Literature DB >> 36204579

Selexipag-based triple combination therapy improves prognosis in Chinese pulmonary arterial hypertension patients.

Xiaopei Cui1, Weida Lu1, Deyuan Zhang2, Liangyi Qie1, Haijun Li1, Xiao Li1, Hui Liu3, Qiushang Ji4.   

Abstract

Aim: Selexipag is an oral selective prostacyclin receptor agonist approved for treatment of patients with pulmonary arterial hypertension (PAH). In the present study, we aim to assess the safety and efficacy of selexipag in triple combination therapy with endothelial receptor antagonists (ERAs) and PDE5is for Chinese PAH patients. Methods and results: A single center retrospective study was performed on group 1 PAH patients (n = 68) initiating triple combination therapy with selexipag from 1 February 2020 to 31 August 2021 in Qilu Hospital of Shandong University (Shandong, China). Adolescents, children, and PAH patients with unrepaired congenital heart disease were excluded. The French pulmonary hypertension network (FPHN) non-invasive risk assessment, echocardiogram parameters, and clinical data, including tolerability, safety, and death/hospitalization events associated with PAH, were collected. Of the 68 patients, 31 (45.6%) patients had tolerable side effects while only a single patient discontinued selexipag due to severe diarrhea. In the analysis of the efficacy set of 62 patients, the median selexipag treatment time from selexipag initiation to last risk assessment was 27 (21, 33) weeks. Compared to baseline parameters, the percentage of WHO FC III/IV decreased from 77.4% (48) to 24.2% (15) (p = 0.000), median 6-min walk distance (6MWD) increased 82 m [from 398 (318, 450) to 480 (420, 506) m; p = 0.000], and NT-proBNP levels decreased from 1,216 (329, 2,159) to 455 (134, 1,678) pg/mL (p = 0.007). Patients who improved to three low-risk criteria increased from 9.7 to 38.7%. Right ventricular diameter (RV) diameter also decreased and was accompanied by an improved tricuspid annular plane systolic excursion (TAPSE). Patients transitioning from subcutaneous treprostinil to selexipag continued to show improvements in WHO FC, 6MWD (404 ± 94 vs. 383 ± 127 m) and NT-proBNP levels (2,319 ± 2,448 vs. 2,987 ± 3,770 pg/mL). Finally, the 1-year event free survival rate was 96.7% for patients initiating the triple combination therapy within 3 years of PAH diagnosis.
Conclusion: Triple combination therapy with selexipag was safe and effective in Chinese PAH patients, which was confirmed by acceptable tolerability, and improved exercise capacity, right heart function, risk assessment, and prognosis.
Copyright © 2022 Cui, Lu, Zhang, Qie, Li, Li, Liu and Ji.

Entities:  

Keywords:  pulmonary arterial hypertension; risk assessment; selexipag; tolerability; triple combination

Year:  2022        PMID: 36204579      PMCID: PMC9530145          DOI: 10.3389/fcvm.2022.991586

Source DB:  PubMed          Journal:  Front Cardiovasc Med        ISSN: 2297-055X


  30 in total

1.  Real-life data on Selexipag for the treatment of pulmonary hypertension.

Authors:  Michaela Barnikel; Nikolaus Kneidinger; Friederike Klenner; Andrea Waelde; Paola Arnold; Torben Sonneck; Jürgen Behr; Claus Neurohr; Katrin Milger
Journal:  Pulm Circ       Date:  2019 Jan-Mar       Impact factor: 3.017

2.  Initial combination therapy with ambrisentan and tadalafil and mortality in patients with pulmonary arterial hypertension: a secondary analysis of the results from the randomised, controlled AMBITION study.

Authors:  Marius M Hoeper; Vallerie V McLaughlin; Joan Albert Barberá; Adaani E Frost; Hossein-Ardeschir Ghofrani; Andrew J Peacock; Gérald Simonneau; Stephan Rosenkranz; Ronald J Oudiz; R James White; Karen L Miller; Jonathan Langley; Julia H N Harris; Christiana Blair; Lewis J Rubin; Jean-Luc Vachiery
Journal:  Lancet Respir Med       Date:  2016-10-11       Impact factor: 30.700

3.  Hemodynamics and risk assessment 2 years after the initiation of upfront ambrisentan‒tadalafil in pulmonary arterial hypertension.

Authors:  Michele D'Alto; Roberto Badagliacca; Francesco Lo Giudice; Paola Argiento; Gavino Casu; Marco Corda; Michele Correale; Stefano Ghio; Alessandra Greco; Mariangela Lattanzio; Valentina Mercurio; Giuseppe Paciocco; Silvia Papa; Renato Prediletto; Emanuele Romeo; Maria Giovanna Russo; Alessandro Tayar; Patrizio Vitulo; Carmine Dario Vizza; Paolo Golino; Robert Naeije
Journal:  J Heart Lung Transplant       Date:  2020-08-28       Impact factor: 10.247

4.  Risk assessment in pulmonary arterial hypertension.

Authors:  Marius M Hoeper; David Pittrow; Christian Opitz; J Simon R Gibbs; Stephan Rosenkranz; Ekkehard Grünig; Karen M Olsson; Doerte Huscher
Journal:  Eur Respir J       Date:  2018-03-29       Impact factor: 16.671

5.  Riociguat for the treatment of pulmonary arterial hypertension.

Authors:  Hossein-Ardeschir Ghofrani; Nazzareno Galiè; Friedrich Grimminger; Ekkehard Grünig; Marc Humbert; Zhi-Cheng Jing; Anne M Keogh; David Langleben; Michael Ochan Kilama; Arno Fritsch; Dieter Neuser; Lewis J Rubin
Journal:  N Engl J Med       Date:  2013-07-25       Impact factor: 91.245

6.  A comprehensive risk stratification at early follow-up determines prognosis in pulmonary arterial hypertension.

Authors:  David Kylhammar; Barbro Kjellström; Clara Hjalmarsson; Kjell Jansson; Magnus Nisell; Stefan Söderberg; Gerhard Wikström; Göran Rådegran
Journal:  Eur Heart J       Date:  2018-12-14       Impact factor: 29.983

7.  Continuous subcutaneous infusion of treprostinil, a prostacyclin analogue, in patients with pulmonary arterial hypertension: a double-blind, randomized, placebo-controlled trial.

Authors:  Gerald Simonneau; Robyn J Barst; Nazzareno Galie; Robert Naeije; Stuart Rich; Robert C Bourge; Anne Keogh; Ronald Oudiz; Adaani Frost; Shelmer D Blackburn; James W Crow; Lewis J Rubin
Journal:  Am J Respir Crit Care Med       Date:  2002-03-15       Impact factor: 21.405

Review 8.  Selexipag in Pulmonary Arterial Hypertension: Most Updated Evidence From Recent Preclinical and Clinical Studies.

Authors:  Raktim K Ghosh; Somedeb Ball; Avash Das; Dhrubajyoti Bandyopadhyay; Samhati Mondal; Debjit Saha; Anjan Gupta
Journal:  J Clin Pharmacol       Date:  2016-12-21       Impact factor: 3.126

9.  Patient and disease characteristics of the first 500 patients with pulmonary arterial hypertension treated with selexipag in real-world settings from SPHERE.

Authors:  Nick H Kim; Anna R Hemnes; Murali M Chakinala; Kristin B Highland; Kelly M Chin; Vallerie McLaughlin; Carol Zhao; Veena Narayan; Harrison W Farber
Journal:  J Heart Lung Transplant       Date:  2021-01-15       Impact factor: 10.247

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