Effect of allogeneic adipose tissue derived mesenchymal stromal cell treatment in chronic ischemic heart failure with reduced ejection fraction – The SCIENCE Trial

Research output: Contribution to journalJournal articleResearchpeer-review

  • Bas Van Klarenbosch
  • Sabina Frljak
  • Andraz Cerar
  • Gregor Poglajen
  • Denise Traxler‐weidenauer
  • Pawel Nadrowski
  • Christina Paitazoglou
  • Bojan Vrtovec
  • Martin W. Bergmann
  • Steven A.j. Chamuleau
  • Wojtek Wojakowski
  • Mariann Gyöngyösi
  • Adriaan Kraaijeveld
  • Kristian Schultz Hansen
  • Erik Jørgensen
  • Steffen Helqvist
  • Francis Richard Joshi
  • Ellen Mønsted Johansen
  • Morten Juhl
  • Lisbeth Drozd Højgaard
  • Anders Bruun Mathiasen
  • Annette Ekblond
  • Mandana Haack‐sørensen
  • Jens Kastrup
Aims
The aim of the SCIENCE trial was to investigate whether a single treatment with direct intramyocardial injections of adipose tissue-derived mesenchymal stromal cells (CSCC_ASCs) was safe and improved cardiac function in patients with chronic ischaemic heart failure with reduced ejection fraction (HFrEF).

Methods and results
The study was a European multicentre, double-blind, placebo-controlled phase II trial using allogeneic CSCC_ASCs from healthy donors or placebo (2:1 randomization). Main inclusion criteria were New York Heart Association (NYHA) class II–III, left ventricular ejection fraction (LVEF) <45%, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels >300 pg/ml. CSCC_ASCs or placebo (isotonic saline) were injected directly into viable myocardium. The primary endpoint was change in left ventricular end-systolic volume (LVESV) at 6-month follow-up measured by echocardiography. A total of 133 symptomatic HFrEF patients were included. The treatment was safe without any drug-related severe adverse events or difference in cardiac-related adverse events during a 3-year follow-up period. There were no significant differences between groups during follow-up in LVESV (0.3 ± 5.0 ml, p = 0.945), nor in secondary endpoints of left ventricular end-diastolic volume (−2.0 ± 6.0 ml, p = 0.736) and LVEF (−1.6 ± 1.0%, p = 0.119). The NYHA class improved slightly within the first year in both groups without any difference between groups. There were no changes in 6-min walk test, NT-proBNP, C-reactive protein or quality of life the first year in any groups.

Conclusion
The SCIENCE trial demonstrated safety of intramyocardial allogeneic CSCC_ASC therapy in patients with chronic HFrEF. However, it was not possible to improve the pre-defined endpoints and induce restoration of cardiac function or clinical symptoms.
Original languageEnglish
JournalEuropean Journal of Heart Failure
Volume25
Issue number4
Pages (from-to)576-587
Number of pages12
ISSN1567-4215
DOIs
Publication statusPublished - 2023

ID: 332609957