任天堂
医学
美罗华
肺科医生
间质性肺病
托珠单抗
内科学
重症监护医学
痹症科
临床试验
疾病
特发性肺纤维化
肿瘤科
肺
淋巴瘤
作者
Elisabetta Zanatta,Beatrice Moccaldi,Gabriella Szücs,Paolo Spagnolo
标识
DOI:10.1016/j.autrev.2023.103463
摘要
Systemic sclerosis (SSc) is a heterogeneous autoimmune disease, where a significant proportion of patients develop interstitial lung disease (ILD), which is the major cause of mortality. In recent years, the diagnosis of SSc-ILD has improved a lot, and caring rheumatologists, together with pulmonologists, regularly screen and follow the development and course of ILD. Considerable progress has also been made in the treatment of SSc-ILD based on several clinical trials. The recommendations for immunosuppressive treatment have been modified and supplemented with targeted agents (tocilizumab, rituximab), and antifibrotic drugs such as nintedanib registered as a new treatment for SSc-ILD. However, there are no clear recommendations regarding the start and timing of nintedanib treatment. A debate on the early introduction of nintenadib or not took place on the 7th edition of the International Congress on Controversies in Rheumatology and Autoimmunity (CORA) in March/2023, and this review summarizes the main arguments that were discussed in this session.
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