria Jose Villanueva, Maria Resah B Joshaghani, Narges Villa, Nicole Badla, Omar Goit, Raman Saddik, Samia E Mohammed, Lubna Cureus Internal Medicine A cystic fibrosis (CF) transmembrane conductor regulator (CFTR) gene modulating triple therapy combining elexacaftor-tezacaftor-ivacaftor (Trikafta) has been recently discovered. Its approval by the Food and Drug Administration (FDA) in 2019 has expanded the target therapy group to individuals aged twelve and up with at least one Phe508del (phenylalanine 508 deletion) mutation in the CFTR gene. This systematic review aims to assess this combination therapy's safety and efficacy. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines, an in-depth search was performed. The search was done by utilizing databases such as PubMed Central (PMC), Google Scholar, and Science Direct for articles related to this topic. Studies published in the last five years in the English language were chosen preliminarily. Further eligibility criteria and quality assessment tools were employed to assess the risk of bias and finalize ten articles to be used in this review. The chosen articles constituted four randomized control trials (RCTs), four systematic reviews, and two narrative reviews. The last date for data collection was April 24, 2022. Based on the findings of this review, we concluded that by combining three CFTR modulators, this therapy had outperformed all the currently available medications in terms of improving pulmonary function, reducing exacerbations, and enhancing the quality of life of CF patients. In clinical trials, headache and rash were the most common side effects, and laboratory testing to assess liver function is suggested. Long-term safety and effectiveness must be confirmed by the continued review of real-life patient data. Studies done on triple therapy thus far have been promising. Unfortunately, a small proportion of the CF population remains ineligible for any form of CFTR modulator therapy owing to their type of genetic mutation, and this provides ground for further research in this field. Cureus 2022-09-20 /pmc/articles/PMC9583755/ /pubmed/36284811 http://dx.doi.org/10.7759/cureus.29359 Text en Copyright © 2022, Dawood et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Internal Medicine Dawood, Sarah N Rabih, Ahmad M Niaj, Ahmad Raman, Aishwarya Uprety, Manish Calero, Maria Jose Villanueva, Maria Resah B Joshaghani, Narges Villa, Nicole Badla, Omar Goit, Raman Saddik, Samia E Mohammed, Lubna Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review |
title | Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review |
title_full | Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review |
title_fullStr | Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review |
title_full_unstemmed | Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review |
title_short | Newly Discovered Cutting-Edge Triple Combination Cystic Fibrosis Therapy: A Systematic Review |
title_sort | newly discovered cutting-edge triple combination cystic fibrosis therapy: a systematic review |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583755/ https://www.ncbi.nlm.nih.gov/pubmed/36284811 http://dx.doi.org/10.7759/cureus.29359 |
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