Division of Pulmonary and Critical Care Medicine, School of Medicine, Oregon Health and Science University, Portland, OR, USA.
Division of Pulmonary & Critical Care Medicine and the Mary M. Parkes Center, University of Rochester Medical Center, Rochester, NY, USA.
Respir Med. 2022 Mar;193:106744. doi: 10.1016/j.rmed.2022.106744. Epub 2022 Jan 19.
Oral treprostinil has been shown to improve exercise capacity and delay disease progression in patients with pulmonary arterial hypertension (PAH), but its effects on hemodynamics are not well-characterized. The FREEDOM-EV trial was a Phase III, international, placebo-controlled, double-blind, event-driven study in 690 participants with PAH who were taking a single oral PAH therapy. FREEDOM-EV demonstrated a significantly reduced risk for clinical worsening with oral treprostinil taken three times daily and did not uncover new safety signals in PAH patients. Sixty-one participants in the FREEDOM-EV trial volunteered for a hemodynamics sub-study. Pulmonary artery compliance (PAC), a ratio of stroke volume to pulmonary pulse pressure, significantly increased from Baseline to Week 24 in the oral treprostinil group compared with the placebo group (geometric mean 26.4% active vs. -6.0% placebo; ANCOVA p=0.007). There was a significant increase in cardiac output in the oral treprostinil group compared to the placebo group (geometric mean 11.3% active vs. -6.4% placebo; ANCOVA p=0.005) and a corresponding significant reduction in pulmonary vascular resistance (PVR) (geometric mean -21.5 active vs. -1.8% placebo; ANCOVA p=0.02) from Baseline to Week 24. These data suggest that increased compliance contributes to the physiological mechanism by which oral treprostinil improves exercise capacity and delays clinical worsening for patients with PAH.
口服曲前列尼尔已被证明可改善肺动脉高压(PAH)患者的运动能力并延缓疾病进展,但它对血液动力学的影响尚未得到很好的描述。FREEDOM-EV 试验是一项在 690 名接受单一口服 PAH 治疗的 PAH 患者中进行的 III 期、国际、安慰剂对照、双盲、事件驱动研究。FREEDOM-EV 表明,与安慰剂相比,每日口服三次曲前列尼尔可显著降低临床恶化风险,并且在 PAH 患者中未发现新的安全性信号。FREEDOM-EV 试验中有 61 名参与者自愿参加了血液动力学子研究。与安慰剂组相比,口服曲前列尼尔组的肺动脉顺应性(PAC),即每搏量与肺动脉脉搏压的比值,从基线到第 24 周显著增加(几何均数 26.4%活跃 vs. -6.0%安慰剂;ANCOVA p=0.007)。与安慰剂组相比,口服曲前列尼尔组的心输出量显著增加(几何均数 11.3%活跃 vs. -6.4%安慰剂;ANCOVA p=0.005),相应地,肺血管阻力(PVR)显著降低(几何均数 -21.5 活跃 vs. -1.8%安慰剂;ANCOVA p=0.02)从基线到第 24 周。这些数据表明,顺应性的增加有助于解释口服曲前列尼尔改善运动能力和延缓 PAH 患者临床恶化的生理机制。