[Systemic sclerosis-related interstitial lung disease: Diagnostic and therapeutic strategy in the light of recent clinical trials] - Université de Rennes Accéder directement au contenu
Article Dans Une Revue La Revue de Médecine Interne Année : 2022

[Systemic sclerosis-related interstitial lung disease: Diagnostic and therapeutic strategy in the light of recent clinical trials]

Résumé

Systemic sclerosis (SSc) is an autoimmune disease associated to fibrotic manifestations. Interstitial lung disease (SSc-ILD), one of the main fibrotic features of SSc, is the first cause of SSc-related death. The management of SSc-ILD has recently benefited from the results of key randomised controlled trials. French authorities have approved Nintedanib for the treatment of SSc-ILD, and tocilizumab has recently been approved by the Food and Drug Administration (FDA) in the United-States (US). These recent approvals challenge the management of this fibrotic manifestation of SSc. This narrative literature review, at the crossroad of internal medicine and pulmonology, discusses what could be an up-to date approach, in terms of diagnostic and therapeutic strategies for SSc-ILD, in the light of the results from recent clinical trials.

Dates et versions

hal-03610735 , version 1 (16-03-2022)

Identifiants

Citer

A Lescoat, S Jouneau, Y Uzunhan, P Jégo, Vincent Cottin, et al.. [Systemic sclerosis-related interstitial lung disease: Diagnostic and therapeutic strategy in the light of recent clinical trials]. La Revue de Médecine Interne, 2022, 43 (6), pp.365-374. ⟨10.1016/j.revmed.2021.12.003⟩. ⟨hal-03610735⟩
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