Impact of different sequential triple oral combination therapies based selexipag on outcomes in pulmonary arterial hypertension

Author:

Hu Xiaoyi1ORCID,Yuan Ping1,Chen Jun2,Wang Shang1,Zhao Hui1,Wei Yaqin1,Fu Jiaqi1,Chen Fadong3,Ruan Hongyun4,Zhang Wei5,Zhou Yanli6,Wang Qiqi7ORCID,Xu Xiaoling8,Feng Kefu9,Guo Jianzhou10,Gong Sugang1,Zhang Ruifeng11,Zhao Qinhua1,Wang Lan1

Affiliation:

1. Department of Pulmonary Circulation, Shanghai Pulmonary Hospital, School of Medicine Tongji University Shanghai China

2. Department of Cardiology Xiamen Hospital of Traditional Chinese Medicine Fujian China

3. Department of Cardiology, Tongji Hospital Tongji University School of Medicine Shanghai China

4. Department of Cardiology Xuzhou Central Hospital Xuzhou China

5. Department of Rheumatology, Renji Hospital Shanghai Jiaotong University School of Medicine Shanghai China

6. Department of Cardiology First Affiliated Hospital of Nanjing Medical University Nanjing China

7. Department of Cardiology and Atrial Fibrillation Center, The First Affiliated Hospital College of Medicine Zhejiang University Hangzhou Zhejiang China

8. Department of Pulmonary and Critical Care Medicine, Sir Run Run Shaw Hospital Zhejiang University School of Medicine Hangzhou China

9. Department of Cardiology, Division of Life Sciences and Medicine, The First Affiliated Hospital of USTC University of Science and Technology of China Hefei Anhui China

10. Fuwai Hospital Chinese Academy of Medical Sciences Shenzhen Guangdong Province China

11. Department of Respiratory Medicine Zhongda Hospital of Southeast University Nanjing China

Abstract

AbstractBackgroundWhile the GRIPHON study and others have confirmed the efficacy and safety of selexipag with single, dual, and initial triple combination therapy for patients with pulmonary arterial hypertension (PAH), multicenters studies concerning diverse triple oral combination therapies based on selexipag are limited.HypothesisThis study was conducted to evaluate the effects of various sequential triple oral combination therapies on PAH outcomes.MethodsA retrospective study was carried out involving 192 patients from 10 centers, who were receiving sequential triple oral combination therapy consisting of an endothelin receptor antagonist (ERA), a phosphodiesterase 5 inhibitor (PDE5i)/riociguat and selexipag. Clinical parameters, event‐free survival, and all‐cause survival were assessed and analyzed at baseline and posttreatment.ResultsAmong the 192 patients, 37 were treated with ERA + riociguat + selexipag, and 155 patients received ERA + PDE5i + selexipag. Both sequential triple oral combination therapies improved the World Health Organization functional class and raised the count of low‐risk parameters. As a result of the larger patients' population in the ERA + PDE5i + selexipag group, these individuals exhibited significant increases in 6‐minute walking distance (6MWD), pulmonary arterial systolic pressure, pulmonary arterial pressure, right ventricle, and eccentricity index, and significant decreases in N‐terminal probrain natriuretic peptide after 6 months of treatment. Nevertheless, both sequential triple oral combination therapy groups demonstrated similar shifts in these clinical parameters between baseline and 6 months. Baseline 6MWD and mean pulmonary arterial pressure were independent predictors of survival in patients undergoing ERA + PDE5i + selexipag therapy. Importantly, no significant differences were found in 6‐month event‐free survival and all‐cause survival between two groups.ConclusionsDifferent oral sequential triple combination therapies based on selexipag could comparably improve outcomes in patients with PAH.

Funder

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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