Effect of transition from sitaxsentan to ambrisentan in pulmonary arterial hypertension
- PMID: 21468170
- PMCID: PMC3064451
- DOI: 10.2147/VHRM.S15026
Effect of transition from sitaxsentan to ambrisentan in pulmonary arterial hypertension
Abstract
Introduction: Currently available endothelin receptor antagonists for treating pulmonary arterial hypertension block either the endothelin (ET) receptor A or both A and B receptors. Transition from one endothelin receptor antagonist to another may theoretically alter side-effects or efficacy. We report our experience of a transition from sitaxsentan to ambrisentan, both predominant ET(A) receptor antagonists, in pulmonary arterial hypertension patients.
Methods: At Baylor Pulmonary Hypertension Center, 18 patients enrolled in the open-label extension phase of the original sitaxsentan studies (Sitaxsentan To Relieve ImpaireD Exercise) were transitioned to ambrisentan (from July 2007 to September 2007) at the time of study closure. Pre-transition (PreT), 1 month (1Mth) and 1 year (1Yr) post-transition assessments of 6-minute walk distance (6MWD), brain naturetic peptide (BNP) levels, WHO functional class (WHO FC), Borg dyspnea score (BDS), oxygen saturation, liver function, and peripheral edema were compared.
Results: 6MWD was 356 ± 126 m at PreT, 361 ± 125 m at 1Mth, and 394 ± 114 m at 1Yr (mean ± SD). There was no difference in the walk distance at 1Mth and 1Yr post transition compared with PreT (P=0.92, 0.41 respectively). Oxygen saturation was no different at 1Mth and 1Yr to PreT level (P=0.49 and P=0.06 respectively). BNP was 178 ± 44 pg/mL at PreT, 129 ± 144 pg/mL at 1Mth and 157 ± 201 at 1Yr. Peripheral edema was present in 7/18 patients at PreT, in 8/16 patients at 1Mth, and in 6/13 patients at 1Yr post transition. Proportions of patients with edema over these 3 time points did not change significantly (P=0.803). At 1Yr, 2 patients had died, 1 had undergone lung transplantation, 1 had relocated, and 1 patient was started on intravenous prostacyclin therapy. Over 3 points (baseline, 1 month, and 1 year), there was no significant change in function class (P=0.672).
Conclusion: Our limited data suggest that ET(A) receptor antagonists can be switched from one to another with sustained exercise capacity and maintained WHO FC with no increase in incidence of peripheral edema.
Keywords: 6-minute walk distance; echocardiogram; endothelial receptor antagonist; right heart failure.
© 2011 Safdar, publisher and licensee Dove Medical Press Ltd.
Figures





Similar articles
-
STRIDE 1: effects of the selective ET(A) receptor antagonist, sitaxsentan sodium, in a patient population with pulmonary arterial hypertension that meets traditional inclusion criteria of previous pulmonary arterial hypertension trials.J Cardiovasc Pharmacol. 2004 Nov;44 Suppl 1:S80-4. doi: 10.1097/01.fjc.0000166207.74178.d0. J Cardiovasc Pharmacol. 2004. PMID: 15838366 Clinical Trial.
-
Evaluation of efficacy, safety and tolerability of Ambrisentan in Chinese adults with pulmonary arterial hypertension: a prospective open label cohort study.BMC Cardiovasc Disord. 2016 Oct 22;16(1):201. doi: 10.1186/s12872-016-0361-9. BMC Cardiovasc Disord. 2016. PMID: 27770771 Free PMC article. Clinical Trial.
-
Frequency of edema in patients with pulmonary arterial hypertension receiving ambrisentan.Am J Cardiol. 2012 Nov 1;110(9):1373-7. doi: 10.1016/j.amjcard.2012.06.040. Epub 2012 Aug 2. Am J Cardiol. 2012. PMID: 22858181 Free PMC article. Clinical Trial.
-
Ambrisentan for the management of pulmonary arterial hypertension.Clin Ther. 2008 May;30(5):825-33. doi: 10.1016/j.clinthera.2008.05.005. Clin Ther. 2008. PMID: 18555930 Review.
-
Ambrisentan: a review of its use in pulmonary arterial hypertension.Ther Adv Respir Dis. 2017 Jun;11(6):233-244. doi: 10.1177/1753465817696040. Epub 2017 Apr 20. Ther Adv Respir Dis. 2017. PMID: 28425346 Free PMC article. Review.
Cited by
-
Management Considerations for Pulmonary Arterial Hypertension Pharmacotherapy in the Intensive Care Unit.Pharmacy (Basel). 2023 Sep 13;11(5):145. doi: 10.3390/pharmacy11050145. Pharmacy (Basel). 2023. PMID: 37736917 Free PMC article. Review.
-
Transition from Ambrisentan to Bosentan in Pulmonary Arterial Hypertension: A Single-Center Prospective Study.Can Respir J. 2018 Apr 11;2018:9836820. doi: 10.1155/2018/9836820. eCollection 2018. Can Respir J. 2018. PMID: 29849836 Free PMC article.
-
Endothelin antagonists for diabetic and non-diabetic chronic kidney disease.Br J Clin Pharmacol. 2013 Oct;76(4):573-9. doi: 10.1111/bcp.12064. Br J Clin Pharmacol. 2013. PMID: 23228194 Free PMC article. Review.
-
EXPRESS: Switching to riociguat: A potential treatment strategy for the management of CTEPH and PAH.Pulm Circ. 2019 Feb 26;10(1):2045894019837849. doi: 10.1177/2045894019837849. Online ahead of print. Pulm Circ. 2019. PMID: 30803329 Free PMC article.
-
The Transition From Ambrisentan to Macitentan in Patients With Pulmonary Arterial Hypertension: A Real-word Prospective Study.Front Pharmacol. 2022 Jan 12;12:811700. doi: 10.3389/fphar.2021.811700. eCollection 2021. Front Pharmacol. 2022. PMID: 35095523 Free PMC article.
References
-
- Rubin LJ. Pathology and pathophysiology of primary pulmonary hypertension. Am J Cardiol. 1995;75(3):51A–54A. - PubMed
-
- Safdar Z. Targeted oral therapies in the treatment of pulmonary arterial hypertension. Clin Drug Investig. 2010;30(12):811–826. - PubMed
-
- Valerio CJ, Kabunga P, Coghlan JG. Safety and efficacy of ambrisentan in the treatment of pulmonary arterial hypertension. Clin Med Ther. 2009;1:541–556.
-
- Wu C, Chan MF, Stavros F, et al. Discovery of TBC11251, a potent, long acting, orally active endothelin receptor-A selective antagonist. J Med Chem. 1997;40(11):1690–1697. - PubMed
-
- Wu C, Decker ER, Blok N, et al. Endothelin antagonists: substituted mesitylcarboxamides with high potency and selectivity for ET(A) receptors. J Med Chem. 1999;42(22):4485–4499. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical