Oral corticosteroid dosing strategies for post-COVID-19 organising pneumonia: NORCOVID clinical trial

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Authors: David Espejo-Castellanos, Aitor González-Amezcua, María-Florencia Pilia, Antia Ferreiro-Posse, Galo Granados, Christian Romero-Mesones, Íñigo Ojanguren, Maria A. Ramon, Maria-Jesus Cruz, Xavier Muñoz, Ferran Torres, the Se-COVID-19 team
+16 more Marta Arjona, Míriam Barrecheguren, Cristina Berastegui, José Cardoso, David Clofent, Almudena Felipe, María Angeles Jiménez, Manuel Lopez, Jeisson Osorio, Mercedes Pallero, Eva María Revilla, Berta Saez, Maria Saéz, Júlia Sampol, Eduardo Vélez, Ana Villar
Cited by: 1
References: 31

Abstract

Background Organising pneumonia is an interstitial lung disease linked to infections and other conditions. Cryptogenic organising pneumonia is a rarer, idiopathic form. Organising pneumonia has become one of the most frequent respiratory complications following severe acute respiratory syndrome coronavirus 2 pneumonia. Standard treatment involves the use of glucocorticoids. The objective of the study is to determine the optimal dosage of oral corticosteroids for the treatment of this disease. Methods Randomised, open-label, assessor-blinded, parallel-group, single-centre, noninferiority clinical trial with an active control group comparing two oral prednisone regimens. The control group received prednisone 0.75 mg·kg −1 ·day −1 for 4 weeks; 0.5 mg·kg −1 ·day −1 for 4 weeks; 20 mg·day −1 for 4 weeks; 10 mg·day −1 for 6 weeks; or 5 mg·day −1 for 6 weeks (total treatment duration 6 months) and the experimental group prednisone 0.5 mg·kg −1 ·day −1 for 3 weeks; 20 mg·day −1 for 3 weeks; 15 mg·day −1 for 2 weeks; 10 mg·day −1 for 2 weeks; and 5 mg·day −1 for 2 weeks (total treatment duration 3 months). Visits were carried out at baseline and at 3, 6 and 12 months, recording clinical history, physical examination, pulmonary function tests and chest computed tomography. The primary outcome was noninferiority with a margin of 10% in diffusing capacity of the lung for carbon monoxide ( D LCO ) at 6 months. Results 79 patients were randomised according to intention-to-treat group, 40 to the experimental group and 39 to the control group. Mean± sd baseline D LCO was 59.3±16.7% in the experimental group and 55.5±16.5% in the control group, with mean improvements at 6 months of 11.7% (95% CI 7.18–16.17%) and 12.8% (95% CI 8.57–17.11%) respectively. The difference between groups at 6 months was 1.23% (95% CI −5.13–7.59%), the experimental regimen being noninferior to the control group with the margin of 10%. Patients in the experimental group had fewer than half as many adverse effects as controls: nine (23%) versus 22 (56%) (p=0.0027). Conclusions Treatment with oral corticosteroids lasting 3 months (initial dose of prednisone 0.5 mg·kg −1 ·day −1 ) may be recommended in patients with post-COVID organising pneumonia.

Fields of Study & Subjects

Long-Term Effects of COVID-19 Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis COVID-19 Clinical Research Studies

Publication details

Journal / source
ERJ Open Research
Publisher
European Respiratory Society (ERS)
Volume
12
Issue
4
Pages
01552–2025
Publication date
14 May 2026
Language
EN