Key result
Tadalafil yields a ~24 meter numerical increase in 6MWD compared to placebo in pediatric PAH.
Why the study?
The efficacy and safety of tadalafil in pediatric patients with pulmonary arterial hypertension added to endothelin receptor antagonist therapy were not well established.
Does tadalafil improve six-minute walk distance in pediatric patients with pulmonary arterial hypertension?
RCT (n=35)
double-blind
randomized
Yes
Does tadalafil improve six-minute walk distance in pediatric patients with pulmonary arterial hypertension?
Tadalafil showed a positive trend in improving six-minute walk distance in pediatric patients with pulmonary arterial hypertension, though the study was underpowered for statistical significance.
Supports potential add-on tadalafil benefit in pediatric PAH on ERA; leaves open definitive efficacy pending larger trials.
This study evaluated the efficacy and safety of tadalafil in pediatric patients with pulmonary arterial hypertension. This phase‐3, international, randomized, multicenter (24 weeks double‐blind placebo‐controlled period; two‐year, open‐labeled extension period), add‐on (patient’s current endothelin receptor antagonist therapy) study included pediatric patients aged <18 years with pulmonary arterial hypertension. Patients received tadalafil 20 mg or 40 mg based on their weight (heavy‐weight: ≥40 kg; middle‐weight: ≥25 to <40 kg) or placebo orally once daily for 24 weeks. Primary endpoint was change from baseline in six‐minute walk distance in patients aged ≥6 years at Week 24. Sample size was amended from 134 to ≥34 patients, due to serious recruitment challenges. Therefore, statistical significance testing was not performed between treatment groups. Results showed that patient demographics and baseline characteristics ( N = 35; tadalafil = 17; placebo = 18) were comparable between treatment groups; median age was 14.2 years (6.2–17.9 years) and majority (71.4%, n = 25) of patients were in the heavy‐weight cohort. Least square mean (standard error) changes from baseline in six‐minute walk distance at Week 24 was numerically greater with tadalafil versus placebo (60.48 (20.41) vs 36.60 (20.78) meters; placebo‐adjusted mean difference (standard deviation) 23.88 (29.11)). Safety of tadalafil treatment was as expected without any new safety concerns. During study Period 1, two patients (one in each group) discontinued due to investigator’s reported clinical worsening, and no deaths were reported. In conclusion, the statistical significance testing was not performed between the treatment groups due to low sample size; however, the study results show positive trend in improvement in non‐invasive measurements, commonly utilized by clinicians to evaluate the disease status for children with pulmonary arterial hypertension. Safety of tadalafil treatment was as expected without any new safety signals.
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Ivy et al. (2021) conducted an RCT in pulmonary arterial hypertension (n=35). tadalafil vs. placebo was evaluated on change from baseline in six-minute walk distance in patients aged ≥6 years at Week 24 (MD 23.88). Tadalafil resulted in a numerically greater change in six-minute walk distance compared to placebo (mean difference 23.88 meters) in pediatric pulmonary arterial hypertension.
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