Longitudinal effects of elexacaftor/tezacaftor/ivacaftor on liver tests at a large single adult cystic fibrosis centre

被引:22
|
作者
Tewkesbury, Daniel H. [1 ,2 ]
Athwal, Varinder [1 ,3 ]
Bright-Thomas, Rowland J. [1 ,2 ]
Jones, Andrew M. [1 ,2 ]
Barry, Peter J. [1 ,2 ,4 ]
机构
[1] Manchester Univ NHS Fdn Trust, Manchester, England
[2] Univ Manchester, Div Immunol Immun Infect & Resp Med, Manchester, England
[3] Univ Manchester, Div Diabet Endocrine & Gastroenterol, Manchester, England
[4] Wythenshawe Hosp, Manchester Adult Cyst Fibrosis Ctr, Southmoor Rd, Manchester M23 9LT, England
关键词
MANAGEMENT; IVACAFTOR;
D O I
10.1016/j.jcf.2023.01.007
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Elexacaftor/tezacaftor/ivacaftor (E/T/I) therapy has resulted in substantial improvements in health status for many with cystic fibrosis. Monitoring of liver tests is recommended due to observed rises in transaminases in trials and cases of hepatotoxicity. Comprehensive data in large populations of unselected individuals and those with established CF related liver disease (CFLD) is lacking. Methods: Patients prescribed E/T/I at a large, adult centre had liver tests monitored at least 3 monthly for 12 months. Changes in individual liver tests were analysed and abnormalities were compared in those with and without CFLD.Results: 255 of 267 eligible patients were included. Mild rises in median ALT, AST and bilirubin from baseline to 3 months (all p < 0.001) within normal limits were noted which were sustained. There were no differences in changes in liver tests between those with or without CFLD. There was a significant dif-ference in alkaline phosphatase for those with raised levels at baseline versus those with normal baseline level (-18.5 vs + 2.0 IU/L, p = 0.002). Clinically significant rises in ALT and AST occurred in 8 (3.1%) and 6 (2.4%) cases respectively, with derangements in 2 individuals attributed to therapy.Conclusions: E/T/I leads to a mild, likely clinically insignificant increase in ALT, AST and bilirubin after 3 months which is sustained but does not appear to increase further in the vast majority. Underlying CFLD should not be a barrier to treatment. Although there was a reduction in ALP when elevated at baseline, this was not unique to those with pre-existing CFLD.(c) 2023 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:256 / 262
页数:7
相关论文
共 50 条
  • [31] Longitudinal profiling of the intestinal microbiome in children with cystic fibrosis treated with elexacaftor-tezacaftor-ivacaftor
    Reasoner, Seth A.
    Bernard, Rachel
    Waalkes, Adam
    Penewit, Kelsi
    Lewis, Janessa
    Sokolow, Andrew G.
    Brown, Rebekah F.
    Edwards, Kathryn M.
    Salipante, Stephen J.
    Hadjifrangiskou, Maria
    Nicholson, Maribeth R.
    MBIO, 2024, 15 (02):
  • [32] Effects of Elexacaftor-Tezacaftor-Ivacaftor on Nasal and Sinus Symptoms in Children With Cystic Fibrosis
    Petit, Guillaume
    Coudert, Aurelie
    Hermann, Ruben
    Truy, Eric
    Bonjour, Maxime
    Reix, Philippe
    Ayari, Sonia
    PEDIATRIC PULMONOLOGY, 2025, 60 (01)
  • [33] Effect of elexacaftor/tezacaftor/ivacaftor on airway and systemic inflammation in cystic fibrosis
    Casey, Michelle
    Gabillard-Lefort, Claudie
    McElvaney, Oisin F.
    McElvaney, Oliver J.
    Carroll, Tomas
    Heeney, Ronan C.
    Gunaratnam, Cedric
    Reeves, Emer P.
    Murphy, Mark P.
    McElvaney, Noel G.
    THORAX, 2023, 78 (08) : 835 - 839
  • [34] Elexacaftor/tezacaftor/ivacaftor corrects monocyte microbicidal deficiency in cystic fibrosis
    Cavinato, Luca
    Luly, Francesco R.
    Pastore, Valentina
    Chiappetta, Daniele
    Sangiorgi, Gloria
    Ferrara, Eva
    Baiocchi, Pia
    Mandarello, Giuseppe
    Cimino, Giuseppe
    Del Porto, Paola
    Ascenzioni, Fiorentina
    EUROPEAN RESPIRATORY JOURNAL, 2023, 61 (04)
  • [35] Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Advanced Cystic Fibrosis Lung Disease
    Djavid, Amir Reza
    Thompson, Alison E.
    Irace, Alexandria L.
    Gusman, Elen
    Altman, Kimberly
    DiMango, Emily A.
    Keating, Claire L.
    ANNALS OF THE AMERICAN THORACIC SOCIETY, 2021, 18 (11) : 1924 - 1927
  • [36] Elexacaftor-tezacaftor-ivacaftor overdose in an adolescent female with cystic fibrosis
    Lyman, Benjamin C.
    Seay, Jessica
    Contreary, Casey
    Savant, Adrienne P.
    Dell, Mary Lynn
    Hescock, George C.
    PEDIATRIC PULMONOLOGY, 2022, 57 (12) : 3174 - 3176
  • [37] Characterization of sleep in emerging adults with cystic fibrosis on elexacaftor/tezacaftor/ivacaftor
    Meltzer, Lisa J.
    Gross, Jane E.
    JOURNAL OF CYSTIC FIBROSIS, 2024, 23 (01) : 132 - 136
  • [38] Characteristics of individuals with cystic fibrosis in the United States ineligible for ivacaftor and elexacaftor/tezacaftor/ivacaftor
    Sanders, Don B.
    Mayer-Hamblett, Nicole
    Rosenfeld, Margaret
    Polinieni, Deepika
    Dasenbrook, Elliott
    Szczesniak, Rhonda
    Cromwell, Elizabeth A.
    JOURNAL OF CYSTIC FIBROSIS, 2025, 24 (02) : 255 - 262
  • [39] Impact of Elexacaftor/Tezacaftor/Ivacaftor on Cystic Fibrosis Liver Tests in a Real-World Cohort with and Without Baseline CFLD
    Bowen, M.
    Sample, E.
    Collins, A.
    Singhal, A.
    Brown, A.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2021, 203 (09)
  • [40] ANALYSIS OF ACCESS TO THE FIRST FILL OF ELEXACAFTOR/TEZACAFTOR/IVACAFTOR IN PEDIATRIC AND ADULT CYSTIC FIBROSIS PATIENTS
    Burrus, T.
    Loy, S.
    Teibel, H.
    Taylor, A.
    Sorgen, P.
    Pettit, R. S.
    PEDIATRIC PULMONOLOGY, 2020, 55 : S247 - S247