Real-world assessment of LCI following lumacaftor-ivacaftor initiation in adolescents and adults with cystic fibrosis

被引:7
作者
Reix, Philippe [1 ,2 ]
Tatopoulos, Aurelie [3 ]
Ioan, Iulia [4 ]
Le Bourgeois, Muriel [5 ]
Bui, Stephanie [6 ,7 ]
Choukroun, Marie Luce [8 ]
Bessaci-Kabouya, Katia [9 ,10 ]
Gerardin, Michele [11 ]
Bokov, Plamen [12 ,13 ]
Da Silva, Jennifer [14 ,15 ,16 ]
Paillasseur, Jean-Louis [17 ]
Burgel, Pierre Regis [14 ,15 ,18 ,19 ]
机构
[1] Hosp Civils Lyon, Cyst Fibrosis Ctr, Lyon, France
[2] Univ Claude Bernard Lyon 1, UMR 5558, Equipe EMET, CNRS, Lyon, France
[3] CHU Nancy, Hop Enfants, Pediat Cyst Fibrosis Ctr, Nancy, France
[4] CHU Nancy, Hop Enfants, Serv Explorat Fonctionnelles Pediat, Nancy, France
[5] Hop Univ Necker Enfants Malad, Pediat Resp Dis & Cyst Fibrosis Ctr, Natl Reference Cyst Fibrosis Reference Ctr, Paris, France
[6] CHU Bordeaux, Pediat Resp Dis & Cyst Fibrosis Ctr, Bordeaux, France
[7] CHU Bordeaux, CIC 1401, Bordeaux, France
[8] CHU Bordeaux, Serv Explorat Fonctionnelles Resp Pediat, Bordeaux, France
[9] Amer Mem Hosp, Dept Pediat A, Reims, France
[10] Amer Mem Hosp, Cyst Fibrosis Ctr, Reims, France
[11] Hop Robert Debre, AP HP, Pediat Cyst Fibrosis Ctr, Paris, France
[12] Hop Robert Debre, AP HP, Serv Physiol Pediat, Paris, France
[13] Univ Paris, UMR1141, Equipe NeoPhen, INSERM Cotutelle, Paris, France
[14] Univ Paris, Paris U1016, Inst Cochin, INSERM, Paris, France
[15] ERN Lung CF Network, Paris, France
[16] Hop Cochin, AP HP, URC CIC Paris Descartes Necker Cochin, Paris, France
[17] Effi Stat, Paris, France
[18] Cochin Hosp, AP HP, Resp Med, Paris, France
[19] Cochin Hosp, AP HP, Natl Cyst Fibrosis Reference Ctr, Paris, France
关键词
Lumacaftor; CFTR modulators; Cystic fibrosis; Multiple breath washout; LUNG CLEARANCE INDEX; AGED; 6-11; YEARS;
D O I
10.1016/j.jcf.2021.06.002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Lung clearance index (LCI) is a biomarker of ventilation inhomogeneity. Data are scarce on its usefulness in daily practice for monitoring the effects of treatments in older children and adults with CF. In this French observational study of lumacaftor-ivacaftor, 63 of 845 patients (7.5%) had available LCI performed at baseline and at six (M6; n = 34) or 12 months (M12; n = 46) after lumacaftor-ivacaftor initiation. At inclusion, median [IQR] age was 16 years [13-17], ppFEV 1 was 72.8 [59.6-80.7], and LCI was 12.3 [10.315.0]. At both M6 and M12, no statistically significant LCI increases of 0.13 units or 1.34% (95% CI: 4.85-7.53) and 0.6 units or 6.66% (95% CI: -0.03-13.5) were observed. Discordant results between LCI and ppFEV 1 were observed in one-third of the patients. In daily practice, LCI monitoring in adolescents and young adults with moderate lung disease gives results that are more heterogenous than those reported in children with milder disease.
