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Table_1_Disease patterns and specific trajectories of anti-MDA5-related disease: a multicentre retrospective study of 70 adult patients.docx (14.85 kB)

Table_1_Disease patterns and specific trajectories of anti-MDA5-related disease: a multicentre retrospective study of 70 adult patients.docx

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posted on 2024-01-08, 05:00 authored by Hubert de Boysson, Marie Cuchet, Charles Cassius, Pierre Cuchet, Christian Agard, Alexandra Audemard-Verger, Sylvain Marchand-Adam, Raphaëlla Cohen-Sors, Laure Gallay, Julie Graveleau, Cécile Lesort, Kim Ly, Alain Meyer, Grégoire Monseau, Antoine Néel, Bernard Bonnotte, Laurent Pérard, Nicolas Schleinitz, Delphine Mariotte, Brigitte Le Mauff, Gwladys Bourdenet, Wafa Masmoudi, Samuel Deshayes, Anaël Dumont, Anne Dompmartin, Diane Kottler, Achille Aouba
Introduction

This study aimed to provide an updated analysis of the different prognostic trajectories of patients with anti-melanoma differentiation-associated gene 5 (MDA5) antibodies.

Methods

Among a cohort of 70 patients, baseline characteristics and phenotypes, treatments and outcomes were analyzed. A Cox proportional hazards model was used to identify factors associated with poor outcomes, i.e., death or progressive disease at the last follow-up.

Results

Among the 70 patients, 45 were women, and 54 were Caucasian. A dermatologic involvement was observed in 58 (83%) patients, including 40 with MDA5 vasculopathy-related skin lesions. Muscular involvement was observed in 39 (56%) patients. Interstitial lung disease (ILD) was observed at baseline in 52 (74%) patients, including 23 (44%) who developed rapidly progressive (RP) ILD. Seven (10%) patients showed thromboembolic complications within the first weeks of diagnosis, and eight (11%) other patients developed a malignancy (4 before the diagnosis of anti-MDA5 disease). Poor outcomes were observed in 28 (40%) patients, including 13 (19%) deaths. Among the 23 patients with RP-ILD, 19 (79%) showed poor outcomes, including 12 (63%) who died. In multivariate analyses, RP-ILD (hazard ratio (HR), 95% CI: 8.24 [3.21–22], p<0.0001), the occurrence of thromboembolic events (HR: 5.22 [1.61–14.77], p=0.008) and the presence of any malignancy (HR: 19.73 [6.67–60], p<0.0001) were the three factors independently associated with poor outcomes.

Discussion

This new independent cohort confirms the presence of different clinical phenotypes of anti-MDA5 diseases at baseline and the poor prognosis associated with RP-ILD. Thromboembolic events and malignancies were also identified as prognostic factors.

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