Riociguat for pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension: Results from a phase II long-term extension study

被引:32
作者
Halank, Michael [1 ]
Hoeper, Marius M. [2 ,3 ]
Ghofrani, Hossein-Ardeschir [3 ,4 ,5 ]
Meyer, F. Joachim [6 ]
Staehler, Gerd [7 ]
Behr, Juergen [3 ,8 ,9 ]
Ewert, Ralf [10 ]
Fletcher, Monique [11 ]
Colorado, Pablo [12 ]
Nikkho, Sylvia [13 ]
Grimminger, Friedrich [3 ,4 ]
机构
[1] Univ Hosp Carl Gustav Carus, Med Clin Pneumol 1, Dresden, Germany
[2] Hannover Med Sch, Clin Resp Med, Hannover, Germany
[3] German Ctr Lung Res DZL, Giessen, Germany
[4] UGMLC, Giessen, Germany
[5] Imperial Coll London, Dept Med, London, England
[6] Univ Hosp, Dept Cardiol & Resp Med, Heidelberg, Germany
[7] Loewenstein Clin gGmbH, Med Clin 1, Loewenstein, Germany
[8] Univ Munich, Dept Internal Med 5, Munich, Germany
[9] Asklepios Fachklin Munich Gauting, Munich, Germany
[10] Ernst Moritz Arndt Univ Greifswald, Clin Internal Med B, Greifswald, Germany
[11] Bayer PLC, Global Clin Dev, Newbury, Berks, England
[12] Bayer Pharma AG, Global Clin Dev, Parsippany, NJ USA
[13] Bayer Pharma AG, Global Clin Dev, Berlin, Germany
关键词
Clinical study; Pulmonary hypertension; Soluble guanylate cyclase stimulator; Riociguat; INTERNATIONAL PROSPECTIVE REGISTRY; OPEN-LABEL; OUTCOMES; PREDICTORS; HEMOPTYSIS; TRIAL;
D O I
10.1016/j.rmed.2017.05.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Riociguat was well tolerated and improved exercise and functional capacity in patients with pulmonary arterial hypertension (PAH) and inoperable chronic thromboembolic pulmonary hypertension (CTEPH) in a 12 -week Phase II trial. We present final data from the long-term extension phase of this study. Methods: During this multicenter, open-label, uncontrolled long-term extension study, riociguat dose could be changed at the physician's discretion (range 0.5-2.5 mg three times daily). The primary outcome was long-term safety and tolerability of riociguat; secondary outcomes included 6-minute walking distance, World Health Organization functional class, survival, and clinical worsening-free survival. Results: Sixty-eight patients (inoperable CTEPH, n = 41; PAH, n = 27) entered the long-term extension. Median treatment duration at the final data cut-off was 77 months. The most common adverse events were nasopharyngitis (57%) and peripheral edema (37%). Three patients (4%) experienced serious adverse events of hemoptysis: two moderate, one severe, none fatal or considered drug-related. At Month 48, 6-minute walking distace increased from baseline by 69 +/- 105 m, and World Health Organization functional class improved/stabilized/worsened versus baseline in 50/45/5% of patients. Three-year survival and clinical worsening-free survival were 91% and 49%, respectively (with patients censored if they withdrew without experiencing an event). Starting a new PAH treatment was the most frequent clinical worsening event. Conclusions: Improvements in exercise and functional capacity were maintained at 4 years in patients remaining on treatment, with no new safety signals identified. These data support riociguat as a long-term treatment option for PAH and inoperable CTEPH. Trial registered at: ClinicalTrials.gov. Registration number: NCT00454558. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:50 / 56
页数:7
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