Jaïs Xavier, D'Armini Andrea M, Jansa Pavel, Torbicki Adam, Delcroix Marion, Ghofrani Hossein A, Hoeper Marius M, Lang Irene M, Mayer Eckhard, Pepke-Zaba Joanna, Perchenet Loïc, Morganti Adele, Simonneau Gérald, Rubin Lewis J
Antoine Béclère Hospital, Clamart, France.
J Am Coll Cardiol. 2008 Dec 16;52(25):2127-34. doi: 10.1016/j.jacc.2008.08.059.
Our goal was to investigate the effect of treatment with the oral dual endothelin receptor antagonist bosentan on the hemodynamics and exercise capacity of patients with chronic thromboembolic pulmonary hypertension (CTEPH).
CTEPH is characterized by vascular obstruction and remodeling, leading to increased pulmonary vascular resistance (PVR). Although pulmonary endarterectomy (PEA) is potentially curative, medical therapy is needed in patients with inoperable disease or persistent/recurrent pulmonary hypertension after PEA.
The BENEFiT (Bosentan Effects in iNopErable Forms of chronIc Thromboembolic pulmonary hypertension) study was a double-blind, randomized, placebo-controlled study in CTEPH including patients with either inoperable CTEPH or persistent/recurrent pulmonary hypertension after PEA (>6 months after PEA). Independent coprimary end points were change in PVR as a percentage of baseline and change from baseline in 6-min walk distance after 16 weeks of treatment with bosentan or placebo. Secondary end points included change from baseline in World Health Organization functional class and other hemodynamic parameters.
One hundred fifty-seven patients were enrolled and randomized: 80 to placebo, 77 to bosentan. A statistically significant treatment effect (TE) of bosentan over placebo on PVR was demonstrated: -24.1% of baseline (95% confidence interval [CI]: -31.5% to -16.0%; p < 0.0001). Total pulmonary resistance (TE: -193 dynxsxcm(-5); 95% CI: -283 to -104 dyn.s.cm(-5); p < 0.0001) and cardiac index (TE: 0.3 lxmin(-1)xm(-2); 95% CI: 0.14 to 0.46 lxmin(-1)xm(-2); p = 0.0007) improved. Mean TE on 6-min walk distance was +2.2 m (95% CI: -22.5 to 26.8 m; p = 0.5449). Bosentan treatment was well tolerated.
This study demonstrated a positive TE of bosentan on hemodynamics in this patient population. No improvement was observed in exercise capacity. Further trials are needed to define the role of medical therapy in patients with CTEPH (Bosentan Effects in Inoperable Forms of Chronic Thromboembolic Pulmonary Hypertension; NCT00313222).
我们的目标是研究口服双重内皮素受体拮抗剂波生坦治疗对慢性血栓栓塞性肺动脉高压(CTEPH)患者血流动力学和运动能力的影响。
CTEPH的特征是血管阻塞和重塑,导致肺血管阻力(PVR)增加。尽管肺动脉内膜剥脱术(PEA)可能治愈疾病,但对于无法手术的患者或PEA术后持续性/复发性肺动脉高压的患者仍需要药物治疗。
BENEFiT(波生坦对无法手术的慢性血栓栓塞性肺动脉高压形式的影响)研究是一项针对CTEPH患者的双盲、随机、安慰剂对照研究,包括无法手术的CTEPH患者或PEA术后(PEA术后>6个月)持续性/复发性肺动脉高压患者。独立的共同主要终点是治疗16周后PVR相对于基线的变化百分比以及6分钟步行距离相对于基线的变化。次要终点包括世界卫生组织功能分级和其他血流动力学参数相对于基线的变化。
157例患者入组并随机分组:80例接受安慰剂,77例接受波生坦。波生坦相对于安慰剂对PVR的治疗效果(TE)具有统计学意义:为基线的-24.1%(95%置信区间[CI]:-31.5%至-16.0%;p<0.0001)。总肺阻力(TE:-193dyn·s·cm⁻⁵;95%CI:-283至-104dyn·s·cm⁻⁵;p<0.0001)和心脏指数(TE:0.3L·min⁻¹·m⁻²;95%CI:0.14至0.46L·min⁻¹·m⁻²;p = 0.0007)得到改善。6分钟步行距离的平均TE为+2.2m(95%CI:-22.5至26.8m;p = 0.5449)。波生坦治疗耐受性良好。
本研究证明波生坦对该患者群体的血流动力学具有积极的治疗效果。未观察到运动能力的改善。需要进一步试验来确定药物治疗在CTEPH患者中的作用(波生坦对无法手术的慢性血栓栓塞性肺动脉高压形式的影响;NCT00313222)。