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ID 67727
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Hirai, Kenta Department of Pediatrics Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Sawada, Ryusuke Department of Pharmacology Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Hayashi, Tomohiro Department of Pediatrics Kurashiki Central Hospital
Araki, Toru Department of Pediatrics National Hospital Organization Fukuyama Medical Center
Nakagawa, Naomi Department of Pediatric Cardiology Hiroshima City Hiroshima Citizens Hospital
Kondo, Maiko Department of Pediatrics Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences
Yasuda, Kenji Department of Pediatrics Shimane University Faculty of Medicine
Hirata, Takuya Department of Pediatrics Kyoto University Graduate School of Medicine
Sato, Tomoyuki Department of Pediatrics Jichi Medical University
Nakatsuka, Yuki Department of Data Science, Center for Innovative Clinical Medicine Okayama University Hospital
Yoshida, Michihiro Department of Data Science, Center for Innovative Clinical Medicine Okayama University Hospital
Kasahara, Shingo Department of Cardiovascular Surgery Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences Kaken ID publons
Baba, Kenji Department of Pediatrics Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences ORCID Kaken ID
Oh, Hidemasa Department of Regenerative Medicine, Center for Innovative Clinical Medicine Okayama University Hospital ORCID Kaken ID researchmap
the TICAP/PERSEUS Study Group
Abstract
Background: Cardiosphere‐derived cell (CDC) infusion was associated with better clinical outcomes at 2 years in patients with single ventricle heart disease. The current study investigates time‐to‐event outcomes at 8 years.
Methods and Results: This cohort enrolled patients with single ventricles who underwent stage 2 or stage 3 palliation from January 2011 to January 2015 at 8 centers in Japan. The primary outcomes were time‐dependent CDC treatment effects on death and late complications during 8 years of follow‐up, assessed by restricted mean survival time. Among 93 patients enrolled (mean age, 2.3±1.3 years; 56% men), 40 received CDC infusion. Overall survival for CDC‐treated versus control patients did not differ at 8 years (hazard ratio [HR], 0.60 [95% CI, 0.21–1.77]; P=0.35). Treatment effect had nonproportional hazards for death favoring CDCs at 4 years (restricted mean survival time difference +0.33 years [95% CI, 0.01–0.66]; P=0.043). In patients with heart failure with reduced ejection fraction, CDC treatment effect on survival was greater over 8 years (restricted mean survival time difference +1.58 years [95% CI, 0.05–3.12]; P=0.043). Compared with control participants, CDC‐treated patients showed lower incidences of late failure (HR, 0.45 [95% CI, 0.21–0.93]; P=0.027) and adverse events (subdistribution HR, 0.50 [95% CI, 0.27–0.94]; P=0.036) at 8 years.
Conclusions: By 8 years, CDC infusion was associated with lower hazards of late failure and adverse events in single ventricle heart disease. CDC treatment effect on survival was notable by 4 years and showed a durable clinical benefit in patients with heart failure with reduced ejection fraction over 8 years.
Registration: URL: https://www.clinicaltrials.gov; Unique identifiers: NCT01273857 and NCT01829750.
Keywords
cardiosphere
heart failure
restricted mean survival time
single ventricle
survival
Published Date
2024-11-19
Publication Title
Journal of the American Heart Association
Volume
volume13
Issue
issue22
Publisher
Wiley
Start Page
e038137
ISSN
2047-9980
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2024 The Author(s).
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DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.1161/JAHA.124.038137
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Funder Name
Japan Society for the Promotion of Science
Japan Heart Foundation
Miyata Cardiac Research Promotion Foundation
助成番号
22H03040