Vacchi Caterina, Sebastiani Marco, Cassone Giulia, Cerri Stefania, Della Casa Giovanni, Salvarani Carlo, Manfredi Andreina
PhD Program in Clinical and Experimental Medicine, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Rheumatology Unit, University of Modena and Reggio Emilia, Azienda Ospedaliero-Universitaria Policlinico di Modena, 41121 Modena, Italy.
J Clin Med. 2020 Feb 3;9(2):407. doi: 10.3390/jcm9020407.
Interstitial lung disease (ILD) is one of the most serious pulmonary complications of connective tissue diseases (CTDs) and it is characterized by a deep impact on morbidity and mortality. Due to the poor knowledge of CTD-ILD's natural history and due to the difficulties related to design of randomized control trials, there is a lack of prospective data about the prevalence, follow-up, and therapeutic efficacy. For these reasons, the choice of therapy for CTD-ILD is currently very challenging and still largely based on experts' opinion. Treatment is often based on steroids and conventional immunosuppressive drugs, but the recent publication of the encouraging results of the INBUILD trial has highlighted a possible effective and safe use of antifibrotic drugs as a new therapeutic option for these subjects. Aim of this review is to summarize the available data and recent advances about therapeutic strategies for ILD in the context of various CTD, such as systemic sclerosis, idiopathic inflammatory myopathy and Sjogren syndrome, systemic lupus erythematosus, mixed connective tissue disease and undifferentiated connective tissue disease, and interstitial pneumonia with autoimmune features, focusing also on ongoing clinical trials.
间质性肺疾病(ILD)是结缔组织病(CTD)最严重的肺部并发症之一,其特点是对发病率和死亡率有深远影响。由于对CTD-ILD自然史了解不足,以及与随机对照试验设计相关的困难,缺乏关于患病率、随访和治疗效果的前瞻性数据。由于这些原因,目前CTD-ILD的治疗选择极具挑战性,且很大程度上仍基于专家意见。治疗通常基于类固醇和传统免疫抑制药物,但最近公布的INBUILD试验的令人鼓舞的结果突出了抗纤维化药物作为这些患者新治疗选择的可能有效且安全的应用。本综述的目的是总结在各种CTD背景下,如系统性硬化症、特发性炎性肌病和干燥综合征、系统性红斑狼疮、混合性结缔组织病和未分化结缔组织病以及具有自身免疫特征的间质性肺炎中,关于ILD治疗策略的现有数据和最新进展,同时也关注正在进行的临床试验。