A Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study of Oral Sildenafil Citrate in Treatment-Naive Children With Pulmonary Arterial Hypertension

被引:271
|
作者
Barst, Robyn J. [1 ]
Ivy, D. Dunbar [2 ,3 ]
Gaitan, Guillermo [4 ]
Szatmari, Andras [5 ]
Rudzinski, Andrzej [6 ]
Garcia, Alberto E. [7 ]
Sastry, B. K. S. [8 ]
Pulido, Tomas [9 ]
Layton, Gary R. [10 ]
Serdarevic-Pehar, Marjana [10 ]
Wessel, David L. [11 ]
机构
[1] Columbia Univ, New York, NY USA
[2] Univ Colorado, Sch Med, Dept Pediat, Aurora, CO USA
[3] Childrens Hosp Colorado, Aurora, CO USA
[4] UNICAR, Dept Pediat Cardiol, Guatemala City, Guatemala
[5] Gottsegen Gyorgy Hungarian Inst Cardiol, Dept Pediat Cardiol, Budapest, Hungary
[6] Jagiellonian Univ, Krakow, Poland
[7] Fdn Cardioinfantil, Bogota, Colombia
[8] CARE Hosp, Dept Cardiol, Hyderabad, Andhra Pradesh, India
[9] Inst Nacl Cardiol, Cardiopulm Dept, Mexico City, DF, Mexico
[10] Pfizer Ltd, Pfizer Worldwide Pharmaceut Operat, Sandwich CT13 9NJ, Kent, England
[11] Childrens Natl Med Ctr, Washington, DC 20010 USA
关键词
cardiopulmonary exercise; clinical trials; pediatrics; pulmonary arterial hypertension; sildenafil; 6-MINUTE WALK TEST; PEDIATRIC-PATIENTS; CLINICAL-EFFICACY; HEART-FAILURE; THERAPY; BOSENTAN; SIZE; GENETICS; REGISTRY; DISEASE;
D O I
10.1161/CIRCULATIONAHA.110.016667
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Safe, effective therapy is needed for pediatric pulmonary arterial hypertension. Methods and Results-Children (n = 235; weight >8 kg) were randomized to low-, medium-, or high-dose sildenafil or placebo orally 3 times daily for 16 weeks in the Sildenafil in Treatment-Naive Children, Aged 1-17 Years, With Pulmonary Arterial Hypertension (STARTS-1) study. The primary comparison was percent change from baseline in peak oxygen consumption (P(V)over dot(O2)) for the 3 sildenafil doses combined versus placebo. Exercise testing was performed in 115 children able to exercise reliably; the study was powered for this population. Secondary end points (assessed in all patients) included hemodynamics and functional class. The estimated mean +/- SE percent change in P(V)over dot(O2) for the 3 doses combined versus placebo was 7.7 +/- 4.0% (95% confidence interval, -0.2% to 15.6%; P = 0.056). P(V)over dot(O2), functional class, and hemodynamics improved with medium and high doses versus placebo; low-dose sildenafil was ineffective. Most adverse events were mild to moderate in severity. STARTS-1 completers could enter the STARTS-2 extension study; patients who received sildenafil in STARTS-1 continued the same dose, whereas placebo-treated patients were randomized to low-, medium-, or high-dose sildenafil. In STARTS-2 (ongoing), increased mortality was observed with higher doses. Conclusions-Sixteen-week sildenafil monotherapy is well tolerated in pediatric pulmonary arterial hypertension. Percent change in P(V)over dot(O2) for the 3 sildenafil doses combined was only marginally significant; however, P(V)over dot(O2), functional class, and hemodynamic improvements with medium and high doses suggest efficacy with these doses. Combined with STARTS-2 data, the overall profile favors the medium dose. Further investigation is warranted to determine optimal dosing based on age and weight.
引用
收藏
页码:324 / 334
页数:11
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