Rosenkranz Stephan, Ghofrani Hossein-Ardeschir, Hoeper Marius M, Langleben David, Hegab Sara, Rahner Claudia, Richard Jean-François, McLaughlin Vallerie V
Department of Cardiology - Internal Medicine III, Heart Center, University Hospital Cologne, Cologne, Germany; Cologne Cardiovascular Research Center (CCRC), University of Cologne, Cologne, Germany.
University of Giessen and Marburg Lung Center, Member of the German Center for Lung Research (DZL), Giessen, Germany; Department of Pneumology, Kerckhoff-Klinik, Bad Nauheim, Germany; Department of Medicine, Imperial College London, London, UK.
J Heart Lung Transplant. 2025 Feb;44(2):135-146. doi: 10.1016/j.healun.2024.08.018. Epub 2024 Sep 3.
There is limited evidence to support treatment recommendations in patients with pulmonary arterial hypertension (PAH) and comorbidities. To investigate the impact of riociguat treatment in this patient population, we analyzed pooled data from randomized controlled trials of riociguat.
This post hoc analysis included data from the PATENT-1, PATENT-2, PATENT PLUS, and REPLACE studies. Safety, efficacy (6-minute walk distance [6MWD], World Health Organization functional class [WHO-FC], and N-terminal probrain natriuretic peptide [NT-proBNP]), and COMPERA 2.0 risk status were assessed in patients with 0, 1 to 2, or 3 to 4 cardiometabolic comorbidities (obesity, systemic hypertension, diabetes mellitus, coronary artery disease) in the main phase of the studies. Safety was also assessed in the long-term extensions.
The analysis included 686 patients (riociguat, n = 440; placebo, n = 132; phosphodiesterase type 5 inhibitors [PDE5i], n = 114), of whom 55%, 39%, and 6% had 0, 1 to 2, and 3 to 4 comorbidities, respectively. In the main phase, rates and severity of adverse events (AEs) were similar in riociguat-treated patients across comorbidity subgroups. After 2 years, discontinuations of riociguat due to AEs were also similar across subgroups. Compared with placebo and PDE5i, riociguat improved 6MWD and NT-proBNP across comorbidity groups and improved WHO-FC and COMPERA 2.0 risk status in patients with 0 or 1 to 2 comorbidities.
Riociguat had an acceptable safety profile in PAH patients with cardiometabolic comorbidities. Efficacy and risk assessment results suggest that riociguat can be beneficial for patients with PAH, irrespective of the presence of comorbidities.
支持肺动脉高压(PAH)合并症患者治疗建议的证据有限。为了研究利奥西呱治疗对该患者群体的影响,我们分析了利奥西呱随机对照试验的汇总数据。
这项事后分析纳入了PATENT-1、PATENT-2、PATENT PLUS和REPLACE研究的数据。在研究的主要阶段,对患有0种、1至2种或3至4种心脏代谢合并症(肥胖、系统性高血压、糖尿病、冠状动脉疾病)的患者进行安全性、疗效(6分钟步行距离[6MWD]、世界卫生组织功能分级[WHO-FC]和N末端脑钠肽前体[NT-proBNP])以及COMPERA 2.0风险状态评估。在长期延长期也评估了安全性。
分析纳入了686例患者(利奥西呱组,n = 440;安慰剂组,n = 132;5型磷酸二酯酶抑制剂[PDE5i]组,n = 114),其中分别有55%、39%和6%的患者患有0种、1至2种和3至4种合并症。在主要阶段,合并症亚组中接受利奥西呱治疗的患者不良事件(AE)发生率和严重程度相似。2年后,各亚组中因AE停用利奥西呱的情况也相似。与安慰剂和PDE5i相比,利奥西呱在各合并症组中均改善了6MWD和NT-proBNP,并改善了患有0种或1至2种合并症患者的WHO-FC和COMPERA 2.0风险状态。
利奥西呱在患有心脏代谢合并症的PAH患者中具有可接受的安全性。疗效和风险评估结果表明,无论是否存在合并症,利奥西呱对PAH患者都可能有益。