The efficacy and safety of systemic corticosteroids as first line treatment for granulomatous lymphocytic interstitial lung disease.
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Smits, BasGoldacker, 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
Publication date
2022-12-29
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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.2022.12.813Type
ArticleAdditional Links
http://www.sciencedirect.com/science/journal/00916749PMID
36587851Publisher
Mosbyae974a485f413a2113503eed53cd6c53
10.1016/j.jaci.2022.12.813