Xu Linrui, Wang Faping, Luo Fengming
Department of Pulmonary and Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Laboratory of Pulmonary Immunology and Inflammation, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Front Pharmacol. 2022 Oct 28;13:1019915. doi: 10.3389/fphar.2022.1019915. eCollection 2022.
Interstitial lung disease (ILD) is a common pulmonary disease often associated with significant morbidity and mortality in patients with connective tissue diseases (CTD). Currently, no gold-standard therapies are available for CTD-ILD. Recently, several studies have proposed that rituximab (RTX) may be effective for the treatment of CTD-ILD. This study aimed to systematically evaluate the efficacy and safety of RTX for the treatment of CTD-ILD. Studies were selected from PubMed, Embase, and Cochrane Library, up to 20 July 2022. Improvement and stable rates were extracted as the main outcomes and pooled using the weighted mean proportion with fixed or random-effects models, in case of significant heterogeneity ( > 50%). Safety analysis was performed based on the adverse events reported in all of the studies. Thirteen studies (312 patients) were included in the meta-analysis. The follow-up durations ranged from 6 to 36 months. The pooled improvement rate was 35.0% (95% CI: 0.277-0.442), while the pooled stable rate was 59.2% (95% CI: 0.534-0.656). Anti-synthetase syndrome associated with ILD [ASS-ILD, 48.1% (95% CI, 0.373-0.620)] and idiopathic inflammatory myopathies associated with ILD [IIM-ILD, non-ASS, 47.4% (95% CI, 0.266-0.846)] had higher improvement rates than the other types. A total of 106 adverse events associated with RTX or progressive ILD were reported among the 318 patients, 55.7% of which were mild. Among 19 deaths, 17 were due to ILD progression, one to severe pulmonary arterial hypertension, and one to infection. RTX, which exhibits a satisfactory safety profile, is an effective treatment option for CTD-ILD, even in patients who fail to respond to other therapies. Further randomized trials are needed to assess the efficacy of rituximab compared to other treatments for CTD-ILD. PROSPERO, identifier (CRD42022363403).
间质性肺疾病(ILD)是一种常见的肺部疾病,在结缔组织病(CTD)患者中常伴有显著的发病率和死亡率。目前,尚无针对CTD-ILD的金标准治疗方法。最近,多项研究提出利妥昔单抗(RTX)可能对CTD-ILD的治疗有效。本研究旨在系统评价RTX治疗CTD-ILD的疗效和安全性。研究选取截至2022年7月20日的PubMed、Embase和Cochrane图书馆的数据。提取改善率和稳定率作为主要结局指标,若存在显著异质性(I²>50%),则采用固定效应模型或随机效应模型合并加权平均比例。基于所有研究报告的不良事件进行安全性分析。荟萃分析纳入了13项研究(312例患者)。随访时间为6至36个月。合并改善率为35.0%(95%CI:0.277-0.442),合并稳定率为59.2%(95%CI:0.534-0.656)。与ILD相关的抗合成酶综合征[ASS-ILD,48.1%(95%CI,0.373-0.620)]和与ILD相关的特发性炎性肌病[IIM-ILD,非ASS,47.4%(95%CI,0.266-0.846)]的改善率高于其他类型。318例患者中共报告了106例与RTX或进行性ILD相关的不良事件,其中55.7%为轻度。19例死亡病例中,17例死于ILD进展,1例死于严重肺动脉高压,1例死于感染。RTX具有令人满意的安全性,是CTD-ILD的有效治疗选择,即使是对其他治疗无反应的患者。需要进一步的随机试验来评估利妥昔单抗与其他治疗CTD-ILD方法相比的疗效。国际前瞻性系统评价注册库(PROSPERO),标识符(CRD42022363403)。