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Cardiopoietic cell therapy for advanced ischaemic heart failure: results at 39 weeks of the prospective, randomized, double blind, sham-controlled CHART-1 clinical trial.

dc.contributor.authorBartunek, Jozef
dc.contributor.authorTerzic, Andre
dc.contributor.authorDavison, Beth A
dc.contributor.authorFilippatos, Gerasimos S
dc.contributor.authorRadovanovic, Slavica
dc.contributor.authorBeleslin, Branko
dc.contributor.authorMerkely, Bela
dc.contributor.authorMusialek, Piotr
dc.contributor.authorWojakowski, Wojciech
dc.contributor.authorAndreka, Peter
dc.contributor.authorHorvath, Ivan G
dc.contributor.authorKatz, Amos
dc.contributor.authorDolatabadi, Dariouch
dc.contributor.authorEl Nakadi, Badih
dc.contributor.authorArandjelovic, Aleksandra
dc.contributor.authorEdes, Istvan
dc.contributor.authorSeferovic, Petar M
dc.contributor.authorObradovic, Slobodan
dc.contributor.authorVanderheyden, Marc
dc.contributor.authorJagic, Nikola
dc.contributor.authorPetrov, Ivo
dc.contributor.authorAtar, Shaul
dc.contributor.authorHalabi, Majdi
dc.contributor.authorGelev, Valeri L
dc.contributor.authorShochat, Michael K
dc.contributor.authorKasprzak, Jaroslaw D
dc.contributor.authorSanz-Ruiz, Ricardo
dc.contributor.authorHeyndrickx, Guy R
dc.contributor.authorNyolczas, Noémi
dc.contributor.authorLegrand, Victor
dc.contributor.authorGuédès, Antoine
dc.contributor.authorHeyse, Alex
dc.contributor.authorMoccetti, Tiziano
dc.contributor.authorFernandez-Aviles, Francisco
dc.contributor.authorJimenez-Quevedo, Pilar
dc.contributor.authorBayes-Genis, Antoni
dc.contributor.authorHernandez-Garcia, Jose Maria
dc.contributor.authorRibichini, Flavio
dc.contributor.authorGruchala, Marcin
dc.contributor.authorWaldman, Scott A
dc.contributor.authorTeerlink, John R
dc.contributor.authorGersh, Bernard J
dc.contributor.authorPovsic, Thomas J
dc.contributor.authorHenry, Timothy D
dc.contributor.authorMetra, Marco
dc.contributor.authorHajjar, Roger J
dc.contributor.authorTendera, Michal
dc.contributor.authorBehfar, Atta
dc.contributor.authorAlexandre, Bertrand
dc.contributor.authorSeron, Aymeric
dc.contributor.authorStough, Wendy Gattis
dc.contributor.authorSherman, Warren
dc.contributor.authorCotter, Gad
dc.contributor.authorWijns, William
dc.contributor.authorCHART Program
dc.date.accessioned2023-01-25T09:42:45Z
dc.date.available2023-01-25T09:42:45Z
dc.date.issued2017
dc.description.abstractCardiopoietic cells, produced through cardiogenic conditioning of patients' mesenchymal stem cells, have shown preliminary efficacy. The Congestive Heart Failure Cardiopoietic Regenerative Therapy (CHART-1) trial aimed to validate cardiopoiesis-based biotherapy in a larger heart failure cohort. This multinational, randomized, double-blind, sham-controlled study was conducted in 39 hospitals. Patients with symptomatic ischaemic heart failure on guideline-directed therapy (n = 484) were screened; n = 348 underwent bone marrow harvest and mesenchymal stem cell expansion. Those achieving > 24 million mesenchymal stem cells (n = 315) were randomized to cardiopoietic cells delivered endomyocardially with a retention-enhanced catheter (n = 157) or sham procedure (n = 158). Procedures were performed as randomized in 271 patients (n = 120 cardiopoietic cells, n = 151 sham). The primary efficacy endpoint was a Finkelstein-Schoenfeld hierarchical composite (all-cause mortality, worsening heart failure, Minnesota Living with Heart Failure Questionnaire score, 6-min walk distance, left ventricular end-systolic volume, and ejection fraction) at 39 weeks. The primary outcome was neutral (Mann-Whitney estimator 0.54, 95% confidence interval [CI] 0.47-0.61 [value > 0.5 favours cell treatment], P = 0.27). Exploratory analyses suggested a benefit of cell treatment on the primary composite in patients with baseline left ventricular end-diastolic volume 200-370 mL (60% of patients) (Mann-Whitney estimator 0.61, 95% CI 0.52-0.70, P = 0.015). No difference was observed in serious adverse events. One (0.9%) cardiopoietic cell patient and 9 (5.4%) sham patients experienced aborted or sudden cardiac death. The primary endpoint was neutral, with safety demonstrated across the cohort. Further evaluation of cardiopoietic cell therapy in patients with elevated end-diastolic volume is warranted.
dc.identifier.doi10.1093/eurheartj/ehw543
dc.identifier.essn1522-9645
dc.identifier.pmcPMC5381596
dc.identifier.pmid28025189
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381596/pdf
dc.identifier.unpaywallURLhttps://academic.oup.com/eurheartj/article-pdf/38/9/648/24120989/ehw543.pdf
dc.identifier.urihttp://hdl.handle.net/10668/10715
dc.issue.number9
dc.journal.titleEuropean heart journal
dc.journal.titleabbreviationEur Heart J
dc.language.isoen
dc.organizationHospital Universitario Virgen de la Victoria
dc.page.number648-660
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeRandomized Controlled Trial
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectCardiopoiesis
dc.subjectCardiovascular disease
dc.subjectDisease severity
dc.subjectMarker
dc.subjectPrecision medicine
dc.subjectRegenerative medicine
dc.subjectStem cell
dc.subjectTarget population
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshDouble-Blind Method
dc.subject.meshFemale
dc.subject.meshHeart Failure
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMesenchymal Stem Cell Transplantation
dc.subject.meshMiddle Aged
dc.subject.meshMyocardial Ischemia
dc.subject.meshProspective Studies
dc.subject.meshTreatment Outcome
dc.subject.meshYoung Adult
dc.titleCardiopoietic cell therapy for advanced ischaemic heart failure: results at 39 weeks of the prospective, randomized, double blind, sham-controlled CHART-1 clinical trial.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number38
dspace.entity.typePublication

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