Division of Rheumatology, Johns Hopkins University , Baltimore, MD, USA.
Division of Rheumatology, University of California , Los Angeles, CA, USA.
Expert Opin Pharmacother. 2020 Nov;21(16):2041-2056. doi: 10.1080/14656566.2020.1793960. Epub 2020 Jul 17.
Systemic sclerosis (SSc) is a multi-dimensional connective tissue disease of unknown etiology. Given the immense clinical complexity of SSc, the treatment of this condition is not standardized and considerable heterogeneity exists in SSc management approaches. The purpose of this article is to highlight novel therapeutic strategies and new medications under development for the treatment of systemic sclerosis (SSc).
Herein, the authors focus primarily on recently completed clinical trials and phase 3 and 4 clinical trials of therapeutic agents that show promise in SSc. This review is organized by the clinical complications that occur in SSc, for which novel treatment strategies are under study.
Combining therapies to address the individual manifestations of SSc is a cornerstone to the comprehensive management of this condition. Therapeutic strategies must take into account the organs involved, the level of disease activity in each area, and the disease stage. Controlling the complex biological network, progressive vasculopathy and fibrosis, as well as manifestations of end-organ dysfunction are all critical considerations when determining the best treatment approach for SSc.
系统性硬化症(SSc)是一种病因不明的多维度结缔组织疾病。鉴于 SSc 临床表现极其复杂,其治疗尚未标准化,SSc 的管理方法存在很大的异质性。本文旨在强调治疗系统性硬化症(SSc)的新治疗策略和正在开发的新药。
本文作者主要关注最近完成的临床试验以及在 SSc 中显示出前景的治疗药物的 3 期和 4 期临床试验。本综述按 SSc 中发生的临床并发症进行组织,这些并发症正在研究新的治疗策略。
联合治疗以解决 SSc 的个体表现是综合管理该疾病的基石。治疗策略必须考虑到涉及的器官、每个区域的疾病活动程度以及疾病阶段。控制复杂的生物网络、进行性血管病变和纤维化以及终末器官功能障碍的表现,都是确定 SSc 最佳治疗方法时需要考虑的关键因素。