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Ambrisentan therapy in pulmonary hypertension: oedema is the most common side effect leading to cessation of therapy


Ambrisentan ( US: Letairis; EU: Volibris ) is an oral selective endothelin receptor antagonist licensed for use in pulmonary arterial hypertension ( PAH ).
There are few data on clinical use and long-term tolerability in a wider range of patients with pulmonary hypertension ( PH ).

All patients treated with Ambrisentan over a 4-year period were identified. Baseline characteristics, liver function test ( LFT ) results and World Health Organization ( WHO ) functional class were retrieved from hospital databases.

272 patients received Ambrisentan during the period 2009-2013 ( 32% idiopathic PAH, 36% connective tissue disease PAH, 11% congenital heart disease PAH, 6% portopulmonary hypertension, 1% HIV PAH, 4% PH in association with lung disease, 8% chronic thromboembolic PH and 2% PH in association with sarcoidosis ).

33.5% of patients received Ambrisentan as monotherapy and 12% received Ambrisentan as their initial PH therapy. 18% stopped treatment due to side effects and 12% stopped due to lack of efficacy.

Oedema was the most common side effect leading to cessation of therapy, which occurred in 7% of patients. 57% of patients who discontinued Ambrisentan due to side effects also discontinued other pulmonary arterial hypertension therapies due to side effects previously or subsequently.

Ambrisentan was discontinued in two ( less than 1% ) patients due to abnormal liver function tests.

The 3-year survival in congenital heart disease PAH, idiopathic PAH and systemic sclerosis-associated PAH was 80%, 62%, and 38%, respectively ( p = 0.003 ).
Survival was superior in patients in whom WHO functional class improved in response to therapy.

In conclusion, Ambrisentan is used as an initial therapy and as monotherapy in a minority of patients in a large UK PH referral centre.
Discontinuation due to side effects, and especially oedema, was higher than reported in previous studies while discontinuation due to abnormal liver function tests was very uncommon.
A majority of patients who discontinued therapy due to side effects also previously or subsequently discontinued other pulmonary arterial hypertension therapies.
Improvement in WHO functional class was associated with superior survival. ( Xagena )

Condliffe R et al, Ther Adv Respir Dis 2014;8:71-77

XagenaMedicine_2014



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