Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies Review

Cystic fibrosis is an autosomal recessive disease caused by structure abnormalities in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. It is characterized by severe course and poor prognosis without or with insufficient treatment. Approval of pathogenetic therapy medications, CF...

Full description

Saved in:
Bibliographic Details
Main Authors: Nataliya Yu. Kashirskaya, Nika V. Petrova, Rena A. Zinchenko
Format: Article
Language:English
Published: "Paediatrician" Publishers LLC 2021-12-01
Series:Вопросы современной педиатрии
Subjects:
Online Access:https://vsp.spr-journal.ru/jour/article/view/2794
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849411723547639808
author Nataliya Yu. Kashirskaya
Nika V. Petrova
Rena A. Zinchenko
author_facet Nataliya Yu. Kashirskaya
Nika V. Petrova
Rena A. Zinchenko
author_sort Nataliya Yu. Kashirskaya
collection DOAJ
description Cystic fibrosis is an autosomal recessive disease caused by structure abnormalities in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. It is characterized by severe course and poor prognosis without or with insufficient treatment. Approval of pathogenetic therapy medications, CFTR modulators (potentiators and correctors), for clinical use in 2012 in the United States has reduced mortality from this disease. This article provides the overview of studies on clinical efficacy and safety of ivacaftor/lumacaftor combination (Iva/Lum) — the first licensed CFTR modulator medication for homozygous patients with F508del variant. It was shown that Iva/Lum increases lung function, reduce the number of acute conditions of bronchopulmonary process (including those that require antibiotics and hospitalization), partially restores pancreas exocrine function, increases body weight and mass growth index, and improves quality of life. It allows considering it as favorable effect on the course and prognosis of cystic fibrosis. It was also noted that the early onset of the drug administration (from the age of two) positively affects the prognosis of the disease, increasing life expectancy and improving quality of life.
format Article
id doaj-art-7a6d41e347b04ef59ee80f7db41c520c
institution Kabale University
issn 1682-5527
1682-5535
language English
publishDate 2021-12-01
publisher "Paediatrician" Publishers LLC
record_format Article
series Вопросы современной педиатрии
spelling doaj-art-7a6d41e347b04ef59ee80f7db41c520c2025-08-20T03:34:41Zeng"Paediatrician" Publishers LLCВопросы современной педиатрии1682-55271682-55352021-12-01206s55856610.15690/vsp.v20i6S.23632001Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies ReviewNataliya Yu. Kashirskaya0Nika V. Petrova1Rena A. Zinchenko2Research Centre for Medical Genetics; Moscow Regional Research and Clinical InstituteResearch Centre for Medical GeneticsResearch Centre for Medical Genetics; N.A. Semashko National Research Institute of Public Health; Pirogov Russian National Research Medical UniversityCystic fibrosis is an autosomal recessive disease caused by structure abnormalities in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. It is characterized by severe course and poor prognosis without or with insufficient treatment. Approval of pathogenetic therapy medications, CFTR modulators (potentiators and correctors), for clinical use in 2012 in the United States has reduced mortality from this disease. This article provides the overview of studies on clinical efficacy and safety of ivacaftor/lumacaftor combination (Iva/Lum) — the first licensed CFTR modulator medication for homozygous patients with F508del variant. It was shown that Iva/Lum increases lung function, reduce the number of acute conditions of bronchopulmonary process (including those that require antibiotics and hospitalization), partially restores pancreas exocrine function, increases body weight and mass growth index, and improves quality of life. It allows considering it as favorable effect on the course and prognosis of cystic fibrosis. It was also noted that the early onset of the drug administration (from the age of two) positively affects the prognosis of the disease, increasing life expectancy and improving quality of life.https://vsp.spr-journal.ru/jour/article/view/2794cystic fibrosispathogenetic therapycftr modulatorsivacaftorlumacaftor
spellingShingle Nataliya Yu. Kashirskaya
Nika V. Petrova
Rena A. Zinchenko
Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies Review
Вопросы современной педиатрии
cystic fibrosis
pathogenetic therapy
cftr modulators
ivacaftor
lumacaftor
title Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies Review
title_full Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies Review
title_fullStr Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies Review
title_full_unstemmed Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies Review
title_short Clinical Efficacy and Safety of Ivacaftor/Lumacaftor Combination in Patients with Cystic Fibrosis: International Studies Review
title_sort clinical efficacy and safety of ivacaftor lumacaftor combination in patients with cystic fibrosis international studies review
topic cystic fibrosis
pathogenetic therapy
cftr modulators
ivacaftor
lumacaftor
url https://vsp.spr-journal.ru/jour/article/view/2794
work_keys_str_mv AT nataliyayukashirskaya clinicalefficacyandsafetyofivacaftorlumacaftorcombinationinpatientswithcysticfibrosisinternationalstudiesreview
AT nikavpetrova clinicalefficacyandsafetyofivacaftorlumacaftorcombinationinpatientswithcysticfibrosisinternationalstudiesreview
AT renaazinchenko clinicalefficacyandsafetyofivacaftorlumacaftorcombinationinpatientswithcysticfibrosisinternationalstudiesreview