4.8 Article

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

Journal

CIRCULATION
Volume 125, Issue 2, Pages 324-334

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCULATIONAHA.110.016667

Keywords

cardiopulmonary exercise; clinical trials; pediatrics; pulmonary arterial hypertension; sildenafil

Funding

  1. Pfizer Inc.
  2. Gilead
  3. United Therapeutics
  4. Pfizer
  5. Actelion
  6. Bayer
  7. Ikaria

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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.

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