Why the study?
Bosentan and sildenafil are commonly combined for pulmonary arterial hypertension, but evidence indicates a significant drug interaction between them.
Does transitioning from bosentan and sildenafil to alternative therapy maintain clinical stability and safety in patients with pulmonary arterial hypertension?
Does transitioning from bosentan and sildenafil to alternative therapy maintain clinical stability and safety in patients with pulmonary arterial hypertension?
Transitioning patients with pulmonary arterial hypertension from the combination of bosentan and sildenafil to alternative therapies is safe and maintains clinical stability.
Transitioning PAH patients from bosentan-sildenafil may be feasible; leaves open need for prospective trials of alternatives.
The combination of bosentan and sildenafil is commonly used to treat patients with pulmonary arterial hypertension (PAH); however, there is evidence of a significant drug interaction between these two medications. We sought to evaluate the safety and efficacy of transitioning patients with PAH from the combination of bosentan and sildenafil to alternative therapy. A retrospective database review was performed on 16 patients with PAH who were treated with the combination of bosentan and sildenafil and transitioned to alternative treatment at our center. Invasive and non-invasive patient parameters were collected at baseline and after transition. 56.3% of patients were in World Health Organization functional class (WHO FC) III and a majority of patients (68.7%) were on background prostacyclin therapy. The most common reason for transition was concern for a drug interaction in seven patients (43.8%). The most common transition was bosentan to macitentan in eight patients (50%). Fifteen patients (93.8%) tolerated the transition after a median follow-up of 6.5 months with minor adverse events occurring in four patients (25%). In 11 patients, 6-min walk distance (6MWD) was unchanged comparing baseline to post transition measurements with a median change of +8 m (range: -50 to + 70; P = 0.39). Nine patients (81.8%) had stable (within 15% margin) or significant improvement (increase by ≥15%) in 6MWD after transition. All patients demonstrated stable or improved WHO FC after transition. There were no significant changes after transition in hemodynamics, N-terminal pro-brain natriuretic peptide (NT-proBNP) values, or Registry to Evaluate Early and Long-Term PAH Disease Management (REVEAL) risk scores. In our study, transitioning patients from bosentan and sildenafil to alternative therapy was safe and resulted in clinical stability.
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Verlinden et al. (2020) studied this question.
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