Bosentan for Treatment of Inoperable Chronic Thromboembolic Pulmonary Hypertension

被引:443
作者
Jais, Xavier [1 ]
D'Armini, Andrea M. [2 ]
Jansa, Pavel [3 ]
Torbicki, Adam [4 ]
Delcroix, Marion [5 ]
Ghofrani, Hossein A. [6 ]
Hoeper, Marius M. [7 ]
Lang, Irene M. [8 ]
Mayer, Eckhard [9 ]
Pepke-Zaba, Joanna [10 ]
Perchenet, Loic [11 ]
Morganti, Adele [11 ]
Simonneau, Gerald
Rubin, Lewis J. [12 ]
机构
[1] Hop Antoine Beclere, Serv Pneumol & Reanimat Resp, F-92140 Clamart, France
[2] Univ Pavia, Sch Med, St Matteo Hosp, Div Cardiac Surg, I-27100 Pavia, Italy
[3] Charles Univ Prague, Fac Med 1, Dept Med 2, Clin Dept Cardiol & Angiol, Prague, Czech Republic
[4] Inst TB & Lung Dis, Dept Chest Med, Warsaw, Poland
[5] Univ Hosp Gasthuisberg, Dept Pulmonol, B-3000 Leuven, Belgium
[6] Univ Giessen, Lung Ctr, Giessen, Germany
[7] Hannover Med Sch, D-3000 Hannover, Germany
[8] Med Univ Vienna, Vienna, Austria
[9] Catholic Acad Hosp, Mainz, Germany
[10] Papworth Hosp, Cambridge CB3 8RE, England
[11] Actel Pharmaceut Ltd, Allschwil, Switzerland
[12] Univ Calif San Diego, La Jolla, CA 92093 USA
关键词
pulmonary endarterectomy; bosentan; operability; hemodynamics;
D O I
10.1016/j.jacc.2008.08.059
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives 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). Background 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. Methods 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. Results 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 dyn.s.cm(-5); 95% CI: -283 to -104 dyn.s.cm(-5); p < 0.0001) and cardiac index (TE: 0.3 I.min(-1).m(-2); 95% CI: 0.14 to 0.46 I.min (1).m (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. Conclusions 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). (J Am Coll Cardiol 2008; 52: 2127-34) (C) 2008 by the American College of Cardiology Foundation
引用
收藏
页码:2127 / 2134
页数:8
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