引用
收藏
页码:155 / 159
页数:5
相关论文
共 50 条
  • [41] Effectiveness of lumacaftor/ivacaftor initiation in children with cystic fibrosis aged 2 through 5 years on disease progression: Interim results from an ongoing registry-based study
    Kim, Claire
    Higgins, Mark
    Liu, Lingyun
    Volkova, Nataliya
    Zolin, Anna
    Naehrlich, Lutz
    JOURNAL OF CYSTIC FIBROSIS, 2024, 23 (03) : 436 - 442
  • [42] Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells
    Favia, Maria
    Gallo, Crescenzio
    Guerra, Lorenzo
    De Venuto, Domenica
    Diana, Anna
    Polizzi, Angela Maria
    Montemurro, Pasqualina
    Mariggio, Maria Addolorata
    Leonetti, Giuseppina
    Manca, Antonio
    Casavola, Valeria
    Conese, Massimo
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (07)
  • [43] Real-world data confirm elexacftor/tezacaftor/ivacaftor modulators halves sweat chloride concentration in eligible people with cystic fibrosis
    Bryrup, Thomas
    Faurholt-Jepsen, Daniel
    Pressler, Tacjana
    Henriksen, Esben Herborg
    Leo-Hansen, Christian
    Nielsen, Bibi Uhre
    Hojte, Christine
    Mathiesen, Inger Hee Mabuza
    Katzenstein, Terese L.
    Jeppesen, Majbritt
    Jensen-Fangel, Soren
    Olesen, Hanne Vebert
    Skov, Marianne
    Qvist, Tavs
    Olsen, Mette Frahm
    APMIS, 2024, 132 (10) : 728 - 733
  • [44] Real life evaluation of the multi-organ effects of Lumacaftor/Ivacaftor on F508del homozygous cystic fibrosis patients
    Yaacoby-Bianu, Karin
    Schnapp, Zeev
    Koren, Ilana
    Ilivitzki, Anat
    Khatib, Mohamed
    Shorbaji, Nadeem
    Shteinberg, Michal
    Livnat, Galit
    BMC PHARMACOLOGY & TOXICOLOGY, 2022, 23 (01)
  • [45] Real life evaluation of the multi-organ effects of Lumacaftor/Ivacaftor on F508del homozygous cystic fibrosis patients
    Karin Yaacoby-Bianu
    Zeev Schnapp
    Ilana Koren
    Anat Ilivitzki
    Mohamed Khatib
    Nadeem Shorbaji
    Michal Shteinberg
    Galit Livnat
    BMC Pharmacology and Toxicology, 23
  • [46] Cystic fibrosis pathogens persist in the upper respiratory tract following initiation of elexacaftor/tezacaftor/ivacaftor therapy
    Hilliam, Yasmin
    Armbruster, Catherine R.
    Rapsinski, Glenn J.
    Marshall, Christopher W.
    Moore, John
    Koirala, Junu
    Krainz, Leah
    Gaston, Jordan R.
    Cooper, Vaughn S.
    Lee, Stella E.
    Bomberger, Jennifer M.
    MICROBIOLOGY SPECTRUM, 2024, 12 (08):
  • [47] Longitudinal improvements in clinical and functional outcomes following initiation of elexacaftor/tezacaftor/ivacaftor in patients with cystic fibrosis
    Vijaykumar, Kadambari
    Leung, Hui Min
    Barrios, Amilcar
    Wade, Justin
    Hathorne, Heather Y.
    Nichols, David P.
    Tearney, Guillermo J.
    Rowe, Steven M.
    Solomon, George M.
    HELIYON, 2024, 10 (08)
  • [48] Retrospective observational study of French patients with cystic fibrosis and a G1y551Asp-CFTR mutation after 1 and 2 years of treatment with ivacaftor in a real-world setting
    Hubert, Dominique
    Dehillotte, Clemence
    Munck, Anne
    David, Valerie
    Baek, Jinmi
    Mely, Laurent
    Dominique, Stephane
    Ramel, Sophie
    Boucher, Isabelle Danner
    Lefeuvre, Sylvaine
    Reynaud, Quitterie
    Colomb-Jung, Virginie
    Bakouboula, Prissile
    Lemonnier, Lydie
    JOURNAL OF CYSTIC FIBROSIS, 2018, 17 (01) : 89 - 95
  • [49] Clinical, economic, and societal burden of cystic fibrosis and the impact of the CFTR modulator, lumacaftor/ivacaftor: an assessment using linked registry data in Sweden
    Lindblad, Anders
    de Monestrol, Isabelle
    Gilljam, Marita
    Krantz, Christina
    McGarry, Lisa J.
    Banefelt, Jonas
    Aldven, Martina
    JOURNAL OF MEDICAL ECONOMICS, 2024, 27 (01) : 897 - 906
  • [50] First experience in Switzerland in Phe508del homozygous cystic fibrosis patients with end-stage pulmonary disease enrolled in a lumacaftor-ivacaftor therapy trial - preliminary results
    Christian, Murer
    Lars, Huber C.
    Thomas, Kurowski
    Astrid, Hirt
    Cecile, Robinson
    Urs, Buergi
    Christian, Benden
    SWISS MEDICAL WEEKLY, 2018, 148