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    The efficacy and safety of systemic corticosteroids as first line treatment for granulomatous lymphocytic interstitial lung disease.

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    Author
    Smits, Bas
    Goldacker, Sigune
    Seneviratne, Suranjith
    Malphettes, Marion
    Longhurst, Hilary
    Mohamed, Omar E
    Witt-Rautenberg, Carla
    Leeman, Lucy
    Schwaneck, Eva
    Raymond, Isabelle
    Meghit, Kilifa
    Uhlmann, Annette
    Winterhalter, Christine
    van Montfrans, Joris
    Klima, Marion
    Workman, Sarita
    Fieschi, Claire
    Lorenzo, Lorena
    Boyle, Sonja
    Onyango-Odera, Shamin
    Price, Suzanne
    Schmalzing, Marc
    Aurillac, Valerie
    Prasse, Antje
    Hartmann, Ieneke
    Meerburg, Jennifer J
    Kemner-van de Corput, Mariette
    Tiddens, Harm
    Grimbacher, Bodo
    Kelleher, Peter
    Patel, Smita Y
    Korganow, Anne-Sophie
    Viallard, Jean-Francois
    Tony, Hans-Peter
    Bethune, Claire
    Schulze-Koops, Hendrik
    Witte, Torsten
    Huissoon, Aarnoud
    Baxendale, Helen
    Grigoriadou, Sofia
    Oksenhendler, Eric
    Burns, Siobhan O
    Warnatz, Klaus
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    Publication date
    2022-12-29
    Subject
    Respiratory medicine
    Pharmacology
    
    Metadata
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    Abstract
    Background: Granulomatous and lymphocytic interstitial lung disease (gl-ILD) is a major cause of morbidity and mortality among patients with common variable immunodeficiency. Corticosteroids are recommended as first-line treatment for gl-ILD, but evidence for their efficacy is lacking. Objectives: This study analyzed the effect of high-dose corticosteroids (≥0.3 mg/kg prednisone equivalent) on gl-ILD, measured by high-resolution computed tomography (HRCT) scans, and pulmonary function test (PFT) results. Methods: Patients who had received high-dose corticosteroids but no other immunosuppressive therapy at the time (n = 56) and who underwent repeated HRCT scanning or PFT (n = 39) during the retrospective and/or prospective phase of the Study of Interstitial Lung Disease in Primary Antibody Deficiency (STILPAD) were included in the analysis. Patients without any immunosuppressive treatment were selected as controls (n = 23). HRCT scans were blinded, randomized, and scored using the Hartman score. Differences between the baseline and follow-up HRCT scans and PFT were analyzed. Results: Treatment with high-dose corticosteroids significantly improved HRCT scores and forced vital capacity. Carbon monoxide diffusion capacity significantly improved in both groups. Of 18 patients, for whom extended follow-up data was available, 13 achieved a long-term, maintenance therapy independent remission. All patients with relapse were retreated with corticosteroids, but only one-fifth of them responded. Two opportunistic infections were found in the corticosteroid treatment group, while overall infection rate was similar between cohorts. Conclusions: Induction therapy with high-dose corticosteroids improved HRCT scans and PFT results of patients with gl-ILD and achieved long-term remission in 42% of patients. It was not associated with major side effects. Low-dose maintenance therapy provided no benefit and efficacy was poor in relapsing disease. Keywords: CVID; Granulomatous and lymphocytic interstitial lung disease; Hartmann score; corticosteroids; gl-ILD; immune dysregulation; observational trial; pulmonary function tests; quality of life.
    Citation
    Smits, B., Goldacker, S., Seneviratne, S., Malphettes, M., Longhurst, H., Mohamed, O. E., Witt-Rautenberg, C., Leeman, L., Schwaneck, E., Raymond, I., Meghit, K., Uhlmann, A., Winterhalter, C., van Montfrans, J., Klima, M., Workman, S., Fieschi, C., Lorenzo, L., Boyle, S., Onyango-Odera, S., … Warnatz, K. (2023). The efficacy and safety of systemic corticosteroids as first line treatment for granulomatous lymphocytic interstitial lung disease. The Journal of allergy and clinical immunology, 152(2), 528–537. https://doi.org/10.1016/j.jaci.2022.12.813
    Type
    Article
    Handle
    http://hdl.handle.net/20.500.14200/2235
    Additional Links
    http://www.sciencedirect.com/science/journal/00916749
    DOI
    10.1016/j.jaci.2022.12.813
    PMID
    36587851
    Journal
    Journal of Allergy and Clinical Immunology
    Publisher
    Mosby
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.jaci.2022.12.813
    Scopus Count
    Collections
    Respiratory

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