Tucker Torry A, Komissarov Andrey A, Idell Steven
Department of Cellular and Molecular Biology, School of Medicine, The University of Texas Health Science Center at Tyler, 11937 US HWY 271, Tyler, TX, 70708, USA.
Respir Res. 2025 Mar 18;26(1):105. doi: 10.1186/s12931-025-03184-y.
Intrapleural fibrinolytic therapy (IPFT), also known as intrapleural enzymatic therapy (IET), has been utilized for decades to treat pleural infections by expediting drainage in patients with pleural organization. The successful MIST2 trial demonstrated that IPFT improves pleural opacification, reduces hospital stays, and decreases short-term surgical referrals. Despite significant progress, gaps remain in identification of the optimal fibrinolytic agents, dosing, and safety improvements. IPFT is generally recommended for patients with loculation and failed pleural drainage, with a consensus panel advocating for combined tissue plasminogen activator (tPA) and DNase therapy. How each agent may affect the activity or function of the other in the combination remains unclear. While IPFT can reduce the need for surgical intervention, there are relatively few comparative clinical trials to guide initial therapy. Emerging low-dose IPFT treatment approaches may benefit patients who are poor surgical candidates. Personalized IPFT candidate approaches, such as the Fibrinolytic Potential Assay (FPA), could refine dosing and improve outcomes. Additionally, biomarkers like pleural fluid PAI-1 and suPAR concentrations may predict clinical outcomes and guide treatment. New therapeutic agents, including PAI-1 inhibiting peptides and mesothelial profibrogenic targets, are under investigation to enhance IPFT efficacy. These advances hold promise for improving the management of pleural infections and other forms of pleural organization.
胸膜内纤维蛋白溶解疗法(IPFT),也称为胸膜内酶疗法(IET),数十年来一直被用于通过加快胸膜粘连患者的引流来治疗胸膜感染。成功的MIST2试验表明,IPFT可改善胸膜浑浊,缩短住院时间,并减少短期手术转诊。尽管取得了重大进展,但在确定最佳纤维蛋白溶解剂、剂量和安全性改善方面仍存在差距。IPFT通常推荐用于有包裹性积液和胸膜引流失败的患者,一个共识小组主张联合使用组织纤溶酶原激活剂(tPA)和脱氧核糖核酸酶治疗。在联合治疗中,每种药物如何影响另一种药物的活性或功能仍不清楚。虽然IPFT可以减少手术干预的需求,但相对较少的比较临床试验来指导初始治疗。新兴的低剂量IPFT治疗方法可能使手术候选不佳的患者受益。个性化的IPFT候选方法,如纤维蛋白溶解潜力测定(FPA),可以优化剂量并改善治疗效果。此外,诸如胸膜液PAI-1和suPAR浓度等生物标志物可能预测临床结果并指导治疗。包括PAI-1抑制肽和间皮促纤维化靶点在内的新型治疗药物正在研究中,以提高IPFT的疗效。这些进展有望改善胸膜感染和其他形式胸膜粘连的管理。